<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>

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Quality Lab Technician

<h1 style="font-weight: 700;">Job Title: Quality Technician</h1><br><h2>Job Description</h2><p>We are seeking a dedicated Quality Technician to join our team. In this role, you will spend your day on the production floor performing quality checks, ensuring adherence to quality processes, and maintaining precise documentation. While the primary focus is on production, there is minimal lab work involved, primarily preparing samples for third-party testing. You will need to accurately interpret and follow reference documentation such as specifications and SOPs, comply with Good Manufacturing Practices (GMP&#39;s) and Good Laboratory Practices (GLP&#39;s), and communicate quality-related information effectively both verbally and in written form.</p><br><h2>Responsibilities</h2><ul><li>Perform quality checks on the production floor.</li><li>Ensure all quality processes are followed.</li><li>Maintain detailed and accurate documentation.</li><li>Prepare samples for third-party testing.</li><li>Interpret and follow specifications and SOPs accurately.</li><li>Comply with GMP&#39;s and GLP&#39;s.</li><li>Communicate quality-related information effectively.</li></ul><h2>Essential Skills</h2><ul><li>At least 8 months of quality control experience without a degree, or an associate degree in the sciences with no work experience.</li><li>Ability to conduct quality assurance and quality checks.</li><li>Strong communication skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Interest in a manufacturing/quality setting with opportunities for upward mobility.</li><li>Attention to detail and basic math skills.</li></ul><h2>Work Environment</h2><p>The position is on the first shift, from 7:00 AM to 3:30 PM, in a clean manufacturing environment. The facility is large with several production lines, requiring candidates to walk around and pull samples. This positive environment boasts a strong culture where employees are valued and trained for career development. The company manufactures a variety of products including shampoos, conditioners, and sunscreens.</p><br>

<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>

<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>

<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><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. 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 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>Quality Manager</strong></h1><p><br></p><h2>Job Description</h2><p>The Quality Manager will play a critical role in ensuring that all products meet safety, quality, and regulatory standards before they reach customers.</p><p><br></p><h2>Responsibilities</h2><ul><li>Develop, implement, and maintain quality assurance protocols and SOPs.</li><li>Supervise lab testing of finished products including alcolizer, pH, CO2, nitrogen, and carbonation.</li><li>Assist in obtaining SQF and GMP certifications.</li><li>Maintain documentation and traceability for all quality-related activities.</li><li>Manage and train QA Technicians.</li><li>Collaborate closely with the production team.</li><li>Address customer complaints and implement corrective actions.</li><li>Ensure co-packed products meet client specifications and expectations.</li><li>Source lab equipment and work with vendors.</li><li>Understand the blending process.</li><li>Implement Sensory panel testing for products.</li></ul><h2>Essential Skills</h2><ul><li>Quality assurance</li><li>Food safety</li><li>Food quality</li><li>Audit</li><li>SQF</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in Food Science, Microbiology, Chemistry, or related field</li><li>3+ years in QA/QC roles in the beverage or food industry</li></ul><h2>Work Environment</h2><p>The main facility is a brewery featuring a 2,200 sq ft warehouse with one production line and six 9,000-gallon tanks for blending. There is also a 4,400 sq ft packaging warehouse. The company is growing rapidly and is involved in packing products for established brands.</p>

<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>

Quality Operations Manager

<h1 style="font-weight: 700;">Job Title: Quality Operations Manager</h1><br><h2>Job Description</h2><p>As a Quality Operations Manager, you will ensure facility compliance with cGMP regulations, oversee the Quality Management System, manage regulatory inspections, and stay updated on relevant regulatory changes. You will be responsible for maintaining high standards in quality management and regulatory compliance across all operations.</p><br><h2>Responsibilities</h2><ul><li>Ensure facility compliance with cGMP regulations for dietary supplements, OTC drugs, and skin care.</li><li>Maintain and oversee the Quality Management System, including SOPs, work instructions, and quality manuals.</li><li>Manage regulatory inspections and coordinate responses to findings.</li><li>Stay updated on relevant regulatory changes and ensure facility compliance.</li><li>Review and approve Master Manufacturing Records and Batch Production Records for accuracy and compliance.</li><li>Oversee and approve in-process checks such as pH, viscosity, microbial limits, and fill weights.</li><li>Ensure proper execution of line clearance and changeover procedures.</li><li>Supervise incoming raw material testing for identity, potency, microbiological content, and heavy metals.</li><li>Oversee finished product testing to ensure products meet specifications.</li><li>Review and approve Certificates of Analysis from third-party labs.</li><li>Approve and maintain the Approved Supplier Program, conducting supplier qualifications, audits, and periodic reviews.</li><li>Ensure proper raw material traceability and adherence to quality specifications.</li><li>Investigate deviations, non-conformances, and customer complaints.</li><li>Lead root cause analysis and implement Corrective and Preventive Actions.</li><li>Manage change control for processes, materials, and equipment affecting product quality.</li><li>Train staff on cGMP, SOPs, hygiene, and quality standards, maintaining training records.</li><li>Ensure proper documentation practices and archive all quality records per regulatory requirements.</li><li>Monitor and ensure compliance with sanitation and cleaning validation protocols.</li><li>Oversee environmental monitoring for microbial contamination, particularly for liquid products.</li><li>Make final product disposition decisions, including release, reject, or hold.</li><li>Participate in product recall investigations and ensure recall procedures are in place.</li><li>Identify process improvements to enhance product quality, efficiency, and compliance.</li><li>Participate in cross-functional meetings to integrate quality considerations into production planning.</li></ul><h2>Essential Skills</h2><ul><li>Operations management experience leading both Quality Assurance and Quality Control departments.</li><li>10 years of experience in quality operations within the food and beverage sector.</li><li>5 years of management experience in the quality operations of the food and beverage sector, preferably dietary supplements.</li><li>4-Year degree in Food Science or equivalent field.</li><li>Excellent communication and management skills.</li><li>Ability to manage, carry out, and prioritize departmental functions.</li><li>Extensive <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">background</span></span> in quality systems and food and beverage manufacture.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Knowledge of Excel, Word, and Adobe software.</li><li>Driven, organized, and detail-oriented individual.</li><li>Ability to see areas that need improvement and address them.</li></ul><h2>Work Environment</h2><p>This role encompasses facility-wide operations, including warehousing, shipping, receiving, manufacturing, packaging, and QC labs, ensuring a comprehensive approach to quality management.</p><br>

<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 - 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>Quality Specialist - Validation</strong></h1><p><br></p><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><p><br></p><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>

<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

<h2>Responsibilities</h2><ul><li>Support IATF auditing by leading internal and external audits and ensuring audit readiness.</li><li>Develop and maintain quality documentation including control plans, PFMEAs, process flows, and inspection instructions.</li><li>Coordinate and execute APQP and PPAP activities for new product launches and annual re-validations.</li><li>Manage document control systems and calibration programs for gages and equipment.</li><li>Lead root cause analysis and corrective action processes (8D, 5-Why, Fishbone) for internal and customer quality issues.</li><li>Support layered audits and manage corrective actions stemming from audit findings.</li></ul><h2>Essential Skills</h2><ul><li>Associate or Bachelor’s degree in Engineering, Quality, or a related field; equivalent experience considered.</li><li>2–5 years of experience in quality systems engineering.</li><li>Strong knowledge of IATF, ISO 9001, and related quality standards.</li><li>Experience in audit scheduling, execution, and follow-up.</li><li>Proficiency in quality tools such as SPC, MSA, GD&amp;T, and CMM programming.</li></ul>

<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>

<h1 style="font-weight: 700;">Job Title: Quality Systems Engineer</h1><br><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><br><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 the 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 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>Strong <span style="color: rgb(8, 7, 7); background-color: none;">background</span> in quality systems within the medical device industry.</li><li>Ability to trace marketing claims to supporting engineering analyses and documentation.</li><li>Understanding of FDA regulations and other relevant standards.</li><li>Experience with Pepper Flow or similar document control/traceability systems.</li><li>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>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>Familiarity with global regulatory environments.</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 based onsite in Irvine, CA. Employees enjoy two weeks of paid time off and ten client-paid holidays.</p><br>

<h1 style="font-weight: 700;">Job Title: Quality Systems Specialist</h1><br><h2>Job Description</h2><p>The Quality Systems Specialist is responsible for providing support and continuous improvement to the Quality System. The role involves ensuring compliance with internal audits, GMP standards, regulatory and customer requirements, sanitation, pest control, nonconformance investigations, CAPA, customer complaints, change control, and managing HACCP &amp; PCQI certifications. The position requires excellent verbal and written communication skills to compile and present data and trends for Quarterly Management Review, Annual Product Review, and Annual Management Review.</p><br><h2>Responsibilities</h2><ul><li>Manage regulatory inspections, customer, and third-party audits by presenting documents and answering auditor’s questions.</li><li>Schedule and coordinate audits, acting as the point of contact.</li><li>Ensure corrective actions are completed and respond to audit findings.</li><li>Maintain audit files and manage GMP audit programs at the manufacturing site and WI warehouses.</li><li>Represent Quality in QA/Ops Gemba audits and schedule audits with area leaders.</li><li>Photograph and report findings, and assign Audit Work Orders as needed.</li><li>Manage CAPA programs, ensuring CAPAs are effective and closed timely.</li><li>Oversee site QAM initiatives and manage HACCP and Food Safety programs, ensuring compliance with food safety requirements.</li><li>Interact with customers and customer portals for audits, corrective actions, and customer satisfaction.</li><li>Manage Internal Audit programs and present quarterly Internal Audit Reports.</li><li>Coordinate with Production and other departments to discuss, resolve, and eliminate documentation observations.</li><li>Provide guidance to Document Coordinators to process Procedures and Work Instructions.</li><li>Identify, lead or manage quality system document improvements focusing on effectiveness, efficiency, and simplification.</li><li>Drive continuous improvement initiatives as site representative for Docushare, Agile, and other systems.</li><li>Plan, prioritize, and work under pressure to meet deadlines with good follow-up and documentation skills.</li><li>Organize, direct, and manage teams in a problem-solving environment.</li><li>Determine severity of quality issues with QA/QS Manager and properly interpret regulatory standards.</li><li>Maintain open communication with all departments to assist with arising issues.</li></ul><h2>Essential Skills</h2><ul><li>Expertise in quality systems and quality assurance.</li><li>Experience in pharmaceutical and medical device industries.</li><li>Proficiency in GMP and cGMP standards.</li><li>Knowledge of 21 CFR 820, ISO, and BRC standards.</li><li>Ability to work with DocuShare, Documentum, and secured documents.</li><li>Skill in using pivot tables and audit trails.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in the Sciences.</li><li>Five years of GMP, cGMP experience within food manufacturing.</li><li>Three years of experience with food safety audits.</li><li>PCQI Certification is a plus.</li></ul><h2>Work Environment</h2><p>The role is based in an office within a wet wipe (OTC and Med Device) and coffee filter manufacturing facility.</p><br>

Quality Systems Specialist

<h1 style="font-weight: 700;">Job Title: Quality Technician</h1><br><h2>Job Description</h2><p>We are seeking a skilled Quality Technician to join our team. The role involves ensuring the highest standards of quality and reliability in our production processes, and you will play a key part in maintaining our commitment to excellence.</p><br><h2>Responsibilities</h2><ul><li>Review and approve engineering packets for new orders as part of a cross-functional review.</li><li>Develop Process Control Plans and PFMEA’s, as required.</li><li>Interact with external customers and suppliers regarding product nonconformances and conduct failure analysis, when necessary.</li><li>Initiate internal and external Corrective Actions (CAR’s/SCAR’s) as needed.</li><li>Supervise incoming and first article inspection areas and generate customer PPAP reports.</li><li>Determine sampling plans, and create forms and instructions for recording, evaluating, and reporting quality and reliability trend data.</li><li>Maintain the Calibration program, ensure tooling and equipment are scheduled for calibration at defined intervals, and maintain calibration records.</li><li>Manage Quality and Inspection Team to meet customer expectations.</li><li>Perform additional duties as assigned.</li></ul><h2>Essential Skills</h2><ul><li>Experience in inspection and quality control.</li><li>Ability to improve processes and ensure quality assurance.</li><li>Knowledge of Quality Engineering and Quality Technician processes.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Ability to manage quality on the production floor and in products.</li></ul><h2>Work Environment</h2><p>This position is located in the quality engineering department. You will be part of a smaller company that values teamwork and collaboration. The role requires working closely with a team member who has been with the company for three years, ensuring a supportive and knowledgeable work environment.</p><br>

Quality Technician

<h1 style="font-weight: 700;">Job Title: Quality Technician</h1><br><h2>Job Description</h2><p>We are seeking a Quality Technician to perform quality checks on medical-grade plastics, rubbers, silicones, and similar materials. The role involves documenting all quality checks, quality data, and product information. The technician will work closely with production personnel to ensure quality standards are met and will ensure clean rooms are maintained, sterile practices are adhered to, and products are made in compliance with FDA regulations.</p><br><h2>Responsibilities</h2><ul><li>Perform quality checks on medical-grade materials such as plastics, rubbers, and silicones.</li><li>Document all quality checks, quality data, and product information.</li><li>Collaborate with production personnel to ensure quality standards are met.</li><li>Maintain clean rooms and adhere to sterile practices.</li><li>Ensure products are manufactured following FDA regulations.</li></ul><h2>Essential Skills</h2><ul><li>Experience in quality control, particularly in medical device products.</li><li>Proficiency in performing visual inspections and measurements.</li><li>Ability to document quality processes effectively.</li><li>Knowledge of quality assurance practices.</li><li>Understanding of sterilization processes and clean room protocols.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with medical devices.</li><li>Familiarity with materials like plastics, rubbers, and silicones.</li></ul><h2>Work Environment</h2><p>The position is based in a medical device clean room environment, known for its high cleanliness standards. It is a 3rd shift role with hours from Monday through Friday, 3 pm to 11 pm, and involves working with about 25 other team members on the shift. Candidates may initially train on 1st shift but will likely start on 2nd shift. The facility requires business casual attire, including jeans, a plain shirt, and work boots. The role offers a 2nd shift premium of $1.25/hr.</p><br>

<p><strong>Description</strong></p><p>- Perform dimensional and visual inspections on critical medical device components or assemblies using various measurement tools like calipers, micrometers, vision inspection equipment, gauges, etc.</p><p>- Conduct functional tests and verify conformance to detailed specifications and tolerances</p><p>- Interpret engineering drawings, specifications, and work instructions</p><p>- Record and maintain accurate inspection data, including lot history and traceability records</p><p>- Support lot release, material review, and root cause analysis for nonconforming parts</p><p>- Participate in audits and provide complete, well-organized inspection documentation</p><p>- Assist in implementing corrective actions and reinforcing compliance with ISO 13485 and FDA regulations</p><p>- Ensuring adherence to GDP (Good Documentation Practices) and GMP (Good Manufacturing Practices) requirements</p><p>- Nonconformance, CAPA, and Material Review Board Support</p><p><br></p><p><strong>Additional Skills &amp; Qualifications</strong></p><p>- Minimum 3–5 years of quality technical experience in the medical device industry required.</p><p>- Proven experience inspecting critical or high-precision components and/or devices.</p><p>- Familiarity with ISO 13485, and Good Documentation Practices (GDP).</p><p>- Proficiency with inspection equipment and interpreting engineering drawings and GD&amp;T.</p><p>- Experience using Excel, electronic QMS platforms (e.g., Minitab, ETQ, Master Control), and document control systems.</p><p>- Excellent attention to detail, organization, and communication skills.</p><p><br></p><p><strong>Preferred Qualifications:</strong></p><p>- CQI or CQT certification</p><p>- Experience with cleanroom manufacturing in a medical device setting.</p><p>- Working knowledge of SPC and data analysis tools such as Minitab.</p><p>- Familiarity with Failure Investigation techniques.</p>

<h1><strong>Quality Technician</strong></h1><p><br></p><h2>Job Description</h2><p>This position offers an exciting opportunity to work onsite in Nashville, Tennessee, as a Quality Technician within a vibrant production environment. You will be responsible for visually inspecting and removing defective products to ensure quality standards are maintained.</p><p><br></p><h2>Responsibilities</h2><ul><li>Follow instructions and adhere to all safety protocols.</li><li>Visually identify and remove defective products from the production line.</li><li>Maintain attentiveness throughout the duration of production shifts.</li><li>Be flexible and available for overtime to accommodate changes in production schedules.</li><li>Collaborate effectively with other employees to maintain a harmonious work environment.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in inspection and quality checking processes.</li><li>Ability to identify product defects accurately.</li><li>Strong attention to detail during production shifts.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>6 months to 1 year of experience in Quality roles, preferably within Food and Beverage manufacturing.</li><li>High School Diploma is required.</li></ul><h2><br></h2>

<h1><strong>Job Title: Construction Quality Control Technician</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a detail-oriented and proactive Quality Technician to support our construction projects by ensuring compliance with quality standards and regulatory requirements. This role is critical in maintaining the integrity of our work through audits, inspections, documentation, and reporting.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct regular audits and inspections on construction sites to ensure adherence to project specifications, codes, and safety standards.</li><li>Perform specification checks on materials and workmanship to verify compliance with engineering drawings and client requirements.</li><li>Maintain accurate and timely documentation of inspection results, non-conformance reports, and corrective actions.</li><li>Prepare and submit quality reports to project managers and stakeholders.</li><li>Collaborate with project teams to resolve quality issues and implement continuous improvement initiatives.</li><li>Support internal and external audits, including client and regulatory inspections.</li><li>Ensure all quality control procedures are followed throughout the project lifecycle.</li></ul><h2>Essential Skills</h2><ul><li>Construction management</li><li>Quality assurance</li><li>Construction</li><li>Audit</li><li>Inspection</li><li>General contractor</li><li>Project coordination</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High school diploma or equivalent required; associate degree or technical certification in construction, engineering, or quality management preferred.</li><li>2+ years of experience in a quality control or quality assurance role, preferably within a construction or EPCM environment.</li><li>Strong understanding of construction processes, materials, and quality standards.</li><li>Familiarity with ISO standards and QA/QC documentation practices.</li><li>Excellent attention to detail, organizational, and communication skills.</li><li>Proficiency in Microsoft Office and quality management software.</li><li>Experience with root cause analysis and corrective/preventive action (CAPA) processes.</li><li>Knowledge of industry-specific regulations and standards (e.g., ASTM, OSHA).</li><li>Ability to read and interpret technical drawings and specifications.</li></ul><h2>Work Environment</h2><p>On-site at large pharma project in Sanford.</p>

<h1 style="text-align: center;"><strong>1st Shift Quality Technician</strong></h1><p><br></p><h2>Job Description</h2><p>The Quality Technician plays a vital role in performance management by analyzing data, identifying opportunities for improvement, and driving actions for supplier development. This position is responsible for proactively reducing and preventing defects in supplied materials, leading cross-functional teams to enhance performance, and mitigating quality risks. The role includes submitting and reviewing supplier corrective action requests, leading on-site supplier engagements, and developing innovative solutions to complex problems.</p><p><br></p><h2>Responsibilities</h2><ul><li>Analyze performance data to identify opportunities for improvement and drive supplier development actions.</li><li>Reduce and prevent defects in supplied materials and verify defect claims.</li><li>Lead cross-functional teams to pursue performance improvements aligned with organizational goals.</li><li>Mitigate business impact from supplied material defects and manage supplier quality risks.</li><li>Submit, review, coach, and accept supplier corrective action requests.</li><li>Lead on-site supplier engagements, including performance reviews, process walks, and Quality System audits.</li><li>Develop solutions to complex problems requiring ingenuity, creativity, and innovation.</li><li>Provide project management guidance and support to projects and processes.</li><li>Exercise independent judgment using methods, techniques, and evaluation criteria for obtaining results.</li><li>Lead within supplied material performance organizational strategies and enhance Supplier Quality standard work.</li><li>Influence supplier selection and facilitate cross-functional teams in failure analysis and RCCA investigations.</li><li>Support development and maintenance of work instructions, test instructions, and audit processes.</li><li>Develop and maintain inspection instructions and equipment to meet technical data package requirements.</li></ul><h2>Essential Skills</h2><ul><li>Quality control and inspection</li><li>Data entry and admin support</li><li>Quality assurance and visual inspection</li><li>Use of calipers and inspection equipment</li><li>Root cause analysis and data analysis</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>University Degree with minimum 2 years of relevant experience or Advanced Degree in a related field</li><li>In absence of a degree, 6 years of relevant experience</li><li>Experience in Supplier Management with manufactured products</li><li>Experience with Quality Management Systems (QMS) and Continuous Improvement</li><li>Experience with data analysis, specification review, and inspection methods</li><li>Project management and team facilitation skills</li></ul><h2>Work Environment</h2><p>This position is fully on-site, offering an opportunity to earn a full-time permanent position within a well-known and growing company. Monday - Friday 7AM-3:30PM </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>

<h2><strong>Key Responsibilities and Duties</strong></h2><p>• Review records for product release and documents for completeness &amp; accuracy under a production schedule</p><p>• Review and update (as authorized) quality system documentation</p><p>• Log, file, maintain and archive various QA reports &amp; records</p><p>• Track key performance metrics</p><p>• Prepares and collects materials for the monthly Instrument &amp; Reagent Quality Review meetings</p><p>• Investigates and works with other departments to resolve quality issues related to area assigned</p><p>• Participates in internal compliance audits to established Quality System Manual and applicable regulations and standards</p><p>• Participates in continuous improvement efforts by completing corrective/preventive actions as assigned</p><p>• Assist other Quality Assurance personnel in Material Review Board (MRB) activities as needed</p><h2><strong>Essential Skills</strong></h2><ul><li>Proficiency in quality assurance and documentation review.</li><li>Strong attention to detail.</li><li>Experience in a Good Manufacturing Practices (GMP) environment.</li><li>Experience participating in formal audits.</li></ul>

<h1><strong>Quality Technician</strong></h1><p><strong><u>Responsibilities </u></strong></p><ul><li>Verify line clearance prior to startup.</li><li>Perform equipment swabbing after sanitation.</li><li>Conduct quality audits for each production line throughout the shift.</li><li>Document in-line process check results per pre-approved specifications.</li><li>Report any out-of-specification or non-conformance issues.</li><li>Ensure immediate corrective action is completed before startup for non-conformance.</li><li>Label and store non-compliant products following MRB process.</li><li>Conduct periodic quality and GMP audits of the production area.</li><li>Audit ingredients staged for manufacturing to ensure no expired materials are used.</li><li>Perform temperature audits of ingredients, WIP, and finished products.</li><li>Prepare shift report for next shift follow-up.</li><li>Conduct case count audits on all products.</li><li>Perform daily pre-operational inspections.</li><li>Assist in metal detector validations and line checks.</li><li>Ensure operators follow metal detector SOP.</li><li>Report any food safety risks to the supervisor.</li><li>Collect samples from raw materials, in-process, and finished products for lab testing.</li></ul><p><strong><u>Qualifications </u></strong></p><ul><li>1 year of experience in food manufacturing quality.</li><li>Demonstrated GMP experience.</li><li>Ability to work cross-functionally with other departments and in a team setting. </li><li>Ability to work in a fast paced environment. </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><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>

<p><strong>Description</strong></p><p>- Perform dimensional and visual inspections on critical medical device components or assemblies using various measurement tools like calipers, micrometers, vision inspection equipment, gauges, etc.</p><p>- Conduct functional tests and verify conformance to detailed specifications and tolerances</p><p>- Interpret engineering drawings, specifications, and work instructions</p><p>- Record and maintain accurate inspection data, including lot history and traceability records</p><p>- Support lot release, material review, and root cause analysis for nonconforming parts</p><p>- Participate in audits and provide complete, well-organized inspection documentation</p><p>- Assist in implementing corrective actions and reinforcing compliance with ISO 13485 and FDA regulations</p><p>- Ensuring adherence to GDP (Good Documentation Practices) and GMP (Good Manufacturing Practices) requirements</p><p>- Nonconformance, CAPA, and Material Review Board Support</p><p><br></p><p><strong>Additional Skills &amp; Qualifications</strong></p><p>- Minimum 3–5 years of quality technical experience in the medical device industry required.</p><p>- Proven experience inspecting critical or high-precision components and/or devices.</p><p>- Familiarity with ISO 13485, and Good Documentation Practices (GDP).</p><p>- Proficiency with inspection equipment and interpreting engineering drawings and GD&amp;T.</p><p>- Experience using Excel, electronic QMS platforms (e.g., Minitab, ETQ, Master Control), and document control systems.</p><p>- Excellent attention to detail, organization, and communication skills.</p><p><br></p><p><strong>Preferred Qualifications:</strong></p><p>- CQI or CQT certification</p><p>- Experience with cleanroom manufacturing in a medical device setting.</p><p>- Working knowledge of SPC and data analysis tools such as Minitab.</p><p>- Familiarity with Failure Investigation techniques.</p><p><br></p><p><br></p><p><br></p>

<h1 style="font-weight: 700;">Job Title: Quality Technician</h1><br><h2>Job Description</h2><p>Establish and implement procedures for maintaining high standards of quality, reliability, and safety of products, raw materials, and services at assigned locations. Perform random quality audits on the production floor to verify processes are followed and customer specifications are met. Provide support in creating standard operating procedures (SOPs) and other supporting documents. Coordinate and administer third-party quality audits, schedules, communication, reports, and tracking of follow-up actions. Coordinate and perform internal quality system audits at the assigned location. Administer the corrective/preventive action program, including tracking the status of open actions, receiving and reviewing responses, and disposition of material in a timely manner. Complete customer quality documentation, including First Article Documents, Control Plans, FMEA’s, PPAP’s, and Capability Studies.</p><br><h2>Responsibilities</h2><ul><li>Establish and implement procedures for maintaining quality standards.</li><li>Perform random quality audits on the production floor.</li><li>Support in creating standard operating procedures (SOPs).</li><li>Coordinate and administer third-party quality audits.</li><li>Perform internal quality system audits at assigned locations.</li><li>Administer corrective/preventive action programs.</li><li>Complete customer quality documentation.</li></ul><h2>Essential Skills</h2><ul><li>Inspection</li><li>Quality control</li><li>Quality assurance</li><li>Calipers</li><li>Blueprint reading</li><li>Micrometer usage</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Minimum of 5 years of industrial manufacturing and/or quality control experience.</li><li>Experience with lean quality concepts and initiatives such as Continuous Improvement and The 5 Why’s.</li><li>Auditing experience.</li><li>Degree in quality engineering or related field preferred.</li><li>Equivalent combination of education and experience may substitute for the degree.</li></ul><h2>Work Environment</h2><p>Work is conducted Monday through Friday from 8:00 am to 4:30 pm. Overtime may be required to support business needs.</p><br>

<p><strong>Description</strong></p><p>- Perform dimensional and visual inspections on critical medical device components or assemblies using various measurement tools like calipers, micrometers, vision inspection equipment, gauges, etc.</p><p>- Conduct functional tests and verify conformance to detailed specifications and tolerances</p><p>- Interpret engineering drawings, specifications, and work instructions</p><p>- Record and maintain accurate inspection data, including lot history and traceability records</p><p>- Support lot release, material review, and root cause analysis for nonconforming parts</p><p>- Participate in audits and provide complete, well-organized inspection documentation</p><p>- Assist in implementing corrective actions and reinforcing compliance with ISO 13485 and FDA regulations</p><p>- Ensuring adherence to GDP (Good Documentation Practices) and GMP (Good Manufacturing Practices) requirements</p><p>- Nonconformance, CAPA, and Material Review Board Support</p><p><br></p><p><strong>Additional Skills &amp; Qualifications</strong></p><p>- Minimum 3–5 years of quality technical experience in the medical device industry required.</p><p>- Proven experience inspecting critical or high-precision components and/or devices.</p><p>- Familiarity with ISO 13485, and Good Documentation Practices (GDP).</p><p>- Proficiency with inspection equipment and interpreting engineering drawings and GD&amp;T.</p><p>- Experience using Excel, electronic QMS platforms (e.g., Minitab, ETQ, Master Control), and document control systems.</p><p>- Excellent attention to detail, organization, and communication skills.</p><p><br></p><p>Preferred Qualifications:</p><p><br></p><p>- CQI or CQT certification</p><p>- Experience with cleanroom manufacturing in a medical device setting.</p><p>- Working knowledge of SPC and data analysis tools such as Minitab.</p><p>- Familiarity with Failure Investigation techniques.</p><p><br></p>

<h1><strong>Quality Technician</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a dedicated Technician to perform daily evaluations and approvals of finished products, process quality checks, and routine product testing. This role requires responsible operating equipment calibration, troubleshooting, and documentation. The Technician will conduct ingredient inspections, packaging inspections, inventory control, and maintain sample archives. Accurate recording of test results and effective communication with operating departments and management are crucial. The role also involves performing in-process quality checks, collecting test samples, troubleshooting equipment, and performing mechanical maintenance. A commitment to maintaining a clean and safe laboratory environment is essential.</p><p><br></p><h2>Responsibilities</h2><ul><li>Perform daily evaluation and approval of finished products and process quality checks.</li><li>Conduct basic microbiological testing.</li><li>Calibrate equipment, troubleshoot issues, and calculate dilutions.</li><li>Inspect ingredients and packaging, manage inventory, and maintain sample archives.</li><li>Conduct laboratory tests including solvent extraction, sieving, pH etc.</li><li>Test raw ingredients and finished packaged products.</li><li>Record test results and communicate with operating departments and management.</li><li>Perform in-process quality checks and collect test samples.</li><li>Troubleshoot equipment and perform mechanical maintenance.</li><li>Maintain a clean and safe laboratory work environment.</li></ul><h2>Essential Skills</h2><ul><li>0-2 years of production experience.</li><li><span style="color: rgb(8, 7, 7); background-color: none;">Background</span> in food manufacturing.</li></ul>

<h1><strong>Job Title: Quality Technician</strong></h1><p><br></p><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><p><br></p><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 in a food manufacturing environment. 2 schedules, 1st and 3rd shift openings. 6am - 2pm and 10pm to 6am respectively.</p>

<h1><strong>(August - November)</strong></h1><p><br></p><h2>Job Description</h2><p>The technician will be responsible for pulling samples from trucks and checking for moisture content. You will operate the scale and maintain excellent customer service with external customers and grain haulers. Proficiency with computer systems and applications is required, as is the ability to grade corn based on training provided. You will also assist other personnel as needed and complete tasks promptly as assigned by the Manager, while maintaining a team environment with other departments.</p><p><br></p><h2>Responsibilities</h2><ul><li>Pull samples from trucks and check for moisture.</li><li>Operate scale and maintain customer service with external customers and grain haulers.</li><li>Operate computer system and become proficient with applications.</li><li>Grade corn based on training by Manager.</li><li>Assist other personnel as needed.</li><li>Complete tasks accurately and in a timely manner as assigned by Manager.</li><li>Maintain a team environment with other departments.</li><li>Ensure high levels of customer service and maintain a friendly atmosphere.</li><li>Adhere to company guidelines, regulatory standards, product quality, food safety, employee and environmental standards.</li><li>Read and interpret Material Safety Data Sheets (MSDS) and comply with safe use or personal protective equipment requirements.</li><li>Maintain a clean and organized work area, ensuring serviceability and accountability of tools, equipment, and supplies.</li><li>Learn and understand basic operation of facilities process to better understand company needs.</li><li>Notify the Manager or appropriate management member of any inventory discrepancies.</li><li>Perform other duties as assigned.</li></ul><h2>Essential Skills</h2><ul><li>Sample preparation and testing.</li><li>Quality inspection.</li><li>Leadership and communication.</li><li>Innovation and conflict management.</li><li>Problem-solving and being a self-starter.</li><li>Computer technology proficiency.</li><li>Moisture testing and customer service.</li><li>Ability to work independently.</li><li>Experience with MS Word, Excel, Outlook.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High school diploma or equivalent required.</li><li>2 years of previous food manufacturing experience preferred.</li><li>Excellent communication skills.</li><li>Ability to work flexible hours when needed.</li></ul><h2>Work Environment</h2><p>The role involves grading, probing, and running grain lab tests on incoming trucks. This is a seasonal support position for the harvesting season, running from August to November, with work hours from Monday to Friday, 7 AM to 3 PM. </p>

Quality Technician - Seasonal

<h1 style="text-align: center;"><strong>Quality Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>The Process/Manufacturing/Quality Engineer will be responsible for ensuring that all manufacturing processes meet the stringent quality standards required for Class III medical devices. This role involves developing, implementing, and maintaining quality systems and processes to ensure compliance with regulatory requirements and industry standards. The main focus will be reporting directly with the OEM and solely reporting to their HQ&#39;s leadership team on the quality assurance that is mandated.</p><p><br></p><h2>Responsibilities</h2><ul><li>Develop and implement process validation protocols and reports (IQ, OQ, PQ) to ensure manufacturing processes are capable and compliant.</li><li>Conduct root cause analysis and implement corrective and preventive actions (CAPA) to address process-related quality issues.</li><li>Collaborate with cross-functional teams, including R&amp;D, Manufacturing, and Regulatory Affairs, to ensure product quality and compliance.</li><li>Monitor and analyze process performance data to identify trends and areas for improvement.</li><li>Lead process improvement initiatives to enhance product quality, reduce waste, and increase efficiency.</li><li>Ensure compliance with FDA regulations and other applicable standards.</li><li>Participate in internal and external audits, providing necessary documentation and support.</li><li>Train and mentor production staff on quality standards and best practices.</li></ul><h2>Essential Skills</h2><ul><li>Process Improvement</li><li>Manufacturing process</li><li>Continuous Improvement</li><li>Lean manufacturing</li><li>Six Sigma</li><li>Process engineering</li><li>Manufacturing engineering</li><li>Quality engineering</li><li>Validation</li><li>Quality assurance</li><li>Quality improvement</li><li>Quality management system</li><li>Manufacturing quality</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in Mechanical, Manufacturing, Bio, Industrial Engineering, or a related field.</li><li>Minimum of 5 years of experience in manufacturing engineering, preferably in the medical device industry (high volume manufacturing).</li><li>Lean Six Sigma certification is highly desirable.</li><li>High quality documentation standards knowledge.</li><li>Hands-on floor work ability.</li></ul>

Quality/manufacturing Engineer

<h1><strong>Job Title: Manufacturing Quoting Specialist </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>The Quoting Specialist will be responsible for developing, maintaining, and reporting on all quoting metrics. The role involves creating quotes for both new and existing projects and products, updating prices on existing production items, and implementing cost-saving initiatives. The specialist will also develop new and improve existing quoting and costing practices.</p><p><br></p><h2>Responsibilities</h2><ul><li>Maintain all aspects and data related to quotes in process and the quotes log.</li><li>Assist the Director of Sales and Marketing with quote follow-up, tracking, and filing.</li><li>Collaborate with purchasing to secure material quotes at various levels above and below current purchase quantities.</li><li>Contact new and existing outside vendors for new part quotes, including metals, resin, concentrate, ink, labels, and inserts.</li><li>Train associates in quoting processes and the information required for successful quoting.</li><li>Implement lean strategies to evaluate and streamline quoting operations.</li><li>Support Project Managers in tasks related to new product validations and launches.</li><li>Manage and lead projects with direct customer contact.</li><li>Assist in the development and implementation of continuous improvements in molding, tooling, printing, and other manufacturing operations.</li><li>Develop and manage project plans and activities to drive improvements.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in quoting, ERP systems, and sales order entry.</li><li>Experience in engineering administration and project management.</li><li>Strong skills in customer service and data entry.</li><li>Understanding of a manufacturing environment.</li><li>Proficiency in math, pricing, and SolidWorks.</li><li>Associates Degree in Engineering or Business Degree.</li><li>2+ years experience in costing, quoting, and manufacturing.</li><li>2+ years experience with Excel tables, formula writing, and mathematics.</li><li>Knowledge of ERP systems, especially IQMS, and IT applications.</li><li>Project management skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>SOLIDWORKS proficiency desired.</li><li>Knowledge of plastic injection molding processes is a plus.</li><li>Proficiency in Microsoft Office (Excel, Word, PowerPoint, Outlook, Project).</li><li>Spanish speaking, reading, and writing bilingual ability is a plus.</li></ul><h2>Work Environment</h2><p>This role is set in a large company environment, offering opportunities for growth and experience. The workplace supports a manufacturing setting with a focus on engineering and business processes. The position requires proficiency in various IT applications and an understanding of lean manufacturing principles.</p>

Quoting Specialist

<h1 style="text-align: center;"><strong>Job Title: Quoting Specialist</strong></h1><p><br></p><h2>Job Description</h2><p>The Quoting Specialist will be responsible for developing, maintaining, and reporting on all quoting metrics. The role involves creating quotes for both new and existing projects and products, updating prices on existing production items, and implementing cost-saving initiatives. The specialist will also develop new and improve existing quoting and costing practices.</p><p><br></p><h2>Responsibilities</h2><ul><li>Maintain all aspects and data related to quotes in process and the quotes log.</li><li>Assist the Director of Sales and Marketing with quote follow-up, tracking, and filing.</li><li>Collaborate with purchasing to secure material quotes at various levels above and below current purchase quantities.</li><li>Contact new and existing outside vendors for new part quotes, including metals, resin, concentrate, ink, labels, and inserts.</li><li>Train associates in quoting processes and the information required for successful quoting.</li><li>Implement LEAN strategies to evaluate and streamline quoting operations.</li><li>Support Project Managers in tasks related to new product validations and launches.</li><li>Manage and lead projects with direct customer contact.</li><li>Assist in the development and implementation of continuous improvements in molding, tooling, printing, and other manufacturing operations.</li><li>Develop and manage project plans and activities to drive improvements.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in quoting, ERP systems, and sales order entry.</li><li>Experience in engineering administration and project management.</li><li>Strong skills in customer service and data entry.</li><li>Understanding of a manufacturing environment.</li><li>Proficiency in math, pricing, and SolidWorks.</li><li>Associates Degree in Engineering or Business Degree.</li><li>2+ years experience in costing, quoting, and manufacturing.</li><li>2+ years experience with Excel tables, formula writing, and mathematics.</li><li>Knowledge of ERP systems, especially IQMS, and IT applications.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>SOLIDWORKS proficiency desired.</li><li>Knowledge of plastic injection molding processes is a plus.</li><li>Proficiency in Microsoft Office (Excel, Word, PowerPoint, Outlook, Project).</li><li>Spanish speaking, reading, and writing bilingual ability is a plus.</li></ul><h2>Work Environment</h2><p>This role is set in a large company environment, offering opportunities for growth and experience. The workplace supports a manufacturing setting with a focus on engineering and business processes. The position requires proficiency in various IT applications and an understanding of LEAN manufacturing principles.</p>

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