<h1 style="text-align: center;"><strong>Job Title: Quality Engineer</strong></h1><p><strong><em><u>For immediate consideration, please email your resume and interview availability to (dabarron@actalentservices.com) ASAP today or tomorrow. I am conducting interviews this week and looking to hire immediately.</u></em></strong></p><h2>Job Description</h2><p>Ensure the correct use of advanced quality planning and engineering to enhance quality, reliability, and acceptance of systems, processes, and products. Provide a professional level of quality customer service to both internal and external customers and suppliers.</p><p><br></p><h2>Responsibilities</h2><ul><li>Monitor the performance of product quality and reliability systems.</li><li>Assist and coordinate Automotive Industry Action Group (AIAG) disciplines such as Advanced Product Quality Planning (APQP), Process Control Plan (PCP), Process Failure Mode &amp; Effect Analysis (PFMEA), Process Flow Chart (PFC), Statistical Process Control (SPC), Measurement System Analysis (MSA) / Gage Repeatability &amp; Reproducibility (GR&amp;R), Metrology Inspection Methods and Strategies, Production Part Approval Process (PPAP), and Problem Solving using the 8-D and 3 Why methodology.</li><li>Generate and maintain accurate documentation relating to quality, reliability, and process.</li><li>Implement prevention/detection systems to eliminate problems affecting quality and reliability.</li><li>Prepare and present PPM (parts per million) reports, cost of quality reports, and other metrics reports.</li><li>Develop and implement quality programs, including tracking, analyzing, reporting, and problem-solving.</li><li>File all Quality paperwork accurately, including customer complaints, control plans, quality alerts, and weekly logs.</li><li>Take an active part in training and helping others as required and participate in continuous improvement teams.</li><li>Participate in pre-production activities as a quality representative.</li><li>Complete Quality System audits of supplier on-site, follow-up audit, and corrective action.</li><li>Issue supplier non-conformance and follow-up corrective action, and problem-solving with suppliers.</li><li>Coordinate Management Review process.</li><li>Assist in supplier evaluations for on-site audits.</li><li>Provide support for Quality Assurance Manager.</li><li>Use a computer to accurately enter all company-required information for data collection.</li><li>Safely operate all required lifting/moving devices.</li><li>Attend all company-specified training as required.</li><li>Participate in continual improvement.</li><li>Maintain a clean and organized work area.</li><li>Comply with Safety Expectations.</li><li>Ensure regular and punctual attendance at work.</li><li>Comply with relevant policies, procedures, and instructions, including Code of Conduct.</li><li>Occasional travel may be required.</li></ul><h2>Essential Skills</h2><ul><li>Quality engineering expertise.</li><li>Proficiency in blueprint reading and GD&amp;T interpretation.</li><li>Experience with ISO 9001 and IATF16949 documentation systems.</li><li>ASQ or CQE certification.</li><li>AIAG Disciplines proficiency.</li><li>BS in Engineering or other technical discipline.</li><li>Minimum 8 years of experience in a Quality Department within a manufacturing environment.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>ASQ Certified Quality Engineer (CQE) preferred.</li><li>Experience in the automotive industry is preferred.</li><li>Basic understanding of performing dimensional inspections of metallic components using standard metrology equipment such as calipers, micrometers, pin gages, height gages, and indicators.</li><li>Experience with CMMs, Keyence Vision Systems, or similar equipment is preferred.</li></ul><h2>Work Environment</h2><p>This role may require occasional travel and involves working in a manufacturing environment. The position demands regular and punctual attendance, adherence to safety expectations, and compliance with company policies and procedures. The work area should be maintained clean and organized at all times.</p>

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Quality Engineer

<h1><strong>Job Title: Quality Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a dedicated Quality Engineer to serve as the primary Quality representative on the MRO line, collaborating closely with operations, engineering, and customers to ensure the highest standards of quality are met.</p><p><br></p><h2>Responsibilities</h2><ul><li>Lead and support root cause investigations, FRACAS management, corrective actions, and nonconformance management.</li><li>Gather, analyze, and present data to identify trends and risks using proficient Excel skills, including pivot tables, VLOOKUPs, and filters.</li><li>Ensure issues are resolved quickly and effectively, escalating when necessary and following through to closure.</li><li>Adapt to evolving situations, confidently make decisions, and convey ownership.</li></ul><h2>Essential Skills</h2><ul><li>Quality engineering and root cause analysis.</li><li>Experience with AS9100, aerospace inspection practices, and RCCA methodologies such as 8D and 5-Whys.</li><li>Proficiency in Excel at an intermediate to advanced level.</li><li>Ability to communicate effectively across various functions and levels, from technicians to leadership.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>3+ years of experience in aerospace or defense manufacturing, preferably in an MRO environment.</li><li>J-STD, IPC-610 certifications (current or previous) are a plus.</li><li>Exposure to ERP systems like SAP and Manufacturing Execution Systems such as Siemens MES or Factory Logix.</li><li>Advanced data analysis skills using tools like PowerBI and SQL.</li></ul><h2>Work Environment</h2><p>This position operates on the first shift, typically from 8 AM to 5 PM, with flexibility to start at 7 AM. </p>

<h1 style="font-weight: 700;">Job Title: Quality Engineer</h1><br><h2>Job Description</h2><p>The Quality Engineer will focus on containment both for customers and internally, collaborating closely with production supervisors to address and resolve issues through root cause analysis. They will work alongside Manufacturing Engineers to devise poka-yokes and long-term solutions. The role supports all plant areas, including Gears, Assembly, and Components/Machining. The Quality Engineer will manage PPAP processes plant-wide, responsible for launching and approving plant moves. They will validate equipment and machines during launches, ensuring readiness for submission.</p><br><h2>Responsibilities</h2><ul><li>Facilitate PPAP processes across the plant.</li><li>Ensure quality containment.</li><li>Recommend quality improvements by identifying and applying relevant statistical methods to manufacturing processes.</li><li>Research statistical confidence by determining sample size, acceptable error rate, and levels of confidence.</li><li>Analyze quality data from plant processes and customer indicators.</li><li>Provide feedback to customers based on quality projects like warranty and APQP issues.</li><li>Lead quality investigations and problem-solving efforts.</li><li>Research statistical reliability using techniques such as mean time before failure, reliability modeling, and reliability demonstration tests.</li><li>Develop quality improvement experiments using full and fractional factorial techniques.</li><li>Create sampling plans using attribute, variable, and sequential sampling methods.</li><li>Maintain statistical process controls by applying zone charting and charts for distributions.</li><li>Analyze data using hypothesis, normal distribution, and process capability analysis tests.</li><li>Prepare statistical information and reports by collecting, analyzing, and summarizing data and trends.</li><li>Contribute to organizational success by welcoming diverse requests and assisting others in achieving job results.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor&#39;s Degree in Mechanical Engineering.</li><li>3+ years of Quality Engineering experience in a manufacturing environment.</li><li>Experience facilitating PPAP and APQP.</li><li>IATF/automotive experience.</li><li>Proven troubleshooting and root cause analysis (8D or Shainin).</li><li>Experience in capability studies.</li><li>Containment experience.</li><li>Familiarity with Six Sigma, Minitab, statistical analysis, and statistical process control.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Minitab/statistical analysis experience is a plus.</li><li>Six Sigma Black Belt certification is advantageous.</li><li>Experience with Statistical Process Control (SPC).</li></ul><h2>Work Environment</h2><p>The Quality Engineer will work primarily on the 1st shift, collaborating with a team of 14 Quality Engineers divided into Gears, Assembly, and Components (Machining) areas. The role may require travel up to 20%, primarily to facilities in Rochester, IN, and Detroit. The workweek is typically 50 hours, with standard hours from 7am-4pm or 8am-5pm. The role is approximately 60% on the floor and 40% desk-based. The team fosters a collaborative mentality, working together to address and resolve issues. Team members will have opportunities for internal training and development, with potential for career advancement. Benefits include 10 days of PTO, 6 paid holidays, and access to Udemy after 6 months.</p><br>

<h1><strong>Job Title: Quality Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>A metal stamping company in West Michigan that supports the furniture and commercial hardware industry is seeking a Quality Engineer to enhance their team. </p><p>The role involves supporting 8Ds and APQP activities, including developing PPAP packages, creating PFMEAs and control plans, running 8Ds on current programs to identify inefficiencies, and ensuring manufacturing processes meet quality standards. The Quality Engineer will also lead PFMEA audits and work closely with the manufacturing team.</p><p><br></p><h2>Responsibilities</h2><ul><li>Lead and manage multiple PPAP submissions, ensuring timely and accurate delivery using customer-specific formats.</li><li>Participate in APQP meetings and support the development of quality processes, including PFMEAs, Control Plans, and inspection documentation.</li><li>Develop and maintain PFMEAs and Control Plans, and lead PFMEA audits to ensure process robustness.</li><li>Run 8D problem-solving processes on current programs to identify root causes, inefficiencies, and implement corrective actions.</li><li>Submit and present PPAP packages for customer review, driving completion to meet deadlines and documentation requirements.</li><li>Support quality technicians on the floor, answering technical questions related to blueprints.</li><li>Analyze inspection data using Excel to evaluate dimensional results and make recommendations to customers based on findings.</li><li>Interface directly with customers, providing updates, addressing concerns, and ensuring satisfaction with quality deliverables.</li><li>Collaborate with press operators and manufacturing teams to resolve quality issues and improve part production processes.</li><li>Monitor tool and shift transitions to ensure adherence to quality processes and prevent defects.</li><li>Manage engineering changes, ensuring proper documentation, communication, and implementation across teams.</li><li>Organize and input customer data into internal systems, updating work instructions and maintaining accurate quality records.</li><li>Track and manage over 20 open quality projects, ensuring progress, accountability, and timely resolution.</li></ul><h2>Essential Skills</h2><ul><li>At least 5 years of experience in Quality Engineering.</li><li>Proficiency in IATF standards.</li><li>Experience with PPAP - ability to write, review, and submit to customers.</li><li>Experience in high volume manufacturing in plastics or metals.</li><li>ERP experience, preferably with Plex.</li><li>Program management skills.</li><li>Experience with metal stamping </li></ul><h2>Work Environment</h2><p>This is an on-site role with working hours from 8 AM to 5 PM. </p><p>The position involves both office and floor work. The company comprises 85 employees, with a dedicated quality team of 5 members. </p><p>The role offers growth opportunities, especially for those who have led teams without holding a managerial title. </p>

<h1 style="font-weight: 700;">Job Title: Quality Engineer</h1><br><h2>Job Description</h2><p>We are seeking a dedicated Quality Engineer to drive continuous improvement activities and enhance manufacturing processes. The role involves ensuring that manufacturing processes meet engineering requirements through capability studies and gauge R&amp;R analysis. You will be instrumental in resolving quality issues using quality tools and continuous improvement methods.</p><br><h2>Responsibilities</h2><ul><li>Provide daily support to manufacturing value streams, including audits and analysis to maintain quality standards.</li><li>Coordinate supplier corrective actions, document supplier issues, and work with procurement engineers to resolve problems.</li><li>Support new product introduction and implementation.</li><li>Conduct capability studies and gauge R&amp;R analysis to ensure manufacturing processes meet engineering requirements.</li></ul><h2>Essential Skills</h2><ul><li>Quality engineering</li><li>PPAP (Production Part Approval Process)</li><li>Root cause analysis</li><li>Quality management</li><li>APQP (Advanced Product Quality Planning)</li><li>Corrective action plans</li><li>Lean manufacturing</li><li>Problem-solving methods</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s Degree within Engineering field preferred</li><li>Blueprint reading and GDT (Geometric Dimensioning and Tolerancing) experience</li><li>Assembly and manufacturing process knowledge</li><li>Supplier quality management</li></ul><h2>Work Environment</h2><p>You will be working in a manufacturing facility that produces forklifts and distributes globally. The facility operates continuous manufacturing as well as custom project-based work. Candidates will work a Monday to Thursday work week with occasional overtime on Friday and remote work as needed. The environment is typical for manufacturing, being cold in the winter and hot in the summer. Enjoy a clean facility where you can work on interesting projects and custom orders. The position is first shift with the benefit of a 4-day work schedule, allowing for a great work-life balance.</p><br>

<h1><strong>Job Title: Quality Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>The Quality Engineer will play a critical role in overseeing product launches and the daily management of processes, products, and equipment. This position involves comprehensive involvement from initial stages to completion, including supplier quality, internal quality, process development, and documentation changes that support manufacturing, quality audits, and preparation for third-party audits.</p><p><br></p><h2>Responsibilities</h2><ul><li>Develop and implement all quality-related processes and documentation for new program development and current sustainment business.</li><li>Engage directly in manufacturing process development and continuous improvement to meet or exceed quality metrics and process metrics for current and new business.</li><li>Review, analyze, and resolve customer, internal, and supplier quality issues through root cause analysis and implementation of corrective actions.</li><li>Develop and implement preventative actions and continuous improvements within manufacturing and quality areas.</li><li>Control the non-conformance area including inventory, disposition, and associated costs.</li><li>Manage and review gage equipment, certifications, and calibrations, including programming CMM or other coordinate measurement equipment.</li><li>Ensure the calibration log is complete and up-to-date.</li><li>Coordinate with the quality inspector for daily inspection, measurement, testing, and approval of all components, products, and processes using quality metrics to ensure targets are met.</li><li>Communicate and coordinate with management, administrative, operations, quality, and engineering departments.</li><li>Utilize quality management system software and SPC systems daily.</li><li>Participate in conducting supplier and internal system and process audits.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor&#39;s Degree in Engineering.</li><li>3+ years&#39; experience working in quality within medical device industry (can be OEM or contract manufacturer).</li><li>Experience working with ISO13485 standards.</li><li>Process capability experience related to processes, production, equipment, and assembly.</li><li>Product development experience.</li><li>Strong problem-solving methodology, including systematic approaches like 5Y, Fishbone, and 8D.</li><li>Proficiency in quality statistics, metrology, biomedical technologies, auditing, Six Sigma, machining, fabrication, and assembly.</li></ul><h2>Work Environment</h2><p>The facility is located in Kalamazoo and operates as a satellite operation with a total of 50-60 employees. The Quality Team comprises 2 quality technicians and quality inspectors, along with 2 Quality Engineers. Minimal travel is required, up to 5% within the US and Canada. Work hours range from 40-45 hours per week. This position offers 10 days of PTO and 6 standard holidays.</p>

<h1 style="font-weight: 700;">Job Title: Quality Engineer</h1><br><h2>Job Description</h2><p>Join a medium-sized supplier experiencing international growth as a Quality Engineer specializing in acoustical, thermal, and electromagnetic insulation for passenger cars and commercial vehicles. You will be part of a team using six production technologies: Thermoforming, Aluminumforming, PU Foaming, Die Cutting, Vacuumforming, and Blow Moulding. This role offers the opportunity to advance to Quality Manager within a year.</p><br><h2>Responsibilities</h2><ul><li>Create Production Part Approval Processes (PPAPS) and engage in Advanced Product Quality Planning (APQP).</li><li>Utilize the ERP system, specifically SAP.</li><li>Collaborate with a quality inspector to ensure product quality standards are met.</li></ul><h2>Essential Skills</h2><ul><li>A minimum of 3 years of quality experience in an automotive setting.</li><li>Experience with IATF audits.</li><li>Participation in PPAP/APQP processes.</li><li>A relevant degree.</li><li>Proficiency in SAP.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Familiarity with SAP.</li></ul><h2>Work Environment</h2><p>Enjoy a 40-hour workweek from 8 AM to 5 PM, Monday through Friday, working closely with a quality inspector. Benefit from access to Udemy after six months, enhancing your automotive industry experience.</p><br>

<h1 style="text-align: center;"><strong>Hiring for a Quality Engineer in Shelton, CT!</strong></h1><p><br></p><h2>Job Description</h2><p>As a Quality Engineer, you will ensure the correct application of advanced quality planning and engineering practices to enhance the quality, reliability, and acceptance of systems, processes, and products. You will provide a high level of quality customer service to both internal and external customers and suppliers.</p><p><br></p><h2>Responsibilities</h2><ul><li>Monitor the performance of product quality and reliability systems.</li><li>Assist and coordinate Automotive Industry Action Group (AIAG) disciplines, including APQP, PCP, PFMEA, PFC, SPC, MSA/GR&amp;R, Metrology Inspection Methods, PPAP, and Problem Solving using the 8-D and 3 Why methodology.</li><li>Generate and maintain accurate documentation related to quality, reliability, and processes.</li><li>Implement prevention/detection systems to eliminate problems affecting quality and reliability.</li><li>Prepare and present PPM reports, cost of quality reports, and other metrics.</li><li>Develop and implement quality programs, including tracking, analyzing, reporting, and problem solving.</li><li>Accurately file all quality paperwork, including customer complaints, control plans, quality alerts, and weekly logs.</li><li>Participate in pre-production activities as a quality representative.</li><li>Complete quality system audits of suppliers on-site and follow up on corrective actions.</li><li>Issue supplier non-conformance reports and follow up on problem solving with suppliers.</li></ul><h2>Essential Skills</h2><ul><li>BS in Engineering or other technical discipline.</li><li>Minimum 8 years of experience in a Quality Department within a manufacturing environment.</li><li>Proficiency in blueprint reading and GD&amp;T interpretation.</li><li>Knowledge and experience with ISO9001 and IATF16949 documentation systems.</li><li>Basic understanding of performing dimensional inspections using standard metrology equipment.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>ASQ Certified Quality Engineer (CQE) preferred.</li><li>Experience in the automotive industry preferred.</li><li>Proficiency in AIAG disciplines.</li><li>Experience with CMMs, Keyence Vision Systems, or similar systems is advantageous but not required.</li></ul><h2>Work Environment</h2><p>The work environment involves working within a manufacturing setting, where you will use various technological tools and equipment. The role may require occasional travel and adherence to safety expectations and company policies. Regular and punctual attendance is expected, along with maintaining a clean and organized workspace.</p>

<h1><strong>Job Title: Quality Engineer</strong></h1><p><strong><em><u>For immediate consideration, please email your resume and interview availability to (sanmalik@actalentservices.com) ASAP today or tomorrow. I am conducting interviews this week and looking to hire immediately.</u></em></strong></p><h2>Job Description</h2><p>Ensure the correct use of advanced quality planning and engineering to enhance quality, reliability, and acceptance of systems, processes, and products. Provide a professional level of quality customer service to both internal and external customers and suppliers.</p><p><br></p><h2>Responsibilities</h2><ul><li>Monitor the performance of product quality and reliability systems.</li><li>Assist and coordinate Automotive Industry Action Group (AIAG) disciplines such as Advanced Product Quality Planning (APQP), Process Control Plan (PCP), Process Failure Mode &amp; Effect Analysis (PFMEA), Process Flow Chart (PFC), Statistical Process Control (SPC), Measurement System Analysis (MSA) / Gage Repeatability &amp; Reproducibility (GR&amp;R), Metrology Inspection Methods and Strategies, Production Part Approval Process (PPAP), and Problem Solving using the 8-D and 3 Why methodology.</li><li>Generate and maintain accurate documentation relating to quality, reliability, and process.</li><li>Implement prevention/detection systems to eliminate problems affecting quality and reliability.</li><li>Prepare and present PPM (parts per million) reports, cost of quality reports, and other metrics reports.</li><li>Develop and implement quality programs, including tracking, analyzing, reporting, and problem-solving.</li><li>File all Quality paperwork accurately, including customer complaints, control plans, quality alerts, and weekly logs.</li><li>Take an active part in training and helping others as required and participate in continuous improvement teams.</li><li>Participate in pre-production activities as a quality representative.</li><li>Complete Quality System audits of supplier on-site, follow-up audit, and corrective action.</li><li>Issue supplier non-conformance and follow-up corrective action, and problem-solving with suppliers.</li><li>Coordinate Management Review process.</li><li>Assist in supplier evaluations for on-site audits.</li><li>Provide support for Quality Assurance Manager.</li><li>Use a computer to accurately enter all company-required information for data collection.</li><li>Safely operate all required lifting/moving devices.</li><li>Attend all company-specified training as required.</li><li>Participate in continual improvement.</li><li>Maintain a clean and organized work area.</li><li>Comply with Safety Expectations.</li><li>Ensure regular and punctual attendance at work.</li><li>Comply with relevant policies, procedures, and instructions, including Code of Conduct.</li><li>Occasional travel may be required.</li></ul><h2>Essential Skills</h2><ul><li>Quality engineering expertise.</li><li>Proficiency in blueprint reading and GD&amp;T interpretation.</li><li>Experience with ISO 9001 and IATF16949 documentation systems.</li><li>ASQ or CQE certification.</li><li>AIAG Disciplines proficiency.</li><li>BS in Engineering or other technical discipline.</li><li>Minimum 8 years of experience in a Quality Department within a manufacturing environment.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>ASQ Certified Quality Engineer (CQE) preferred.</li><li>Experience in the automotive industry is preferred.</li><li>Basic understanding of performing dimensional inspections of metallic components using standard metrology equipment such as calipers, micrometers, pin gages, height gages, and indicators.</li><li>Experience with CMMs, Keyence Vision Systems, or similar equipment is preferred.</li></ul><h2>Work Environment</h2><p>This role may require occasional travel and involves working in a manufacturing environment. The position demands regular and punctual attendance, adherence to safety expectations, and compliance with company policies and procedures. The work area should be maintained clean and organized at all times.</p>

<h1><strong>Job Title: Quality Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>This manufacturing facility is undergoing an expansion to develop new products by summer. We are seeking a Quality Assurance Engineer to assist in the creation and standardization of inspection and quality processes. The ideal candidate will understand how to read mechanical drawings to identify inspection points within them. They will take these inspection points and establish a process for quality technicians to verify and validate them. Additionally, they will create an SOP for the respective inspection points and select the appropriate tooling and gauges to ensure conformance.</p><p><br></p><h2>Responsibilities</h2><ul><li>Read and interpret mechanical drawings to identify inspection points.</li><li>Develop processes for quality technicians to verify and validate inspection points.</li><li>Create SOPs for inspection points and select suitable tooling and gauges.</li><li>Conduct non-conformance checks when inspection points are off value.</li><li>Create non-conformance SOPs to identify root causes and corrective actions.</li></ul><h2>Qualifications</h2><ul><li>Quality control experience</li><li>Ability to interpret and understand mechanical drawings</li><li>Strong production experience</li><li>Root cause analysis</li><li>Mechanical design</li><li>Proficiency in Microsoft Suite</li><li>Test build experience</li><li>3+ years of experience in quality control</li><li>Knowledge of calibration, gauges, and tooling equipment</li></ul><h2>Work Environment</h2><p>The role requires working within a high-pressure environment, primarily in an office setting with occasional time on the production floor. This position is on-site, five days a week, during the first shift. Although this is a contract role, there is potential for it to transition into a full-time position. The facility expansion provides ample engineering opportunities and growth within the company.</p>

<h1><strong>Job Title: Quality Engineer</strong></h1><p><strong><em>For immediate consideration, please apply directly to this job posting AND email me at habels @actalentservices.comwith the following:</em></strong></p><p><strong>1) Word copy of resume</strong></p><p><strong>2) 2-3 professional references</strong></p><p><strong>3) 4-5 brief bullet points highlighting technical qualifications</strong></p><p><br></p><h2>Job Description</h2><p>As a Quality Engineer, you will assist in the development of departmental processes, document control, and goals with compliance to AS9100D, focusing on continuous improvement initiatives and the implementation of process improvements throughout the organization. You will be responsible for ensuring manufacturing adherence to procedures and developing inspection documentation for receiving, in-process, and final inspection. Additionally, you will assist in reviewing internal and external non-conformances and coordinating corrective action responses to prevent recurrence. Your role will also include monitoring supplier performance and coordinating government inspections. You will provide quality interface and expertise within the business unit, establish and maintain quality management systems (ISO-9001 and AS9100D), and ensure customer satisfaction through quality.</p><p><br></p><h2>Responsibilities</h2><ul><li>Assist in the development of departmental processes, document control, and goals with compliance to AS9100D.</li><li>Focus on continuous improvement initiatives and implement process improvements throughout the organization.</li><li>Ensure manufacturing adherence to procedures and develop inspection documentation for receiving, in-process, and final inspection.</li><li>Review internal and external non-conformances and coordinate corrective action responses to prevent recurrence.</li><li>Monitor supplier performance and coordinate government inspections.</li><li>Provide quality interface and expertise within the business unit.</li><li>Establish and maintain quality management systems (ISO-9001 and AS9100D).</li><li>Support current business operations, including manufacturing support, inspection and test, supplier monitoring, and customer support.</li></ul><h2>Essential Skills</h2><ul><li>Formal technical/engineering degree (BSME or equivalent) with at least 8+ years of experience.</li><li>Proficiency with Quality Engineering principles such as 5 Whys, Fishbone, and statistical process controls.</li><li>Experience applying quality engineering principles to low volume/high mix manufacturing for complex Defense/Military projects.</li><li>Experience with Quality Management Systems (QMS), Audits, NCRs, MRB, and project management.</li><li>Knowledge of AS9100 and ISO9001 standards.</li><li>Ability to manage projects for defense and government-related projects.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with aerospace and defense projects.</li><li>Experience working for major defense contractors like Raytheon, Boeing, Lockheed, and Northrop.</li><li>Familiarity with metrology equipment, calibration equipment, GD&amp;T, and machining.</li><li>Project management skills and experience with work instruction, CNC machining, welding, and job costing software.</li></ul><h2>Work Environment</h2><p>Join a leading provider of cutting-edge aerospace and military technologies, where excellence and innovation are key. Work in a fast-paced, collaborative environment free of politics. The company is growing rapidly, offering diverse projects and opportunities for career advancement. There is exposure to facility expansion, plant layout, equipment layout, and transfer projects into new spaces. The culture is highly collaborative, emphasizing teamwork and professional growth.</p>

<h1><strong>Job Title: Quality Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a Quality Engineer with a <span style="color: rgb(8, 7, 7); background-color: none;">background</span> in design transfer and sustaining engineering to support the launch and scale-up of a new medical device. This role requires close collaboration with Manufacturing Engineering to ensure a seamless transition from design to production, emphasizing quality systems, risk management, and regulatory compliance.</p><p><br></p><h2>Responsibilities</h2><ul><li>Work closely with the manufacturing engineer to ensure the client&#39;s design is accurately translated onto the manufacturing line.</li><li>Conduct risk assessments and execute FMEA testing.</li><li>Perform sterilization (Gamma type) on products.</li><li>Create and manage Bill of Materials (BOM).</li><li>Verify that equipment or systems are installed correctly and according to manufacturer specifications (IQ).</li><li>Confirm that the equipment or system operates as intended across all specified operating ranges (OQ).</li><li>Demonstrate that the entire process, using the qualified equipment, consistently produces acceptable products under real-world conditions (PQ).</li></ul><h2>Essential Skills</h2><ul><li>Proven experience in design transfer.</li><li>Experience with risk assessments and FMEA testing.</li><li>Knowledge of quality management systems (QMS).</li><li>Proficiency in IQ, OQ, PQ processes.</li><li>Experience working with metal and steel hardware.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with orthopedic companies or surgical robotic companies.</li><li>Familiarity with sterilization processes, specifically Gamma type.</li></ul><h2>Work Environment</h2><p>Located in Fremont, CA, this position offers the opportunity to work at two distinct sites: a contract manufacturing plant and a design and development lab. The design and development site is currently expanding and gaining more NPI projects, providing exposure to innovative products in pre-commercialization as well as overseeing sustaining projects post-commercialization.</p>

<h1><strong>Job Title: Quality Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a skilled and experienced Quality Engineer with experience in aerospace or automotive industries to join our dynamic team. The role will focus primarily on interpreting customer and regulatory requirements, creating internal documentation, and ensuring these requirements are effectively implemented. This position offers the opportunity to contribute significantly to our projects with leading industry partners.</p><p><br></p><h2>Responsibilities</h2><ul><li>Facilitate First Article Inspection creation and submission.</li><li>Develop, maintain, and enhance quality data collection, analysis, and reporting systems.</li><li>Lead the implementation of Quality Management System enhancements, ensuring compliance with industry and customer standards.</li><li>Oversee quality guidelines, controls, and inspection procedures throughout product development and production stages.</li><li>Manage supplier qualification and auditing processes.</li><li>Support product development with risk analysis, FMEA/PFMEA, and reliability assessments.</li><li>Guide teams through root cause analysis and problem-solving using Six Sigma, lean methodologies, and statistical tools.</li><li>Oversee metrology and calibration programs to ensure proper measurement and conformity standards.</li><li>Plan and execute employee training, development, and succession planning initiatives.</li><li>Ensure adherence to plant safety rules and protocols.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in root cause analysis and quality engineering.</li><li>Experience with ISO 9001 and AS9100 standards.</li><li>Strong skills in PPAP/APQP, corrective action plans, and quality management systems.</li><li>Capability in inspection, PFMEA, and statistical process control.</li><li>Knowledge of lean methodology and Six Sigma principles.</li><li>Associates Degree within an Engineering Discipline.</li><li>Minimum of 3 years of experience as a Quality Engineer within heavy metal machinery manufacturing (preference for aerospace or automotive industries).</li><li>Minimum of 3 years of experience in First Article Inspection creation and submission.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Military experience is advantageous.</li><li>AS13000 Standards Certification is preferred.</li><li>Six Sigma Certification is a plus.</li></ul><h2>Work Environment</h2><p>The work environment is a climate-controlled facility, despite the shop being somewhat dirty. With over 100 CNC machines, this role operates on the first shift from Monday to Friday, starting at 7:00 AM ET and typically ending around 4:00 PM ET. Expect a 40-45 hour work week with minimal day trip traveling to customers.</p>

<h1 style="font-weight: 700;">Job Title: Quality Engineer - NPI</h1><br><h2>Job Description</h2><p>In this role, you will lead the design for manufacture and assembly by providing technical leadership and guidance in quality assurance, quality control, and preventative activities. You will support the development and introduction of new products, processes, and technologies with a focus on quality systems development, regulatory compliance, and process risk management. Your role involves developing and characterizing processes that are capable, scalable, and produce high yield, while also designing robust inspection strategies.</p><br><h2>Responsibilities</h2><ul><li>Foster collaborative internal and external professional relationships across design divisions and functions related to design transfer activities.</li><li>Communicate effectively with internal customers, stakeholders, and project teams to ensure successful project transfers.</li><li>Mentor other groups on design and process transfer expertise.</li><li>Develop and implement methods for process control and improvement to ensure product quality.</li><li>Collaborate with suppliers to address quality issues and contribute to supplier quality improvement programs.</li><li>Manage risk by employing risk management practices and tools, with a focus on failure modes and process controls.</li><li>Ensure compliance with ISO14971 standards and support the design team in risk identification and mitigation.</li><li>Develop and implement lean inspection strategies and lead continuous improvements in inspection methods.</li><li>Lead and approve validation strategies and influence processes towards validation.</li><li>Apply statistical techniques to develop robust quality systems and provide expertise for non-conformances and corrective actions.</li><li>Lead supplier qualification strategies and support the implementation of supplier certification.</li><li>Represent quality assurance in design transfer processes and ensure product launches meet established targets.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in risk management and PFMEA</li><li>Experience with validation and quality engineering in medical devices</li><li>Knowledge of ISO14971 and design transfer processes</li><li>Bachelor of Science in Engineering or related field with 3-5 years of experience in a quality or technical discipline</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in developing inspection strategies and using measurement system analysis (MSA)</li><li>Knowledge in CQA and CTQ processes</li><li>Ability to overhaul production processes and align procedures</li></ul><h2>Work Environment</h2><p>This position requires working onsite. The role is an individual contributor position that requires independent work with minimal supervision. Standard benefits are offered, including 2 weeks of PTO and 10 paid holidays.</p><br>

Quality Engineer - NPI / P

<h1 style="font-weight: 700;">Job Title: Quality Engineer/CMM Programmer</h1><br><h2>Job Description</h2><p>In this role, you will function as a Quality Engineer, supporting the quality manager by utilizing your skills with micrometers and calipers while working with metals. You will engage in hands-on activities both in the lab and on the production floor, collaborating alongside CNC machines. Daily communication with suppliers about orders will be a key responsibility.</p><br><h2>Responsibilities</h2><ul><li>Support the quality manager in maintaining high-quality standards.</li><li>Utilize micrometers and calipers for precise measurements.</li><li>Work in both lab and production floor environments.</li><li>Collaborate closely with CNC machines.</li><li>Communicate daily with suppliers regarding orders.</li><li>Ensure responsibility for the first piece process.</li><li>Operate and program CMM equipment.</li></ul><h2>Essential Skills</h2><ul><li>Proficient in using micrometers and calipers.</li><li>Experience with castings and forgings in the industry for at least 6 months.</li><li>Minimum of 2 years of experience as a Quality Engineer.</li><li>At least 2 years of experience in CMM operating or programming.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Knowledge of GD&amp;T and PPAP processes.</li><li>Familiarity with IATF standards.</li><li>Blueprint reading and interpretation skills.</li></ul><h2>Work Environment</h2><p>The work environment consists of a team of 50 employees. You will be greeted by Snickers, a friendly dog at the front, emphasizing a welcoming and inclusive atmosphere.</p><br>

Quality Engineer/CMM Programmer

<h1><strong>Job Title: Quality Engineering Technician</strong></h1><p><br></p><h2>Job Description</h2><p>The primary objective of this role is to ensure quality in manufacturing and supply chain in support of the development and production of the driver, delivering the benefits of self-driving technology safely, quickly, and broadly. A successful candidate understands quality processes, possesses strong attention to detail, has a quality-focused mindset, and can contribute to cross-functional teams to identify and eliminate quality problems, issues, and risks.</p><p><br></p><h2>Responsibilities</h2><ul><li>Lead and support inspection and test plan creation in coordination with engineering.</li><li>Provide guidance related to part inspection and test procedures.</li><li>Perform inspections (first article, incoming, in-process, outgoing) according to inspection plans and procedures to record, analyze data, document, and report results.</li><li>Perform tests (qualification, incoming, in-process, end-of-line) according to test plans and procedures to record, analyze data, document, and report results.</li><li>Conduct physical inspections using various gauges, tools, and inspection equipment.</li><li>Perform dimensional and gauge studies (MSA, R&amp;R) in coordination with engineering.</li><li>Carry out cable and harness assembly testing and troubleshooting.</li><li>Perform soldering and wire splicing inspections.</li><li>Assemble electromechanical modules.</li><li>Execute inventory physical and electronic transactions as needed.</li><li>Operate inspection and test fixtures or equipment, with the ability to train others as required.</li><li>Assist in training manufacturing teams and technicians on in-process inspections and/or tests.</li><li>Support activities related to non-conforming product(s) and returned material authorization activities (Material Review Board).</li><li>Participate in layered audit and manufacturing process audit activities.</li><li>Actively engage in continuous improvement activities.</li><li>Follow and support company safety requirements, policies, procedures, and work instructions.</li><li>Adhere to written, verbal, and visual instructions.</li><li>Perform other duties as assigned.</li></ul><h2>Essential Skills</h2><ul><li>Quality assurance expertise in automotive manufacturing and electro-mechanical assembly operations.</li><li>3+ years of experience in quality automotive manufacturing, robotics, or equivalent field.</li><li>Proficiency in debugging complex electronic assemblies and manufacturing cable assemblies.</li><li>Experience with CNC mills, lathes, and other machine shop tools.</li><li>Understanding of electrical and mechanical drawings.</li><li>Proficient in using various gauges, measuring devices, and equipment.</li><li>Experience with Linux operating systems.</li><li>Experience with Google Sheets, Docs, Slides, and Gmail.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>An Associate Degree, Technician Certificate, or equivalent in engineering/photonics/lasers/electro-optics.</li><li>IPC 610 and IPC 620 certifications.</li><li>Attention to detail and careful handling of precision components and equipment.</li></ul><h2>Work Environment</h2><p>This is an on-site position with meals provided.</p>

Quality Engineering Technician

<h1 style="font-weight: 700;">Job Title: Quality Environmental Monitoring Specialist</h1><br><h2>Job Description</h2><p>The Quality Environmental Monitoring Specialist will work on the 1st shift to conduct environmental monitoring and sampling within cleanrooms and controlled areas. The role involves maintaining accurate documentation and adhering to quality procedures to ensure cleanliness and compliance.</p><br><h2>Responsibilities</h2><ul><li>Perform environmental monitoring of cleanrooms and controlled areas, including viable air, non-viable particles, critical surface monitoring, and personnel monitoring.</li><li>Collect routine environmental samples from surfaces, air, and water.</li><li>Maintain accurate and complete documentation of sampling information and results in compliance with Good Documentation Practices (GDP).</li><li>Label environmental samples appropriately and submit them to the laboratory via LIMS.</li><li>Submit finished good products for additional testing.</li><li>Review and perform trending on environmental monitoring results.</li><li>Assist with investigations related to out-of-specification (OOS) results, excursions, or contamination events.</li><li>Adhere to internal quality procedures, specifically related to proper gowning, hygiene, and microbial control, to maintain cleanliness within cleanrooms.</li><li>Assist in the development and implementation of processes, reports, data analysis, and procedures within the defined area of specialization.</li><li>Perform audits to review all related documentation for completeness, accuracy, and ensure the product and reports meet all specifications.</li></ul><h2>Essential Skills</h2><ul><li>Laboratory experience with emphasis on biology and microbiology.</li><li>Proficiency in aseptic techniques and GMP practices.</li><li>Strong documentation skills and experience with environmental monitoring and sampling.</li><li>Familiarity with LIMS, SOPs, and labeling practices.</li><li>Experience in quality control and cleanroom environments.</li><li>Ability to conduct investigations, handle deviations, and implement CAPA procedures.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High school graduate or GED required.</li><li>Associate or bachelor’s degree in biology, microbiology, or a science-related field preferred.</li><li>0 to 2 years of work experience within a manufacturing environment, with GMP experience preferred.</li><li>Attention to detail in sampling techniques and previous experience with environmental monitoring and aseptic technique preferred.</li><li>Strong time management, communication, and critical thinking skills.</li><li>Familiarity with LIMS or submission of samples to a laboratory.</li><li>Experience working with aseptic technique within an FDA-regulated environment.</li><li>Past participation in regulatory audits (FDA, ISO, etc.).</li></ul><h2>Work Environment</h2><p>The role operates during the 1st shift from 8:00 am to 4:30 pm. The Quality Assurance team consists of seven members, including six QA Engineers. The specialist will also interact with a team of 9-10 people in Quality Control, who conduct in-process testing and visual inspection. The Readycare division focuses on wipes for cosmetic and pharmaceutical industries, serving long-term care facilities, hospitals, and retail spaces.</p><br>

Quality Environmental Monitoring Specialist

<h1 style="text-align: center;"><strong>Quality Field Technician</strong></h1><p><br></p><h2>Job Description</h2><p>The Quality Field Technician plays a crucial role in ensuring the satisfaction of customers, team members, and vendors by managing quality-related duties. This position involves providing on-shift coordination and support for quality issues on the manufacturing production floor, while developing and maintaining basic quality systems related to manufacturing high-quality products. The technician will perform analytical testing and determine product conformance to specifications in real-time, following Good Manufacturing Practices, particularly in the manufacture of extended shelf life (ESL) dairy products.</p><p><br></p><h2>Responsibilities</h2><ul><li>Achieve assigned goals in production, safety, quality, performance, and cost.</li><li>Notify others of mechanical malfunctions to enhance productivity and equipment capabilities; identify areas where operators can assist in resolving concerns.</li><li>Comply with GMPs, SOPs, corporate and plant policies, rules, and regulations.</li><li>Provide assistance and support to all areas related to quality as assigned by supervisor/lead.</li><li>Maintain focus on all quality checks performed by technicians; provide follow-up training as needed.</li><li>Perform finished pallet audits, end-of-shift product reviews, and other quality checks to ensure standards are met.</li><li>Track packaging/processing Key Quality Attributes (KQAs) and identify problem areas and trends.</li><li>Respond to production operator’s quality questions and concerns.</li><li>Communicate effectively between shifts and other departments; execute issue resolution and escalate issues in a timely manner.</li><li>Communicate product disposition and assist Operations with compliance to standards.</li><li>Ensure inventory accuracy of product in Quality Hold/retest status; perform routine cycle counts and reconciliations.</li><li>Audit Operations paperwork for timely completion and accuracy.</li><li>Participate in Internal Quality Audit process to improve plant quality systems and GMP compliance.</li><li>Serve as a resource to Operations for auditing, updating, and documenting compliance to the Master Sanitation Schedule.</li><li>Conduct titration testing, verify chemical concentrations, and verify CIP dilution samples as needed.</li><li>Conduct troubleshooting as needed.</li><li>Perform finished product weight verifications and checks, including volumetric checks.</li><li>Complete sensory analysis on finished products as required.</li><li>Conduct investigative research on products or materials as assigned.</li><li>Conduct ATP cleaning verification and line release process per shift.</li><li>Perform Environmental Swabbing as requested by QA Management.</li><li>Set up documentation and complete sample shipments using proper shipping methods.</li><li>Cover breaks, lunches, and other staffing needs as assigned by supervisor/lead.</li><li>Comply with all legal requirements concerning dairy processing and safety; report concerns to supervisor/lead.</li><li>Work safely and report safety concerns promptly to supervisor/lead; take corrective actions to ensure a safe environment.</li><li>Report food safety problems and initiate action; support SQF by maintaining food safety and quality.</li><li>Ensure work areas are sanitary and adhere strictly to sanitation practices.</li></ul><h2>Essential Skills</h2><ul><li>Ability to apply basic to complex mathematical concepts, including adding, counting, subtracting, multiplying, dividing, and knowledge of weights and measures.</li><li>Basic statistics and statistical process control with attention to detail.</li><li>Ability to understand and respond appropriately to basic and complex inquiries from employees, vendors, and customers.</li><li>Proficiency in reading, writing, and communicating in English to perform job functions.</li><li>Knowledge of company&#39;s mission, purpose, goals, and the role in achieving each of them.</li><li>Ability to operate quality and facility equipment as required.</li><li>Completion of all company training requirements.</li><li>Ability to interpret company documents, literature, and UPC/code information.</li><li>Experience with Microsoft Windows and software architecture.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Minimum of GED or High School Diploma required; Associates degree in chemistry, biology, food science, or ag-tech science preferred.</li><li>6 months to 2 years of manufacturing/machine operation experience in the dairy/food industry preferred.</li><li>Experience with SQF or similar quality systems preferred.</li></ul><h2>Work Environment</h2><p>The work environment involves ensuring compliance with GMP dress code standards, maintaining a safe work environment, and adhering to sanitation practices. Employees must report to work at scheduled times, communicate tardiness and absences, and be well-groomed and dressed in business-appropriate attire. The role demands maintaining safety standards, promptly reporting and correcting safety concerns, and complying with performance criteria and company policies.</p>

Quality Field Technician

<h1><strong>Quality Hygienist</strong></h1><p><br></p><h2>Job Description</h2><p>As a Quality Hygienist, you will play a crucial role in protecting the safety and quality of our product. You will be responsible for maintaining pre-requisite components of the Food Safety Management System by establishing, maintaining, and coaching the building blocks of hygiene and food safety concepts in the manufacturing facility. Your expertise in hygiene and sanitation will be essential to maintaining the highest standards for our environment and products. You will also be responsible for identifying and addressing potential food safety risks and ensuring that our manufacturing processes adhere to best practices.</p><p><br></p><h2>Responsibilities</h2><ul><li>Define, implement, and verify the effectiveness of the Pre-requisite Programs (PRP&#39;s) related to Hygiene, including hygienic zoning, risk management, pest control, cleaning validation and verification, pathogen monitoring, foreign body prevention, hygiene, and housekeeping.</li><li>Contribute to skills development of quality and operations personnel across the organization.</li><li>Define and update the specific quality and sanitation standard operating procedures, instructions, and tools required to operate in a facility.</li><li>Support operations and maintenance in ensuring GMP standards are adhered to.</li><li>Support the new product or process development through the risk assessment of new raw materials and processes.</li><li>Develop audit routines to ensure the effectiveness of the sanitation program.</li><li>Support activities to achieve compliance with organizational requirements and other applicable instructions and standards.</li><li>Own and deliver training related to hygiene, sanitation, and housekeeping as required.</li><li>Lead and support the development and implementation of Sanitation Standard Operation Procedures.</li><li>Recommend improvements to the master cleaning and master sanitation registers.</li><li>Support facility readiness for internal and external audits.</li><li>Perform troubleshooting and corrective action follow-up of non-conformities.</li><li>Comprehend and support plant protocols and programs, as well as facility systems, including informational/operational/management systems such as Acadia and QMS.</li><li>Develop and execute the environmental monitoring program.</li><li>Support sample collection and analysis at specified stages in the production process for evaluating compliance to specification.</li><li>Perform maintenance hygiene verification inspections.</li><li>Conduct CIP verification, pre-operational inspections, and collect pre-op cleaning verification swabs, reporting any concerns or deviations.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in microbiology, biology, chemistry or a comparable program, or an equivalent combination of education and experience.</li><li>Experience successfully implementing sanitation, quality, or food safety programs by leading change or participating in project teams or improvement projects.</li><li>Demonstrated competence in hygiene and quality management.</li><li>Experience working in a microbiology or quality role in a food manufacturing environment.</li><li>Excellent verbal and written communication skills.</li><li>Proficiency in MS Office.</li><li>Strong writing, analytical, presentation, and critical thinking skills.</li><li>Detail-oriented and possesses strong decision-making ability.</li><li>Ability to keep accurate records.</li></ul>

Quality Hygenist

<h1><strong>Job Title: Quality Hygienist</strong></h1><p><br></p><h2>Job Description</h2><p>As a Quality Hygienist, you will play a crucial role in protecting the safety and quality of our product. You will be responsible for maintaining the pre-requisite components of the Food Safety Management System by establishing, maintaining, and coaching the building blocks of hygiene and food safety concepts in the manufacturing facility. Your expertise in hygiene and sanitation will be essential to maintaining the highest standards for our environment and products. You will also be responsible for identifying and addressing potential food safety risks and ensuring that our manufacturing processes adhere to best practices. This role will report to the Food Safety and QA Manager.</p><p><br></p><h2>Responsibilities</h2><ul><li>Define, implement, and verify the effectiveness of the Pre-requisite Programs (PRP&#39;s) related to hygiene, including hygienic zoning, risk management, pest control, cleaning validation and verification, pathogen monitoring, foreign body prevention, hygiene, and housekeeping.</li><li>Contribute to the skills development of quality and operations personnel across the organization.</li><li>Define and update the specific quality and sanitation standard operating procedures, instructions, and tools required to operate in a facility.</li><li>Support operations and maintenance in ensuring GMP standards are adhered to.</li><li>Support new product or process development through the risk assessment of new raw materials and processes.</li><li>Develop audit routines to ensure the effectiveness of the sanitation program.</li><li>Support activities to achieve compliance with organizational requirements and other applicable instructions and standards.</li><li>Own and deliver training related to hygiene, sanitation, and housekeeping as required.</li><li>Lead and support the development and implementation of Sanitation Standard Operation Procedures.</li><li>Recommend improvements to the master cleaning and master sanitation registers.</li><li>Support facility readiness for internal and external audits.</li><li>Perform troubleshooting and corrective action follow-up of non-conformities.</li><li>Comprehend and support plant protocols and programs, as well as facility systems, including informational, operational, and management systems such as Acadia and QMS.</li><li>Responsible for development and execution of the environmental monitoring program.</li><li>Support sample collection and analysis at specified stages in the production process for evaluating compliance to specification.</li><li>Perform maintenance hygiene verification inspections.</li><li>Responsible for CIP verification, pre-operational inspections, collecting pre-op cleaning verification swabs, and reporting any concerns or deviations.</li></ul><h2>Essential Skills</h2><ul><li>Experience in successfully implementing sanitation, quality, or food safety programs by leading change or participating in project teams or improvement projects.</li><li>Competence in hygiene and quality management.</li><li>Experience working in a microbiology or quality role in a food manufacturing environment.</li><li>Excellent verbal and written communication skills.</li><li>Proficiency in MS Office.</li><li>Strong writing, analytical, presentation, and critical thinking skills.</li><li>Detail-oriented and strong decision-making ability.</li><li>Ability to keep accurate records.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in microbiology, biology, chemistry, or a comparable program, or an equivalent combination of education and experience.</li></ul><h2>Work Environment</h2><p>The role is based in a manufacturing environment.</p>

Quality Hygienist

<h1 style="font-weight: 700;">Job Title: Quality Inspector</h1><br><h2>Job Description</h2><p>The Quality Inspector is responsible for verifying and approving production runs, completing associated paperwork, and performing regular quality checks on products across various production machines. This role ensures products meet specifications and are ready for release for sale. The inspector follows all safety rules and company-established manufacturing and quality methods and processes while meeting Key Performance Indicators (KPIs). Responsibilities also include reading computer specifications, verifying lot numbers, quarantining products, and conducting root cause analysis. Quality checks are performed every 60 minutes on the production floor.</p><br><h2>Responsibilities</h2><ul><li>Verify and approve production runs.</li><li>Complete associated paperwork accurately.</li><li>Perform regular quality checks on production machines.</li><li>Ensure products meet specifications and are ready for sale.</li><li>Follow safety rules and company-established quality methods.</li><li>Meet Key Performance Indicators (KPIs).</li><li>Read computer specifications and verify lot numbers.</li><li>Quarantine products and conduct root cause analysis.</li><li>Perform 60-minute quality checks on the production floor.</li></ul><h2>Essential Skills</h2><ul><li>Quality Control</li><li>Quality Checks</li><li>Inspection</li><li>Documentation</li><li>FDA and/or GMP Experience</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>1+ years of experience in Quality Control or Inspection</li><li>Experience in GMP, though open to quality experience outside of that industry</li></ul><h2>Work Environment</h2><p>The position involves working both on the production floor to check products and in an office environment for documentation tasks. Employees enjoy a climate-controlled environment. The position will train on the first shift for 2-3 weeks before moving to the third shift. Shift hours are as follows: 1st shift: Monday to Friday, 6:00 AM – 2:30 PM; 2nd shift: Monday to Friday, 2:00 PM – 10:30 PM, with possible Saturday shifts every other week; 3rd shift: Sunday to Thursday, 10:00 PM – 6:30 AM. There is potential for overtime work, though it is not mandatory.</p><br>

Quality Inspector

<h1 style="font-weight: 700;">Job Title: Quality Inspector/Technician</h1><br><h2>Job Description</h2><p>This position involves a balanced mix of on-the-floor activities and documentation tasks. Key responsibilities include supporting non-conforming material processes, corrective actions, customer feedback records, calibration, internal audits, and work instructions. The role also involves using a network analyzer for electrical testing and product analysis, along with providing training to others.</p><br><h2>Responsibilities</h2><ul><li>Support non-conforming material processes and corrective actions.</li><li>Maintain customer feedback records and calibration documentation.</li><li>Conduct internal audits and manage work instructions.</li><li>Use a network analyzer for electrical testing and product analysis.</li><li>Train and mentor other team members.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency with micrometer, caliper, ruler, and blueprint reading.</li><li>Experience in quality inspection and final inspection processes.</li><li>Ability to conduct electrical inspections and testing.</li><li>Experience in electrical crimping and wiring.</li><li>Knowledge of GD&amp;T, CMM, VSWR, VOP, RF standards.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Minimum 2 years of experience in quality inspecting.</li><li>Minimum 2 years of experience with electrical properties such as VSWR, VOP, RF, and Ethernet cable.</li><li>Minimum 1 year of experience with AS9100 standards.</li><li>Minimum 2 years of experience with pin gauges, micrometers, and calipers.</li><li>Ability to read and interpret drawings and blueprints.</li></ul><h2>Work Environment</h2><p>The work environment is a very clean, air-conditioned production floor with a small shop and family feel, consisting of around 40 employees. The facility has recently moved to a new location near Majestic Theatre and offers a great culture that is inviting and collaborative. The department includes five individuals, fostering a close-knit team dynamic.</p><br>

Quality Inspector/Technician

<h1 style="font-weight: 700;">Job Title: Quality Lab Technician</h1><br><h2>Job Description</h2><p>The Lab Technician performs each essential duty safely, satisfactorily, and in a timely manner. This role involves understanding and following batch tickets with high accuracy, performing complex testing processes on production batches, and maintaining a clean and organized work environment.</p><br><h2>Responsibilities</h2><ul><li>Understand and follow a batch ticket (recipe) with high degree of accuracy for weights and measurements.</li><li>Perform a wide variety of complex testing processes on production batches to measure product’s physical or chemical characteristics, including viscosity, weight per unit of measure, flow, gloss, and color characteristics.</li><li>Test materials from suppliers and production batches.</li><li>Perform standard testing procedures, including preparation of materials with attention to detail and high quality.</li><li>Follow daily work plan for Lab Work Request or project plan.</li><li>Accurately document work in lab notebooks, whether physical or electronic.</li><li>Recognize roadblocks or anomalies and resolve them or communicate concerns with a chemist in a timely manner.</li><li>Ensure raw materials are available and correctly labeled.</li><li>Correctly label and mail samples.</li><li>Maintain a clean and organized work environment.</li><li>Tint batches without assistance.</li><li>Calculate resin composites.</li><li>Maintain QC records using a web-based computer system.</li><li>Prepare records for submission.</li><li>Perform tests using lab equipment such as viscosity, pH, weight per gallon, and % solids.</li><li>Conduct draw downs and use ovens.</li><li>Maintain and perform calibrations on machines.</li></ul><h2>Essential Skills</h2><ul><li>Chemistry</li><li>Laboratory skills</li><li>Color matching</li><li>Quality control</li><li>Lab Technician experience</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Not color blind</li><li>Prior quality/wet lab experience or entry-level graduate with AS or BS in Science</li><li>Prior experience with color matching is a plus</li><li>Experience working with paint, pigments, and coatings</li><li>Industrial lab experience doing basic wet chemistry, including viscosity, pH, and % solids</li></ul><h2>Work Environment</h2><p>This role is based in an industrial lab environment within the plant. Personal protective equipment (PPE) such as lab coats and safety glasses will be provided. On the first day of training, steel-toed boots/shoes will be required, and reimbursement will be provided. The facility may have strong smells of chemicals and paint, so applicants should not be sensitive to those. The lab is large, with at least five people on each shift at all times.</p><br>

Quality Lab Technician

<h1 style="text-align: center;"><strong><u>Quality Lab Technician</u></strong></h1><p style="text-align: center;"><br></p><p style="text-align: center;">INTERESTED CANDIDATES MAY SEND UPDATED RESUMES TO: JGASSER @ ACTALENTSERVICES.COM </p><p style="text-align: center;">OR TEXT JENNA TO SETUP A PHONE INTERVIEW: 419. 980. 5823</p><p><br></p><p><strong><u>Job Description</u></strong></p><p>The Lab Technician performs each essential duty safely, satisfactorily, and in a timely manner. This role involves understanding and following batch tickets with high accuracy, performing complex testing processes on production batches, and maintaining a clean and organized work environment.</p><p><br></p><p><strong><u>Responsibilities</u></strong></p><ul><li>Understand and follow a batch ticket (recipe) with high degree of accuracy for weights and measurements.</li><li>Perform a wide variety of complex testing processes on production batches to measure product’s physical or chemical characteristics, including viscosity, weight per unit of measure, flow, gloss, and color characteristics.</li><li>Test materials from suppliers and production batches.</li><li>Perform standard testing procedures, including preparation of materials with attention to detail and high quality.</li><li>Follow daily work plan for Lab Work Request or project plan.</li><li>Accurately document work in lab notebooks, whether physical or electronic.</li><li>Recognize roadblocks or anomalies and resolve them or communicate concerns with a chemist in a timely manner.</li><li>Ensure raw materials are available and correctly labeled.</li><li>Correctly label and mail samples.</li><li>Maintain a clean and organized work environment.</li><li>Tint batches without assistance.</li><li>Calculate resin composites.</li><li>Maintain QC records using a web-based computer system.</li><li>Prepare records for submission.</li><li>Perform tests using lab equipment such as viscosity, pH, weight per gallon, and % solids.</li><li>Conduct draw downs and use ovens.</li><li>Maintain and perform calibrations on machines.</li></ul><p><strong><u>Essential Skills</u></strong></p><ul><li>Chemistry</li><li>Laboratory skills</li><li>Color matching</li><li>Quality control</li><li>Lab Technician experience</li></ul><p><strong><u>Additional Skills &amp; Qualifications</u></strong></p><ul><li>Not color blind</li><li>Prior quality/wet lab experience or entry-level graduate with AS or BS in Science</li><li>Prior experience with color matching is a plus</li><li>Experience working with paint, pigments, and coatings</li><li>Industrial lab experience doing basic wet chemistry, including viscosity, pH, and % solids</li></ul><p><strong><u>Work Environment</u></strong></p><p>This role is based in an industrial lab environment within the plant. Personal protective equipment (PPE) such as lab coats and safety glasses will be provided. On the first day of training, steel-toed boots/shoes will be required, and reimbursement will be provided. The facility may have strong smells of chemicals and paint, so applicants should not be sensitive to those. The lab is large, with at least five people on each shift at all times.</p>

<h1 style="text-align: center;"><strong><u>Quality Lab Technician</u></strong></h1><p style="text-align: center;"><br></p><p style="text-align: center;">INTERESTED CANDIDATES MAY SEND UPDATED RESUMES TO: MAMCDONOUGH @ ACTALENTSERVICES.COM </p><p style="text-align: center;">OR TEXT MARISA TO SETUP A PHONE INTERVIEW: 330. 397. 1302</p><p><br></p><p><strong><u>Job Description</u></strong></p><p>The Lab Technician performs each essential duty safely, satisfactorily, and in a timely manner. This role involves understanding and following batch tickets with high accuracy, performing complex testing processes on production batches, and maintaining a clean and organized work environment.</p><p><br></p><p><strong><u>Responsibilities</u></strong></p><ul><li>Understand and follow a batch ticket (recipe) with high degree of accuracy for weights and measurements.</li><li>Perform a wide variety of complex testing processes on production batches to measure product’s physical or chemical characteristics, including viscosity, weight per unit of measure, flow, gloss, and color characteristics.</li><li>Test materials from suppliers and production batches.</li><li>Perform standard testing procedures, including preparation of materials with attention to detail and high quality.</li><li>Follow daily work plan for Lab Work Request or project plan.</li><li>Accurately document work in lab notebooks, whether physical or electronic.</li><li>Recognize roadblocks or anomalies and resolve them or communicate concerns with a chemist in a timely manner.</li><li>Ensure raw materials are available and correctly labeled.</li><li>Correctly label and mail samples.</li><li>Maintain a clean and organized work environment.</li><li>Tint batches without assistance.</li><li>Calculate resin composites.</li><li>Maintain QC records using a web-based computer system.</li><li>Prepare records for submission.</li><li>Perform tests using lab equipment such as viscosity, pH, weight per gallon, and % solids.</li><li>Conduct draw downs and use ovens.</li><li>Maintain and perform calibrations on machines.</li></ul><p><strong><u>Essential Skills</u></strong></p><ul><li>Chemistry</li><li>Laboratory skills</li><li>Color matching</li><li>Quality control</li><li>Lab Technician experience</li></ul><p><strong><u>Additional Skills &amp; Qualifications</u></strong></p><ul><li>Not color blind</li><li>Prior quality/wet lab experience or entry-level graduate with AS or BS in Science</li><li>Prior experience with color matching is a plus</li><li>Experience working with paint, pigments, and coatings</li><li>Industrial lab experience doing basic wet chemistry, including viscosity, pH, and % solids</li></ul><p><strong><u>Work Environment</u></strong></p><p>This role is based in an industrial lab environment within the plant. Personal protective equipment (PPE) such as lab coats and safety glasses will be provided. On the first day of training, steel-toed boots/shoes will be required, and reimbursement will be provided. The facility may have strong smells of chemicals and paint, so applicants should not be sensitive to those. The lab is large, with at least five people on each shift at all times.</p>

<p><strong><em>Actalent is hiring for an exciting opportunity in natural sciences – Seed Lab Technician</em></strong></p><p><br></p><p>Are you passionate about hands-on science and ready to make an impact in agricultural research? Join a dynamic team where your attention to detail and curiosity will help shape the future of seed science. <strong><u>Great opportunity for people looking for an entry level lab position!</u></strong></p><p><br></p><p><strong>Key Responsibilities</strong>:</p><ul><li>Conduct visual inspections of seed samples for quality and consistency</li><li>Perform essential lab tests including pH, protein assays, moisture analysis, and titrations</li><li>Execute warm and cool germination tests</li><li>Carry out purity analysis and precise seed counts</li><li>Organize and implement standardized sampling procedures</li></ul><p><strong>Schedule Details:</strong></p><ul><li>Standard Hours: Monday–Friday | 7:00 AM – 5:30 PM</li><li>Peak Season (Nov–Jan):Two shifts available<ul><li>7:00 AM – 5:30 PM</li><li>5:00 PM – 3:30 AM</li></ul></li><li>Spring Season (Feb–May): May include weekend work</li><li>Flexibility for 1st or 2nd shift is required</li></ul><p><strong>Compensation:</strong></p><ul><li>$16.00 per hour</li><li>Benefits: Health, dental, vision</li><li>401K</li></ul><p><strong>Qualifications:</strong></p><ul><li>High School Diploma (Required)</li><li>Valid Passport or Birth Certificate required for onboarding</li><li><strong>Must be available to start on September 2</strong></li></ul><p><strong><em>Ready to start your lab career? Apply today! Multiple spots available!</em></strong></p>

<h1><strong>Apply today to join a company that strives to nourish the community with quality dairy products! </strong></h1><p>As a Quality Lab Technician, you will play a crucial role in ensuring the safety and quality of dairy products. You will assist in the sanitation of the lab and equipment, conduct various tests and evaluations on products, and collaborate with the quality team to uphold high standards in food safety and quality control.</p><h2>Responsibilities</h2><ul><li>Sanitize the lab and equipment to maintain a clean working environment.</li><li>Prepare dilutions of milk and conduct chemical testing.</li><li>Verify the success of pasteurization by plating samples for E. coli and bacteria testing.</li><li>Incubate samples for further analysis.</li><li>Conduct testing of in-house water (city water) and perform sensory testing on milk, chocolate milk, and ice cream.</li><li>Package and label samples for external shipment.</li><li>Engage with Continuous Improvement (CI) initiatives and promote a culture of safety.</li><li>Perform sensory evaluations of product samples, both fresh and at shelf life.</li><li>Prepare samples, media, and solutions for chemical, physical, and microbiological analysis.</li><li>Conduct accurate microbiological analysis, including Coliform, Standard Plate Count, Yeast &amp; Mold.</li><li>Perform chemical and physical analyses such as Antibiotics, Freeze point analysis, Phosphatase, butterfat, Total solids, Brix, Titratable Acidity, and Vitamin analysis.</li><li>Operate, calibrate, maintain, and troubleshoot laboratory equipment like Foss FT120, Cryoscope, Horiba, Brix, and pH meters.</li><li>Perform quality checks and escalate any non-compliance issues to the quality leadership team.</li><li>Conduct pre-operational and sanitation checks, including visual inspections and ATP swabbing.</li><li>Check finished product labels, coding, and packaging.</li><li>Collect, transport, store, test, and dispose of samples properly.</li><li>Maintain the Environmental Monitoring and Allergen Programs, including air and water quality assessments.</li><li>Coordinate sampling and shipments with third-party laboratories and handle customer requests.</li><li>Maintain an inventory of laboratory supplies, ensuring proper stock levels and rotation.</li><li>Organize and maintain production and quality control records in compliance with regulations.</li><li>Enter data and create reports promptly and accurately.</li><li>Ensure records are accurate and legible, adhering to Good Documentation Practices (GDPs).</li><li>Maintain laboratory cleanliness and follow Good Laboratory Practices (GLPs).</li><li>Follow all Good Manufacturing Practices (GMPs) and established quality and safety policies.</li><li>Participate in laboratory proficiency programs and identify process improvements.</li><li>Orient and instruct others in job duties when required.</li><li>Assist Quality Assurance Supervisor and Manager in special projects and other assigned duties.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor&#39;s degree in Microbiology, Food Science, Agriculture, or a related science field preferred.</li><li>Knowledge of Good Laboratory Practices (GLPs) and Good Documentation Practices (GDPs).</li><li>Understanding of quality assurance and HACCP systems.</li><li>Ability to work well in a team and independently.</li><li>Strong time management and organizational skills.</li><li>Proficient in Microsoft Outlook, Word, Excel, and PowerPoint.</li><li>Excellent interpersonal, written, and verbal communication skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in the microbiology field, either academic or industry-related.</li><li>Experience demonstrating teamwork, time management, and process improvement abilities.</li><li>Students from UC Davis are a plus.</li><li>Self-starter with the ability to complete tasks without close supervision.</li><li>Exposure to the dairy industry is beneficial.</li></ul><h2>Work Environment</h2><p>This position is a night shift, working from 6:00 pm - 2:30 am. The role involves working 70% in the lab and 30% in the plant/data/paperwork. The quality team consists of three technicians, an SQF coordinator, and a QA manager. You will primarily work independently in the lab, with some crossover with other technicians at the <span style="color: rgb(8, 7, 7); background-color: none;">beginning</span> and end of your shift. Support is available from the QA manager or SQF coordinator if needed. Occasionally, there may be collaboration with the sanitation supervisor.</p>

<h2 style="text-align: center;"><strong>**Immediate Opening: Quality Laboratory Technician**</strong></h2><p style="text-align: center;"><strong>Interested in this role? </strong>Reach out directly to apply <strong>TODAY </strong>to <strong>Grace Williams </strong>at <strong>grawilliams@actalentservices .com</strong></p><h2><br></h2><p><br></p><p><strong>Position Summary</strong></p><p>Are you passionate about food safety, precision, and laboratory excellence? Join our team as a <strong>Quality Control Assurance Laboratory</strong></p><p><strong>Technician</strong> and play a vital role in upholding the highest standards of product quality and regulatory compliance. We are looking for a detail-oriented and dedicated professional to support our facility through comprehensive testing of finished products, packaging, and raw materials. In this hands-on role, you’ll dive into testing finished products, packaging, and raw materials—making sure everything is up to spec before it reaches our customers. You’ll be a key player in a fast-paced, collaborative environment where your work directly impacts the safety and satisfaction of consumers. This is an exciting opportunity to support finished product, packaging, and raw material testing within a dynamic production environment.</p><p><br></p><p>If you&#39;re detail-driven, science-savvy, and ready to make a difference in a dynamic production setting, we’d love to meet you!</p><p><br></p><p><strong>Key Responsibilities</strong></p><ul><li>Conduct laboratory testing to ensure products meet established specifications</li><li>Accurately enter and consolidate lab data, and report findings to operational teams</li><li>Support internal audits and maintain laboratory equipment</li><li>Participate in cross-training within chemistry labs to enhance team flexibility</li><li>Test finished goods, raw materials (milk, oil, corn syrup), and packaging for compliance.</li><li>Conduct cream release, component, and identity (ID) testing on incoming materials.</li><li>Execute quality control tests on raw, in-process, and finished products.</li><li>Perform mathematical calculations related to quality assurance.</li><li>Calibrate Charm SL equipment and prepare FT2 cleaning and zero solutions.</li><li>Maintain a clean, organized, and safe laboratory environment in compliance with safety and contamination policies.</li><li>Monitor and record temperatures of refrigerators and incubators daily.</li><li>Manage sample receipt, handling, and testing for finished products, raw materials, and packaging.</li><li>Record, review, and verify data using Good Documentation Practices (GDP) and Good Laboratory Practices (GLP).</li><li>Execute laboratory procedures and the Internal Control Plan (ICP) with accuracy.</li><li>Enter test results and perform all required transactions in SAP and related data systems.</li><li>Consolidate, trend, and report laboratory data to operations; escalate out-of-spec results promptly.</li><li>Manage inventory and ordering of lab consumables.</li><li>Revise protocols and process flows as needed.</li><li>Conduct routine quality and food safety audits.</li><li>Support continuous improvement initiatives.</li><li>Obtain and maintain Appendix N certification; complete annual split samples.</li></ul><p><strong>Qualifications</strong></p><ul><li>Bachelor’s degree in a life science field (e.g., Biology, Chemistry, Food Science).</li><li>Understanding of GMP, HACCP, SQF, and food safety regulations.</li><li>Familiarity with wet chemistry, titration, and chemical testing.</li><li>Ability and understanding to follow quality assurance checks/inspections/lab tests</li></ul><p><br></p><p><strong>Work Environment</strong></p><ul><li>Time split between lab and production floor to conduct sampling and testing.</li><li>Tasks include sensory evaluation, instrument calibration, and bulk material testing (milk, sugar, oil).</li></ul><p><br></p><p><strong><u>INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION:</u></strong></p><p><em><u>*Interview availability this week*</u></em></p><ul><li>I am scheduling interviews for this position and conducting phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to <strong>Grace Williams</strong>.</li><li><strong>HOW TO APPLY DIRECTLY: </strong>Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to <strong>grawilliams@actalentservices. com </strong>or call me directly at <strong>(317-567 -6610)</strong></li></ul><h2><br></h2>

Quality Laboratory Tech - HIRING NOW

<h1 style="text-align: center;"><strong>Job Title: Quality Laboratory Technician</strong></h1><p style="text-align: center;"><em>**INTERVIEWS AVAILABLE THIS WEEK**</em></p><p style="text-align: center;"><strong>﻿Interested in this role? </strong>Reach out directly to <strong>mrichey<em>@actalentservices .com or CALL 317 567 </em>6591 </strong>with an updated resume to apply (HIRING NOW)</p><p style="text-align: center;">**Located In Lafayette*</p><h2>Job Description</h2><p>The Quality Laboratory Technician plays a crucial role in ensuring the highest standards of quality assurance and control within the laboratory. This position involves working primarily with sweeteners, corn syrups, and sugar products, which are processed into corn sweeteners such as high fructose corn syrup, sugar, and starches for human and animal feed. The laboratory is divided into chemistry and microbiology sections, where technicians perform extractions and work on liquid products.</p><p><br></p><h2>Responsibilities</h2><ul><li>Prepare and analyze various final product and in-process samples using analytical instruments and wet chemistry techniques.</li><li>Facilitate plant process flow by providing timely and accurate analysis results.</li><li>Post analysis results into data systems and communicate findings to plant personnel.</li><li>Recognize abnormal findings and collaborate with process teams to resolve issues.</li><li>Conduct final QA/QC of outbound shipments and document results.</li><li>Follow established analysis methodologies and perform basic laboratory equipment maintenance.</li><li>Support other departments with analytical and project-based efforts on an ad hoc basis.</li><li>Ensure adherence to all company policies and procedures and demonstrate core values.</li><li>Support a 24/7 process by working a rotating shift, including nights, weekends, and holidays.</li><li>Advance through skill block system, achieving four &#39;operate&#39; skill blocks and a &#39;basic&#39; skill block.</li><li>Perform other duties as assigned.</li></ul><h2>Essential Skills</h2><ul><li>A 4-year degree in Chemistry, Biology, or another relevant scientific discipline.</li><li>Ability to prepare and analyze in-process and finished goods using various laboratory methodologies and equipment.</li><li>Experience and understanding of HPLC, GC, AA, NIR, pH, and other laboratory techniques.</li><li>Willingness to support a 24/7 process and work rotating shifts, including nights, weekends, and holidays.</li><li>Ability to multitask, prioritize, and maintain attention to detail.</li><li>Excellent written and verbal communication skills.</li><li>Self-starting and detail-oriented with good troubleshooting skills.</li><li>Strong computer skills, including proficiency in Microsoft Office Applications.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Knowledge and experience with SAP is a plus.</li></ul><h2>Work Environment</h2><p>Candidates will work 12-hour shifts, typically 3 days on and 3 days off, rotating between day and night shifts (e.g., 5 AM to 5 PM for 3 days, off for 3 days, then 5 PM to 5 AM for 3 days, off for 3 days). The role requires standing for extended periods, and the dress code includes jeans and a t-shirt.</p><p><br></p><p><strong>INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION:</strong></p><p>I am scheduling interviews for this position <strong>ASAP </strong>and conducting phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to <strong>Max Richey</strong></p><p><strong>HOW TO APPLY DIRECTLY: </strong>Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to <strong><u>mrichey@actalentservices. com or CALL 317 567 6591</u></strong></p>

Quality Laboratory Technician

<p style="text-align: center;"><strong><em>HIRING NOW</em>: </strong>﻿ <strong>Food Safety &amp; Quality Lead</strong></p><p style="text-align: center;"><em>**INTERVIEWS AVAILABLE THIS WEEK**</em></p><p style="text-align: center;"><strong>﻿Interested in this role? </strong>Reach out directly to <strong>mrichey<em>@actalentservices .com or CALL 317 567 </em>6591 </strong>with an updated resume to apply (HIRING NOW)</p><p style="text-align: center;">*Located In Wolcott*</p><p><br></p><h2>Job Description</h2><p>The Food Safety &amp; Quality Supervisor is entrusted with overseeing daily operations related to food safety and quality assurance in a food manufacturing environment. This role is pivotal in ensuring compliance with regulatory standards and internal protocols, supporting continuous improvement initiatives, and fostering a robust culture of food safety across the facility.</p><p><br></p><h2>Responsibilities</h2><ul><li>Manage and maintain food safety and quality programs, including HACCP, GMPs, SSOPs, and allergen control.</li><li>Conduct facility inspections, internal audits, and risk assessments to ensure compliance with USDA, FDA, and other applicable regulations.</li><li>Supervise and train quality assurance staff on food safety procedures and documentation.</li><li>Investigate and resolve quality issues, customer complaints, and non-conformances.</li><li>Maintain accurate records of inspections, testing, and corrective actions.</li><li>Collaborate with cross-functional teams to support product launches and process improvements.</li><li>Prepare for and participate in third-party audits and regulatory inspections.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor’s degree in Food Science, Microbiology, or a related field.</li><li>Minimum of 3 years of experience in food manufacturing, preferably in a USDA-regulated facility.</li><li>Certifications such as PCQI, HACCP, or SQF Practitioner are preferred.</li><li>Strong understanding of food safety regulations and quality systems.</li><li>Excellent communication, leadership, and analytical skills.</li><li>Proficiency in Microsoft Office and quality management software.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in food &amp; beverage manufacturing, specifically within quality.</li><li>Certifications like HACCP Certification, PCQI Certification, SQF Practitioner, or other GSQI.</li><li>Experience with food safety standards.</li><li>Knowledge of chemistry and laboratory procedures.</li></ul><h2>Work Environment</h2><p>The position is within a start-up manufacturing company producing egg replacement wraps. The work culture is collaborative, with close relationships across departments, especially between R&amp;D and quality teams. The supervisor will oversee five lab technicians across multiple shifts. The typical work schedule is Monday to Friday, from 7 AM to 4 PM, with occasional on-call rotations. The environment supports growth, with opportunities to gain certifications internally, such as PCQI.</p><p><br></p><p><strong>INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION:</strong></p><ul><li>I am scheduling interviews for this position <strong>ASAP </strong>and conducting phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to <strong>Max Richey</strong></li><li><strong>HOW TO APPLY DIRECTLY: </strong>Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to <strong><u>mrichey@actalentservices. com or CALL 317 567 6591</u></strong></li></ul>

Quality Lead

<h1 style="font-weight: 700;">Job Title: Quality Lead</h1><br><h2>Job Description</h2><p>The Quality Lead is responsible for ensuring product integrity throughout the production process. This role is ideal for candidates with strong attention to detail, hands-on experience with precision measurement tools, and the ability to communicate effectively with internal teams and external partners.</p><br><h2>Responsibilities</h2><ul><li>Conduct incoming, in-process, and final inspections using tools such as calipers, micrometers, microscopes, and vision systems for micro parts.</li><li>Perform lab-based measurements including pH testing, viscosity, and moisture analysis using specialized equipment.</li><li>Execute pull force and burst testing to verify product durability and compliance.</li><li>Schedule and coordinate specialized testing with external laboratories when needed.</li><li>Ensure product quality through detailed visual assessments before release.</li></ul><h2>Essential Skills</h2><ul><li>2-5 years of experience with hands-on inspection.</li><li>Strong communication and reporting skills.</li><li>Experience within a Medical Device/Pharmaceutical setting is preferred but not required.</li><li>Proficiency in inspection, testing, and metrology.</li><li>Hands-on experience with precision measurement tools such as calipers, micrometers, and microscopes.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in quality inspection and visual assessment.</li><li>Knowledge of testing methods including pH testing, moisture testing, pull force testing, and burst testing.</li></ul><h2>Work Environment</h2><p>The position is 100% onsite with a start time of 6am. The team consists of 80 employees across two locations, with 5 dedicated to quality (including 3 technicians). The primary worksite is the production facility located at 510 S Vermont Ave, Glendora, with some time spent at the headquarters at 2035 E Financial Way, Glendora. The company offers a supportive team environment, early shift schedules, and a strong focus on work-life balance.</p><br>

<h1 style="font-weight: 700;">Job Title: Quality Lead</h1><br><h2>Job Description</h2><p>We are seeking a dedicated Quality Lead for the 3rd shift from 10pm to 6:30am. The role involves reviewing and approving records to ensure compliance with established standards. This position requires a proactive individual to identify deviations and initiate corrective actions, including conducting root cause analyses.</p><br><h2>Responsibilities</h2><ul><li>Identify deviations and initiate Non-Conformance and Corrective Action (CAPA) investigations.</li><li>Coordinate completion of CAPA investigations including root cause analyses.</li><li>Manage disposition of raw materials and products as Hold, Release, or Quarantine.</li><li>Conduct basic food safety, cGMP, and quality-related training for new hires.</li><li>Assist with the development of SOPs related to manufacturing processes.</li><li>Provide support during audits by regulatory and third parties.</li><li>Conduct and coordinate environmental testing as part of the Environmental Monitoring Program.</li><li>Collect raw materials for testing and sample finished products.</li><li>Evaluate sensory characteristics for product approval and shelf life studies.</li><li>Work with production personnel to correct processes if the product is out of compliance.</li><li>Convey test results to the appropriate personnel and follow up if needed.</li><li>Complete audits based on the production schedule.</li><li>Conduct and coordinate facility environmental testing.</li><li>Promote and follow GMPs for the facility.</li></ul><h2>Essential Skills</h2><ul><li>FDA regulations</li><li>Quality control and quality assurance</li><li>GMP</li><li>HACCP</li><li>SQF</li><li>GFSI</li><li>PCQI</li><li>Food safety</li><li>Food manufacturing</li><li>Batch record review</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>3 plus years of Food or GMP Manufacturing Quality experience</li><li>Degree in the sciences is preferred</li><li>SQF, HACCP, GFSI, or PCQI training/experience is a plus</li></ul><h2>Work Environment</h2><p>The position is based in a food manufacturing plant with a balanced 50/50 split between lab and floor work. Initial training will be provided for a period of 3-6 months.</p><br>

<p><strong><u>Job Summary </u></strong></p><p>This role involves evaluating batches, finished goods, and raw materials according to specifications while maintaining accurate records and generating certificates of analysis. It requires coordination of equipment sanitation and swab testing, conducting in-house and customer sanitation audits, and initiating and updating set-up sheets.</p><p><br></p><p><strong><u>Responsibilities </u></strong></p><ul><li>Serve as back-up to the QC Supervisor.</li><li>Calibrate and verify laboratory equipment.</li><li>Arrange delivery of samples for external testing.</li><li>Participate in audits and special projects.</li><li>Perform daily scale and metal detector checks.</li><li>Assess production lines for quality procedures.</li><li>Investigate customer complaints.</li><li>Audit sanitation of blending and production equipment.</li><li>Assist in operations and administrative tasks.</li><li>Support Kosher and Halal certification maintenance.</li><li>Review ingredients and finished products for age.</li><li>Participate in recall and mock recall procedures.</li><li>Research and implement continuous improvement efforts.</li><li>Enter production data into the database system.</li></ul><p><strong><u>Qualifications</u></strong></p><ul><li>Minimum of 2 years of experience in quality control in the food industry or related field.</li><li>Experience with training quality technicians.</li><li>Knowledge of GMP guidelines.</li><li>Proficiency in computer skills.</li><li>Quality assurance and HACCP understanding.</li></ul><p><strong><u>About Actalent</u></strong></p><p>Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.</p><p><br></p><p><strong><u>Diversity, Equity &amp; Inclusion</u></strong></p><p>At Actalent, Diversity And Inclusion Are a Bridge Towards The Equity And Success Of Our People. DE&amp;I Are Embedded Into Our Culture Through:</p><p><br></p><ul><li>Hiring diverse talent</li><li>Maintaining an inclusive environment through persistent self-reflection</li><li>Building a culture of care, engagement, and recognition with clear outcomes</li><li>Ensuring growth opportunities for our people</li></ul>

<h1><strong>Quality Manager</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a dedicated Quality Manager to implement, execute, and promote food safety practices within our products. The successful candidate will uphold Good Manufacturing Practices (GMPs), adhere to Standard Operating Procedures (SOPs), and maintain compliance with regulatory standards such as FDA cGMP, EXCiPACT, and BRC. You will lead quality program planning to ensure our product and quality systems meet customer specifications and regulatory requirements.</p><p><br></p><h2>Responsibilities</h2><ul><li>Direct and oversee the quality program to ensure compliance with customer specifications and regulatory standards.</li><li>Manage lab operations, including planning and scheduling laboratory coverage and approving timecards.</li><li>Provide developmental and annual training to the quality team to enhance their skills in quality techniques and troubleshooting.</li><li>Ensure a safe working environment for all quality employees.</li><li>Communicate facility quality performance through various formats to management, operations, and warehouse staff.</li><li>Coordinate and conduct development, maintenance, and validation of test methods.</li><li>Assist in developing, updating, and maintaining product specifications.</li><li>Support engineering and technology teams in new product developments and process improvements.</li><li>Maintain Lab QMS System (LX-400) databases.</li><li>Research, propose, purchase, and set up new instrumentation within budget and timeframe.</li><li>Propose, write, and review quality control Standard Operating Procedures.</li><li>Perform statistical analysis of test results for internal trending.</li><li>Provide backup support for QA and QC Coordinators and Chemical Analysts as needed.</li><li>Collaborate with various departments to lead projects focusing on cost savings, quality improvements, and new product development utilizing Lean Six Sigma methodologies.</li><li>Work with plant leadership to ensure project outcomes meet quality standards.</li><li>Perform additional duties as defined by the manager.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor’s Degree in Food Science, Engineering, Life Sciences, or a similar field.</li><li>Five years of experience in quality and/or regulatory leadership in a food manufacturing setting.</li><li>Experience with food safety/quality programs, including HACCP, GMPs, SPC, and exposure to Continuous Improvement programs like Six Sigma and TQM.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Strong leadership and communication skills.</li><li>Ability to manage and develop a team effectively.</li><li>Proficiency in statistical analysis and quality management systems.</li></ul><h2>Work Environment</h2><p>This role is based in an industrial food manufacturing facility. You will lead a team comprising a Quality Supervisor, Quality Control Technicians, a Document Control Specialist, and a QA Coordinator. The position requires overseeing three process areas for sample collection and maintaining alignment with company directives. The position is open due to the current quality manager&#39;s notice, and we are seeking to fill it as soon as possible. Shift flexibility is available. The team is responsible for critical process characteristics, standards, audits, and complaint resolutions, ensuring that team goals align with the company&#39;s objectives.</p>

Quality Manager

<h1 style="font-weight: 700;">Job Title: Quality Manager</h1><br><h2>Job Description</h2><p>Responsible for overseeing the Quality Department and direct reports, ensuring the overall quality of our products.</p><br><h2>Responsibilities</h2><ul><li>Train employees on quality requirements.</li><li>Conduct internal auditing and day-to-day inspections.</li><li>Oversee product testing and manage employee training and audits.</li><li>Address customer issues and conduct customer audits.</li><li>Perform supplier audits and ensure compliance.</li><li>Conduct IPC training and certification.</li><li>Manage PPAP and FAI reporting.</li><li>Handle NCM/RMA disposition.</li><li>Develop tests on automated harness testers.</li><li>Issue non-conformances and maintain a log for customer reports.</li></ul><h2>Essential Skills</h2><ul><li>Minimum 3 years of quality experience as a lead.</li><li>Minimum 3 years of experience in a relevant environment.</li><li>Minimum 3 years of experience working with and documenting PPAPs.</li><li>Minimum 1 year of experience working with cables and wiring.</li><li>Ability to interpret drawings within AutoCAD and blueprints.</li><li>Minimum 1 year of experience leading a team.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with quality inspection, harness, and cable harness.</li></ul><h2>Work Environment</h2><p>This role is within a small, growing company involved in major markets including medical, automotive, agriculture, and hydraulic power. The company employs approximately 35-40 individuals. The work schedule is Monday to Friday with occasional Saturdays. Summer hours (Memorial Day to Labor Day) are 6am-3pm Monday through Thursday and 6am-Noon on Friday. Non-summer hours are 6am-2:30pm Monday through Friday. The company is ISO 9001:2015 certified and practices Lean Manufacturing.</p><br>

<h1><strong>Job Title: Quality Manager</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking an experienced Quality Manager to lead and maintain our Quality Management System (QMS) in compliance with FDA and other regulatory requirements. This role involves managing audits, overseeing quality processes, and collaborating with cross-functional teams to ensure product excellence.</p><p><br></p><h2>Responsibilities</h2><ul><li>Lead and maintain the company’s QMS in compliance with FDA and other regulatory requirements.</li><li>Manage internal and external audits, including FDA inspections and ISO certification audits.</li><li>Oversee CAPA, nonconformance, and complaint handling processes.</li><li>Collaborate with cross-functional teams (R&amp;D, Manufacturing, Regulatory) to ensure quality is built into every stage of the product lifecycle.</li><li>Develop and monitor quality metrics and KPIs; report findings to leadership.</li><li>Lead training programs on quality standards, procedures, and best practices.</li><li>Manage document control, change control, and risk management processes.</li><li>Supervise quality assurance and quality control staff.</li><li>Other duties and special projects as assigned.</li></ul><h2>Essential Skills</h2><ul><li>Quality engineering</li><li>Quality assurance</li><li>Root cause analysis</li><li>Medical device industry experience</li><li>CAPA</li><li>Quality management</li><li>AS9100</li><li>Quality management system</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in Engineering, Life Sciences, or related field (Master’s preferred).</li><li>5+ years of experience in quality management within the medical device industry.</li><li>Strong knowledge of FDA QSR and risk management (ISO standards).</li><li>Experience with CAPA, root cause analysis, and audit readiness.</li><li>Excellent leadership, communication, and problem-solving skills.</li><li>ASQ certifications (e.g., CQE, CQA) are a plus.</li></ul><h2>Work Environment</h2><p>This position involves working closely with cross-functional teams and requires strong collaboration skills. The work environment prioritizes compliance with regulatory standards and continuous improvement. Typical office attire is expected.</p>

<h1><strong>Job Title: Quality Manager – Automotive Seating (EV)</strong></h1><p><br></p><h2>Job Description</h2><p>A global automotive supplier seeks a Quality Manager to lead and develop a team of quality professionals at one of its high-impact EV seating manufacturing sites in either Champaign, IL or Mesa, AZ. This is a critical leadership role with direct visibility to site leadership and OEM customers.</p><p><br></p><h2>Responsibilities</h2><ul><li>Lead and develop a team of up to 10 quality professionals, including team leads, specialists, and assistant managers.</li><li>Oversee quality documentation, audits, and compliance with customer and industry standards.</li><li>Collaborate cross-functionally with production and engineering teams to drive continuous improvement.</li><li>Serve as the primary quality contact for OEM customers.</li><li>Report directly to the site CEO.</li></ul><h2>Essential Skills</h2><ul><li>5+ years of experience in a quality leadership role within automotive manufacturing.</li><li>Proficiency in GD&amp;T, color measurement systems, and quality documentation.</li><li>Must pass a color vision assessment.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree required; Master’s preferred.</li><li>Experience in seating systems and/or EV manufacturing strongly preferred.</li><li>Experience with seating manufacturing and Tier 1 Automotive experience is a plus.</li></ul><h2>Work Environment</h2><p>The role is 100% onsite, first shift, from Monday to Friday in a fast-paced, hands-on manufacturing setting. The company values safety, structure, and continuous improvement, with a strong emphasis on safety, health, and environmental responsibility. They have implemented international standards such as ISO and conduct monthly on-site safety inspections. The culture values visibility, accountability, and direct leadership.</p>

<h1><strong>Job Title: Quality Manager</strong></h1><p><br></p><h2>Job Description</h2><p>As the Quality Assurance Manager of a world-leading manufacturer of foodservice equipment known for its innovation and commitment to quality, you will be responsible for all quality-related standard operating procedures, internal and external audits in adherence with internal and regulatory standards. The function of the Quality Assurance Manager is to promote quality achievement and performance improvement throughout the organization.</p><p><br></p><h2>Responsibilities</h2><ul><li>Manage the quality assurance department, directing the work of quality technicians and any other personnel, to satisfy the quality requirements for current business and future improvements.</li><li>Develop and execute annual quality goals and objectives that align with overall company goals and long-term strategic concerns.</li><li>Setup and maintain ISO 9001 certification and adhere to the quality system.</li><li>Educate and train employees on their impact in the quality management system, including quality matters, protocol, and procedures.</li><li>Actively direct the corrective actions system for customer complaints, warranties, returns, and internal processes.</li><li>Work with all departments to develop documentation of processes and procedures.</li><li>Lead the development of quality and improvement plans that will impact the overall cost of products.</li><li>Conduct audits, including closing out audit findings, creating audits, finding reports, and determining proper corrective and preventive actions.</li><li>Prepare the organization for audits and certifications.</li><li>Assist the management team and provide support as necessary.</li><li>Nurture a philosophy of a quality culture.</li><li>Follow and comply with all environmental, safety, and work rules and regulations.</li><li>Evaluate, redesign as needed, and implement organizational systems.</li><li>Provide quality-based direction to production staff in all facets of operations to ensure quality and, where applicable, ensure the safe, efficient, and effective operations of the facility.</li><li>Develop positive relationships and effective lines of communication with suppliers.</li><li>Manage the Supplier Quality metrics, including Non-Conformance Tracking (MRB), Supplier Corrective Action Requests (SCAR), and Corrective Action and Preventive Action.</li><li>Work closely with the Purchasing Group to establish and maintain a Supplier Quality Scorecard.</li><li>Participate in new product introduction or product change projects, assuring that all requisite quality characteristics and requirements are met.</li></ul><h2>Essential Skills</h2><ul><li>At least 7-10 years of relevant experience in a manufacturing-based business.</li><li>Specific experience and training in quality assurance and control shop inspection practices required.</li><li>Demonstrated experience working with contract manufacturers, suppliers, or distributors.</li><li>Experience in ISO 9001 Quality systems, including systems auditing.</li><li>Intermediate skills with Microsoft Office Word, Excel, and PowerPoint.</li><li>Knowledge of quality methods, tools, and instruments such as 5 Why analysis and Ishikawa Diagram.</li><li>Demonstrated leadership skills and communication skills with all levels of employees.</li><li>Extensive knowledge of Quality Management systems and planning techniques.</li><li>Experience in developing and implementing training for inspection, quality system, and Total Quality Management methods.</li><li>Functional knowledge of statistical concepts as applied to the field of Quality Control.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in Quality or an Engineering Discipline, Master&#39;s preferred.</li><li>Strong experience in quality systems is preferred.</li><li>Quality experience at a foodservice equipment manufacturing company is preferred.</li></ul><h2>Work Environment</h2><p>Onsite, office-based position requiring meetings and collaboration on the factory floor.</p>

<h1 style="font-weight: 700;">Job Title: Quality Technician</h1><br><h2>Job Description</h2><p>As a Quality Technician, you will be responsible for performing in-process and final product inspections, conducting tests to ensure compliance with specifications, maintaining and calibrating testing equipment, documenting and reporting quality issues, working with production teams to resolve quality concerns, and assisting in audits and continuous improvement initiatives.</p><br><h2>Responsibilities</h2><ul><li>Perform in-process and final product inspections.</li><li>Conduct tests to ensure compliance with specifications.</li><li>Maintain and calibrate testing equipment.</li><li>Document and report quality issues.</li><li>Collaborate with production teams to resolve quality concerns.</li><li>Assist in audits and continuous improvement initiatives.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in inspection and laboratory techniques.</li><li>Experience in quality control and quality assurance.</li><li>Knowledge of GMP practices.</li><li>Understanding of chemistry and biology principles.</li><li>Ability to perform quality inspections and checks.</li><li>Skill in visual inspection and wet chemistry.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Associate&#39;s or Bachelor&#39;s degree in Sciences or equivalent.</li><li>Minimum of 2 years of quality experience within manufacturing.</li></ul><h2>Work Environment</h2><p>The position is based at a coated products manufacturing site, primarily in a laboratory setting. Employees will work a 12-hour rotating schedule, including both day and night shifts. The role involves working 3-4 shifts per week, with an advanced schedule provided 4 weeks ahead to cover planned vacations and projects. Expect a block of 6 days off each month, and the possibility of working additional Saturdays if operations require. Sunday shifts are voluntary and compensated at double time, typically reserved for tenured staff. Employees enjoy 17 six-day off stretches throughout the year, 10 paid holidays, and 2 floating holidays.</p><br>

Quality Manufacturing Technician

<p><strong>Description</strong></p>
					<p>	Ensure facility compliance with cGMP regulations (21 CFR Part 111 for dietary supplements, 21 CFR 210/211 for OTC drugs if applicable, and ISO 22716 for skin care).
	Maintain and oversee the Quality Management System (QMS), including SOPs, work instructions, and quality manuals.
	Manage regulatory inspections (FDA, state, third-party audits) and coordinate responses to findings.
	Stay updated on relevant regulatory changes and ensure facility compliance.
	Review and approve Master Manufacturing Records (MMRs) and Batch Production Records (BPRs) for accuracy and compliance.
	Oversee and approve in-process checks (pH, viscosity, microbial limits, fill weights).
	Ensure that line clearance and changeover procedures are properly executed.
	Supervise incoming raw material testing (identity, potency, microbiological, heavy metals if applicable).
	Oversee finished product testing to ensure products meet specifications.
	Review and approve Certificates of Analysis (CoA) from third-party labs.
	Approve and maintain the Approved Supplier Program.
	Conduct supplier qualifications, audits, and periodic reviews.
	Ensure proper raw material traceability and adherence to quality specifications.
	Investigate deviations, non-conformances, and customer complaints.
	Lead root cause analysis (RCA) and implement Corrective and Preventive Actions (CAPA).
	Manage change control for processes, materials, and equipment affecting product quality.
	Train staff on cGMP, SOPs, hygiene, and quality standards.
	Maintain training records and ensure ongoing competency of production and quality teams.
	Ensure proper documentation practices (GDP).
	Maintain and archive all quality records, batch documentation, and testing results per regulatory requirements.
	Monitor and ensure compliance with sanitation and cleaning validation protocols.

	Oversee environmental monitoring for microbial contamination (particularly for liquid products).
	Make final product disposition decisions (release, reject, or hold).
	Participate in product recall investigations and ensure recall procedures are in place.
	Identify process improvements to enhance product quality, efficiency, and compliance.
	Participate in cross-functional meetings to ensure quality considerations are integrated into production planning.</p>
					<p><strong>Skills</strong></p>
					<p>Gmp, fda, audit, cgmp</p>
					
					
					<p><strong>Additional Skills &amp; Qualifications</strong></p>
					<p>-	Knowledge of Excel, Word, and Adobe software.
-	Communication and management skills.
-	Ability to manage, carryout, and prioritize departmental functions.
-	Ability to see areas that need improvement and to address them.
-	Extensive <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">background</span></span></span></span> in quality systems and food and beverage manufacture.</p>
					<p><strong>Experience Level</strong></p>
					<p>Expert Level</p>

Quality Operations Manager

<p><strong>Description</strong></p>
					<p>	Ensure facility compliance with cGMP regulations (21 CFR Part 111 for dietary supplements, 21 CFR 210/211 for OTC drugs if applicable, and ISO 22716 for skin care).
	Maintain and oversee the Quality Management System (QMS), including SOPs, work instructions, and quality manuals.
	Manage regulatory inspections (FDA, state, third-party audits) and coordinate responses to findings.
	Stay updated on relevant regulatory changes and ensure facility compliance.
	Review and approve Master Manufacturing Records (MMRs) and Batch Production Records (BPRs) for accuracy and compliance.
	Oversee and approve in-process checks (pH, viscosity, microbial limits, fill weights).
	Ensure that line clearance and changeover procedures are properly executed.
	Supervise incoming raw material testing (identity, potency, microbiological, heavy metals if applicable).
	Oversee finished product testing to ensure products meet specifications.
	Review and approve Certificates of Analysis (CoA) from third-party labs.
	Approve and maintain the Approved Supplier Program.
	Conduct supplier qualifications, audits, and periodic reviews.
	Ensure proper raw material traceability and adherence to quality specifications.
	Investigate deviations, non-conformances, and customer complaints.
	Lead root cause analysis (RCA) and implement Corrective and Preventive Actions (CAPA).
	Manage change control for processes, materials, and equipment affecting product quality.
	Train staff on cGMP, SOPs, hygiene, and quality standards.
	Maintain training records and ensure ongoing competency of production and quality teams.
	Ensure proper documentation practices (GDP).
	Maintain and archive all quality records, batch documentation, and testing results per regulatory requirements.
	Monitor and ensure compliance with sanitation and cleaning validation protocols.

	Oversee environmental monitoring for microbial contamination (particularly for liquid products).
	Make final product disposition decisions (release, reject, or hold).
	Participate in product recall investigations and ensure recall procedures are in place.
	Identify process improvements to enhance product quality, efficiency, and compliance.
	Participate in cross-functional meetings to ensure quality considerations are integrated into production planning.</p>
					<p><strong>Skills</strong></p>
					<p>Gmp, fda, audit, cgmp</p>
					
					
					<p><strong>Additional Skills &amp; Qualifications</strong></p>
					<p>-	Knowledge of Excel, Word, and Adobe software.
-	Communication and management skills.
-	Ability to manage, carryout, and prioritize departmental functions.
-	Ability to see areas that need improvement and to address them.
-	Extensive <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">background</span></span></span></span></span></span> in quality systems and food and beverage manufacture.</p>
					<p><strong>Experience Level</strong></p>
					<p>Expert Level</p>

<p><strong>Description</strong></p><ul><li>Independently initiate, investigate, and complete Minor and low/medium severity Major deviations.</li><li>Collaboratively support high severity Major and Critical deviations under supervision.</li><li>Translate complex scientific events into clear, concise, and cohesive technical reports.</li><li>Conduct Root Cause Analysis (RCA), risk assessments, and impact evaluations on product quality (SISQP).</li><li>Identify and implement Corrective and Preventive Actions (CAPAs) to prevent recurrence.</li><li>Perform data gathering, trend analysis, cause mapping, and associate interviews.</li><li>Facilitate and participate in cross-functional meetings, alignment sessions, and deviation review boards.</li><li>Communicate investigation status and outcomes to internal teams and external clients through presentations and reports.</li><li>Work on the manufacturing floor to observe processes and collect data for investigations.</li><li>Manage multiple investigations and timelines, escalating issues as needed to ensure timely resolution.</li></ul><p><br></p><p><strong>Skills</strong></p><ul><li>Laboratory, Biology, Gmp, Quality control, Microbiology</li></ul><p><strong>Top Skills Details</strong></p><ul><li>Laboratory,Biology,Gmp</li></ul><p><strong>Additional Skills &amp; Qualifications</strong></p><ul><li>Bachelor’s degree in a scientific or technical discipline required.</li><li>3+ years of experience in a GMP-regulated environment, preferably in manufacturing or quality.</li><li>Strong technical writing skills with the ability to communicate complex topics to a broad audience.</li><li>Proficient in root cause analysis tools, risk assessment methodologies, and deviation management systems.</li><li>Experience with client-facing communication, including presentations and facilitated reviews.</li><li>Ability to manage multiple priorities in a fast-paced, cross-functional environment.</li></ul><p><br></p><p><br></p><p>Preferred Skills:</p><ul><li>Experience with TrackWise or similar quality management systems.</li><li>Strong facilitation and conflict resolution skills.</li><li>Familiarity with SISQP principles and regulatory compliance standards.</li><li>Positive, proactive, and adaptable mindset with a focus on continuous improvement.</li></ul><p><strong>Experience Level</strong></p><ul><li>Intermediate Level</li></ul>

Quality Records Investigtor

<h1 style="font-weight: 700;">Job Title: Quality Specialist</h1><br><h2>Job Description</h2><p>As the Quality Product Specialist, you will play a pivotal role in ensuring the integrity and highest level of quality for all products produced at our Franklin Park, IL plant. You will be responsible for inspecting work in process and finished products, ensuring compliance with quality standards, GMPs, and Food Safety guidelines.</p><br><h2>Responsibilities</h2><ul><li>Ensure inspection of the finished product output, guaranteeing that finished products meet quality specifications established by the Quality Department.</li><li>Examine quality reports prepared by production personnel and ensure the examination of monthly reports, requesting and verifying adjustments as required.</li><li>Conduct sensory sessions for semi-finished and finished products.</li><li>Support factory food allergen management program and maintain product coding.</li><li>Monitor and review information from materials, events, or the environment to detect or assess problems.</li><li>Train production employees on quality checks of the product, promoting self-control.</li><li>Record goods movements in SAP, including stock for quality controls and blocked stock.</li><li>Ensure all program requirements and standards regarding quality and food safety are implemented, practiced, and maintained.</li><li>Perform internal auditing, record statistical data, and analyze production data to verify compliance or determine deviations from existing standards.</li><li>Execute daily review of the Hazard Analysis Critical Control Point (HACCP) documentation.</li><li>Enforce and promote all company guidelines, policies, and good manufacturing practices.</li><li>Match or detect differences between colors, including shades of color and brightness; see details at close range; compare similarities and differences quickly and accurately; identify or detect patterns; add, subtract, multiply, or divide quickly and correctly.</li></ul><h2>Essential Skills</h2><ul><li>Quality inspection</li><li>Quality documentation</li><li>Audit</li><li>HAACP</li><li>Bachelor&#39;s Degree in Food Technology, Food Science, Biotechnology, or Food Chemistry</li><li>1-3 years of relevant work experience in food manufacturing</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Knowledge of raw materials, production processes, quality control, and other techniques for maximizing effective manufacturing and distribution of goods.</li><li>Quality assurance</li><li>Document control</li><li>Inspection</li></ul><h2>Work Environment</h2><p>This position is based in a fast-paced food manufacturing facility with hours from 9pm to 5am. The environment emphasizes efficiency and adherence to quality standards, requiring attention to detail and commitment to safety practices.</p><br>

Quality Specialist

<h1 style="font-weight: 700;">Job Title: Quality Specialist</h1><br><h2>Job Description</h2><p>Join our team as a Quality Specialist, where you will play a vital role in ensuring compliance with quality objectives and regulatory requirements within a dynamic and innovative environment.</p><br><h2>Responsibilities</h2><ul><li>Provide on-floor Quality Operations support for manufacturing, warehouse, and technical operations, including in-process checks and deviation identification.</li><li>Ensure all manufacturing activities comply with GMP and regulatory requirements.</li><li>Review and approve GMP documentation for accuracy and compliance.</li><li>Execute product-related activities, including apheresis material receipt and final product disposition.</li><li>Lead investigations into deviations, non-conformances, and process anomalies.</li><li>Review and approve deviations and CAPAs, ensuring compliant resolution.</li><li>Collaborate cross-functionally with Manufacturing, Quality Control, and Supply Chain teams.</li><li>Support continuous improvement initiatives to enhance quality and compliance.</li><li>Participate in internal audits and regulatory inspections.</li><li>Perform additional duties to support departmental goals.</li></ul><h2>Essential Skills</h2><ul><li>3+ years of cell therapy experience.</li><li>3-5 years of GMP manufacturing experience.</li><li>Quality Assurance oversight for manufacturing floors.</li><li>Experience with ISO 7 gowning.</li><li>Technical and growth mindset.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in a relevant scientific discipline.</li><li>5+ years of experience in the pharmaceutical or GMP industry.</li><li>Strong knowledge of batch record review, aseptic operations, and cGMP regulations.</li><li>Proficient in investigation tools like Fishbone diagrams, 5 Whys, and FMEA.</li><li>Ability to lead and close complex quality investigations.</li><li>Willingness to work in ISO 7 environments.</li><li>Flexibility to travel between facilities and work varying hours.</li></ul><h2>Work Environment</h2><p>Be part of a growing CDMO specializing in Cell/Gene Therapy at a brand-new site. The work environment involves engaging with innovative technologies and maintaining a commitment to operational excellence. Flexibility in working hours, including evenings and weekends, is required. Expect a collaborative atmosphere that encourages continuous learning and problem-solving.</p><br>

<h1 style="font-weight: 700;">Job Title: Quality Specialist - Validation</h1><br><h2>Job Description</h2><p>The Quality Specialist - Validation ensures adherence to current Good Manufacturing Practices (cGMP) and FDA Quality Systems throughout the evaluation, review, and approval of validation and quality assurance/control documentation. This role is essential in maintaining high-quality standards and compliance within the organization.</p><br><h2>Responsibilities</h2><ul><li>Assist in the development of cGMP operating procedures related to process, computer systems, and equipment validation.</li><li>Assure compliance with SOPs upon implementation and investigate additional corrective actions as needed.</li><li>Communicate with Field Quality/Operations and other personnel regarding Donor Center compliance and cGMP issues.</li><li>Ensure validation approaches align with regulatory expectations and industry standards.</li><li>Write and execute test cases to validate critical control points, user requirements, and functional designs.</li><li>Interact with Donor Center and Field Quality/Operations personnel to facilitate validation testing, ensuring timely and documented approval prior to routine use.</li><li>Analyze validation data to ensure acceptance criteria are met and assist in writing validation summaries.</li><li>Ensure milestones and timelines are met on assigned projects and prepare validation reports for distribution.</li><li>Evaluate adequacy of corrective actions and participate in the evaluation of processes, systems, and equipment needs.</li><li>Prepare validation equipment for use at the Donor Center and evaluate upon return.</li><li>Identify and determine actions for adding, removing, and/or revalidating processes, systems, and equipment.</li><li>Track and monitor process/system failures/events and provide feedback to Donor Center management.</li><li>Monitor and trend customer complaints and nonconformance related to equipment failures.</li></ul><h2>Essential Skills</h2><ul><li>Strong knowledge of current Good Manufacturing Practices (cGMPs) operating procedures and standard operating procedures.</li><li>Excellent quantitative and analytical skills.</li><li>Exceptional oral and written communication skills.</li><li>Strong critical thinking and problem-solving abilities.</li><li>Ability to identify errors and provide corrective action.</li><li>Proficient in Microsoft Office applications and computer applications used in the field.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree.</li></ul><h2>Work Environment</h2><p>The work is performed in both office and laboratory/manufacturing environments with exposure to biological fluids and potential infectious organisms. There is occasional exposure to extreme cold and high noise levels in production areas, as well as electrical office and laboratory equipment. Personal protective equipment, such as protective eyewear, garments, and gloves, is required. The role involves sitting for 4-6 hours daily, with occasional standing, bending, and twisting. Repetitive hand movements and precise coordinated finger movements are necessary. Lifting and carrying objects up to 50lbs may be required. Near and far vision correctable in one eye to 20/30 and to 20/100 in the other eye is essential. The ability to communicate complex information effectively and follow instructions is crucial.</p><br>

Quality Specialist - Validation

<h1><strong>Job Title: Quality Supervisor</strong></h1><p><br></p><h2>Job Description</h2><p>The Quality Supervisor provides leadership and support for the quality and operations teams during night shift operations. This role ensures compliance with regulatory, customer, and internal standards by supervising the night shift quality team, monitoring quality assurance processes, conducting audits and training, and supporting continuous improvement across packaging and sanitation operations. The Quality Supervisor acts as a key liaison between departments, ensuring that the night shift operates in alignment with food safety and quality expectations.</p><p><br></p><h2>Responsibilities</h2><ul><li>Supervise the night shift quality team, which includes 5 Quality Technicians and a Quality and Compliance Specialist.</li><li>Monitor quality assurance processes to ensure compliance with regulatory, customer, and internal standards.</li><li>Conduct audits and provide training to uphold quality standards.</li><li>Support continuous improvement across packaging and sanitation operations.</li><li>Act as a key liaison between departments to ensure alignment with food safety and quality expectations.</li></ul><h2>Essential Skills</h2><ul><li>Associates degree in the sciences or Bachelor&#39;s degree in the life sciences (Food Science, Microbiology, Biology or related field).</li><li>At least 2 years of experience in the food industry, with baking industry experience being most comparable.</li><li>Experience working under GMP, HACCP, and Food Safety principles.</li><li>Familiarity with SQF (GFSI).</li><li>Lead or supervisory experience.</li><li>Experience writing SOPs/procedures.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with metal detection/X-ray for troubleshooting is a plus.</li><li>Independent worker with the ability to spearhead projects and confidently implement changes.</li></ul>

Quality Supervisor

<h1><strong><u>Quality Systems Engineering Opportunity! </u></strong></h1><p><strong><em>For immediate consideration, please apply directly to this job posting AND email me at biacosta @actalentservices.comwith the following:</em></strong></p><p><strong>1) Word copy of resume</strong></p><p><strong>2) 2-3 professional references</strong></p><p><strong>3) 4-5 brief bullet points highlighting technical qualifications</strong></p><p><br></p><h2>Job Description</h2><p>We are seeking a highly experienced Level III Quality Systems Engineer to join our Quality and Regulatory team. This role is critical in ensuring the integrity and compliance of marketing claims associated with our medical devices. The ideal candidate will have a strong <span style="color: rgb(8, 7, 7); background-color: none;">background</span> in quality systems within the medical device industry and a proven ability to trace marketing claims to supporting engineering analyses and documentation. This individual will also be responsible for developing and maintaining SOPs related to the establishment and validation of marketing claims, with a focus on different user populations. Additionally, this role will involve collecting and reviewing existing documentation to identify and substantiate claims, and later, training key stakeholders on the newly developed claims process to ensure consistent understanding and implementation across the organization.</p><p><br></p><h2>Responsibilities</h2><ul><li>Collect and review existing internal documentation to identify potential marketing claims.</li><li>Organize and document findings to support traceability and validation efforts with internal project team.</li><li>Investigate and validate marketing claims by tracing them to engineering analyses, risk assessments, and supporting technical documentation.</li><li>Evaluate claims for accuracy, scientific validity, and compliance with regulatory standards.</li><li>Assess claims made for different user populations to ensure appropriate substantiation.</li><li>Utilize Pepper Flow software to manage and maintain traceability of claims to source documentation.</li><li>Ensure all documentation is audit-ready and compliant with internal and external quality standards.</li><li>Develop, implement, and maintain Standard Operating Procedures (SOPs) for the creation, review, and approval of marketing claims.</li><li>Collaborate with cross-functional teams (Marketing, R&amp;D, Regulatory, Clinical) to align SOPs with business and compliance needs.</li><li>Partner with Regulatory Affairs to ensure claims meet global regulatory requirements.</li><li>Work closely with Engineering and Clinical teams to gather and interpret data supporting claims.</li><li>Provide training and guidance to internal stakeholders on claim substantiation processes.</li><li>Design and deliver training sessions for key stakeholders on the new claims process.</li><li>Ensure consistent understanding and adoption of the process across relevant departments.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor’s degree in Engineering, Life Sciences, or related field (Master’s preferred).</li><li>8–10 years of experience in Quality Systems or Regulatory Affairs within the medical device industry.</li><li>Strong understanding of FDA regulations and other relevant standards.</li><li>Experience with Pepper Flow or similar document control/traceability systems.</li><li>Demonstrated ability to critically evaluate scientific and engineering data.</li><li>Excellent written and verbal communication skills.</li><li>Strong organizational and project management skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Familiarity with global regulatory environments (e.g., EU MDR, Health Canada).</li><li>Prior experience developing SOPs and quality documentation.</li><li>Knowledge of human factors and usability engineering as it relates to different user populations.</li></ul><h2>Work Environment</h2><p>This position is onsite in Irvine, CA. The role offers a dynamic work environment where collaboration with cross-functional teams is key. Benefits include 2 weeks PTO and 10 client-paid holidays</p>

Quality Systems Engineer

<h3>Now Hiring: Quality Systems Engineer</h3><p>Location : On-site in Irvine, CA |  Schedule: Mon–Wed + Every Other Friday</p><p><br></p><hr><h4>About the Role</h4><p>Are you ready to lead the charge in building a new Quality Management System (QMS) from the ground up? As a Quality Systems Engineer, you’ll play a pivotal role in shaping the future of our Neurovascular division. This is a high-impact opportunity to drive compliance, innovation, and operational excellence as we prepare for a major site qualification audit in early 2026. You’ll collaborate across departments to ensure our systems meet and exceed global regulatory standards—including ISO 13485:2016, FDA QSR/QMSR, and EU MDR—while supporting continuous improvement and certification readiness.</p><hr><h4>What You’ll Do</h4><ul><li>Lead the execution of quality plans and QMS implementation for a new site.</li><li>Partner with cross-functional teams to drive certification and compliance strategies.</li><li>Ensure audit readiness and provide expert support during regulatory inspections.</li><li>Support continuous improvement initiatives and system integration efforts.</li><li>Update Quality Manuals and Systems in alignment with evolving regulations.</li><li>Collaborate with R&amp;D, Regulatory Affairs, Supply Chain, Marketing, and more.</li></ul><hr><h4>What You Bring</h4><ul><li> 6+ years of experience in Quality Engineering, preferably in medical devices.</li><li> Proven success leading QMS build-outs and quality planning.</li><li> Expertise in FDA, ISO, and EU MDR regulations.</li><li> Proficiency with Windchill and ETQ systems.</li><li> Strong understanding of compliance, quality assurance, and regulatory affairs.</li><li> Bonus: Experience in neurovascular or high-risk medical device environments.</li></ul><hr><h4>Why Join Us?</h4><p>This is more than a job—it’s a chance to build something meaningful. You’ll be joining a team at a critical moment of transformation, with the autonomy to shape systems that ensure patient safety and product excellence. If you&#39;re passionate about quality, compliance, and making a difference in healthcare, we want to hear from you.</p>

<h1><strong><u>Quality Systems Engineering Opportunity! </u></strong></h1><p><strong><u>** For Immediate consideration please apply to this posting and email your resume to habels@actalentservices.com** </u></strong></p><p><br></p><h2>Job Description</h2><p>We are seeking a highly experienced Level III Quality Systems Engineer to join our Quality and Regulatory team. This role is critical in ensuring the integrity and compliance of marketing claims associated with our medical devices. The ideal candidate will have a strong <span style="color: rgb(8, 7, 7); background-color: none;">background</span> in quality systems within the medical device industry and a proven ability to trace marketing claims to supporting engineering analyses and documentation. This individual will also be responsible for developing and maintaining SOPs related to the establishment and validation of marketing claims, with a focus on different user populations. Additionally, this role will involve collecting and reviewing existing documentation to identify and substantiate claims, and later, training key stakeholders on the newly developed claims process to ensure consistent understanding and implementation across the organization.</p><p><br></p><h2>Responsibilities</h2><ul><li>Collect and review existing internal documentation to identify potential marketing claims.</li><li>Organize and document findings to support traceability and validation efforts with internal project team.</li><li>Investigate and validate marketing claims by tracing them to engineering analyses, risk assessments, and supporting technical documentation.</li><li>Evaluate claims for accuracy, scientific validity, and compliance with regulatory standards.</li><li>Assess claims made for different user populations to ensure appropriate substantiation.</li><li>Utilize Pepper Flow software to manage and maintain traceability of claims to source documentation.</li><li>Ensure all documentation is audit-ready and compliant with internal and external quality standards.</li><li>Develop, implement, and maintain Standard Operating Procedures (SOPs) for the creation, review, and approval of marketing claims.</li><li>Collaborate with cross-functional teams (Marketing, R&amp;D, Regulatory, Clinical) to align SOPs with business and compliance needs.</li><li>Partner with Regulatory Affairs to ensure claims meet global regulatory requirements.</li><li>Work closely with Engineering and Clinical teams to gather and interpret data supporting claims.</li><li>Provide training and guidance to internal stakeholders on claim substantiation processes.</li><li>Design and deliver training sessions for key stakeholders on the new claims process.</li><li>Ensure consistent understanding and adoption of the process across relevant departments.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor’s degree in Engineering, Life Sciences, or related field (Master’s preferred).</li><li>8–10 years of experience in Quality Systems or Regulatory Affairs within the medical device industry.</li><li>Strong understanding of FDA regulations and other relevant standards.</li><li>Experience with Pepper Flow or similar document control/traceability systems.</li><li>Demonstrated ability to critically evaluate scientific and engineering data.</li><li>Excellent written and verbal communication skills.</li><li>Strong organizational and project management skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Familiarity with global regulatory environments (e.g., EU MDR, Health Canada).</li><li>Prior experience developing SOPs and quality documentation.</li><li>Knowledge of human factors and usability engineering as it relates to different user populations.</li></ul><h2>Work Environment</h2><p>This position is onsite in Irvine, CA. The role offers a dynamic work environment where collaboration with cross-functional teams is key. Benefits include 2 weeks PTO and 10 client-paid holidays.</p>

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