<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Inspector - 2nd Shift</h1> Job DescriptionAs a Quality Inspector, you will oversee incoming component inspections, in-line and in-process checks, and issue labels for special projects. You will conduct AQL inspections in response to customer complaints and manage rework processes. Your role involves handling over 1200 samples for production lots, ensuring quality checks of medical products throughout manufacturing and packaging. You will be responsible for checking for defects in bottles, totes, caps, and other packaging, pulling labels for batch records, documenting all inspections and batch record information, and ensuring compliance with GMPs, SOPs, FDA regulations, and quality processes. Responsibilities<ul><li>Perform quality checks of medical products throughout the manufacturing and packaging process.</li><li>Inspect products for defects on bottles, totes, caps, and other packaging.</li><li>Pull labels on batch records for production personnel to use on external packaging.</li><li>Document all quality checks, inspections, and batch record information.</li><li>Ensure production personnel follow GMPs, SOPs, FDA regulations, and quality processes.</li></ul>Essential Skills<ul><li>Quality control experience.</li><li>High School Diploma.</li><li>Computer literacy in document writing (NCRs, NCMRs, Batch Record).</li><li>Legible writing and ability to work cross-functionally with production.</li><li>Verbal communication skills.</li><li>Experience with quality inspection, quality auditing, FDA inspections, GMP, FDA.</li></ul>Additional Skills &amp; Qualifications<ul><li>Understanding federal regulations is a plus.</li><li>GMP experience (can be trained).</li></ul>Work EnvironmentHours are M-F 6am-2:30pm. The company manufactures OTC drugs, cosmetics, and medical devices, primarily producing lubricating jellies, shampoos, and saline syringes. The role is split equally between floor inspections/auditing and office-based documentation and project work. The company offers paid holidays and two weeks of prorated vacation annually. It is a growing company, expanding production lines, and encourages career growth from within.

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Quality Inspector

<h1> Hiring a Construction/Quality Inspector! </h1>Job DescriptionAs an Inspector, you will perform daily site inspections of excavation, shaft activities, and linear construction within wetlands. You will ensure compliance with project specifications, safety standards, and engineering plans. Your role will involve verifying that excavation practices align with design requirements for tunneling, large shafts, and viaduct construction. Additionally, you will coordinate independent testing and enforce safety standards on-site, adhering to OSHA and other regulatory safety protocols. Responsibilities<ul><li>Conduct daily inspections of excavation, tunneling, and viaduct construction activities.</li><li>Ensure all practices align with design requirements and project specifications.</li><li>Enforce OSHA and other regulatory safety protocols, identifying potential hazards.</li><li>Inspect materials and equipment for compliance with quality standards.</li><li>Maintain detailed records of site activities, conditions, and inspection results.</li><li>Provide regular reports on progress and corrective actions taken.</li></ul>Essential Skills<ul><li>10+ years of experience in heavy civil construction, including excavation, shafts, and viaducts.</li><li>Proven ability to inspect work against specifications and drawings.</li><li>Familiarity with construction near active railroads and wetlands.</li><li>Experience in large-scale infrastructure projects.</li><li>Knowledge of OSHA and regulatory safety protocols.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bridge infrastructure experience.</li><li>Experience with city/state agencies.</li><li>Familiarity with construction near active railroads and wetlands.</li></ul>Work Environment You will collaborate closely with construction supervisors, engineers, and contractors to ensure smooth coordination of field operations. The role provides continuous on-site oversight and requires adherence to safety standards in complex environments. Benefits include 20 days of PTO, 9 holidays, and a comprehensive retirement savings plan with matching contributions. Additional perks include exclusive discounts and offers for various entertainment and travel options. Job Type &amp; LocationThis is a Permanent position based out of New York, New York.

<h1>Job Title: Mechanical Quality Inspector</h1>Job DescriptionThe Mechanical Quality Inspector is tasked with inspecting parts, assemblies, tooling fixtures, and material to ensure compliance with customer requirements, company specifications, and quality standards. You will set up, operate, inspect, test, and adjust new and reworked tools, dies, gauges, jigs, and fixtures for conformance to engineering drawings and specifications. The role also involves maintaining, processing, and updating confidential and sensitive electronic and hard copy reports, records, and statistics. This role will be working Monday-Thursday on ten hour shifts. There is optional overtime on Fridays. Responsibilities<ul><li>Inspect machined parts, components, assemblies, and materials to ensure compliance with regulatory guidelines such as Military Standards, ASTM, and ANSI.</li><li>Provide various electronic and hard copy reports of inspections and notify appropriate parties, including project engineers.</li><li>Set up and calibrate measuring and test equipment, and schedule service and repair of equipment.</li><li>Maintain calibration computer databases.</li><li>Observe testing and provide oversight to verify compliance with requirements.</li><li>Perform nondestructive examinations on various metallic and nonmetallic materials, parts, and assemblies using methods such as penetrant, hi-pot, and hardness testing.</li><li>Interact with regulatory agencies and customers during audits and reviews of company inspection and calibration activities.</li><li>Monitor and verify quality in accordance with statistical process or other control procedures.</li></ul> Qualifications<ul><li>Proficiency in inspection, quality control, quality assurance, and quality inspection.</li><li>Experience with micrometers, calipers, and other visual inspection tools.</li><li>Ability to read and understand engineering drawings and specifications.</li><li>Strong communication skills for effective interfacing with all levels of employees including management.</li><li>Ability to interpret non-routine information and respond to non-routine issues.</li><li>Capability to maintain confidentiality of sensitive information.</li><li>Good computer skills.</li><li>Hand check inspection experience.</li><li>Observation and recording as witness experience.</li><li>Experience in metal/composite inspection.</li><li>Proficiency in paperwork related to quality inspection.</li><li>Familiarity with inspection data and witness inspection.</li><li>ERP/MRP/SAP experience.</li><li>Knowledge of ISO 9001 standards.</li><li>Understanding of DOE quality assurance requirements (preferred).</li><li>Familiarity with the person Y14.5 (preferred).</li><li>Typically requires an associate&#39;s degree, trade school certificate, military training, or equivalent in quality inspections or certification by a professional group such as ASQ or AWS.</li><li>One or more years of progressive experience in electrical, mechanical, electromechanical, or metrology inspection and calibration.</li></ul> Work EnvironmentThis position is based onsite at the Tupelo Facility. This role will be working Monday-Thursday on 10 hour shifts. There is optional overtime on Fridays.

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Inspector</h1>Job DescriptionWe are seeking a diligent Quality Inspector to join our team. The ideal candidate will be responsible for ensuring products meet quality standards by inspecting and documenting various quality issues according to ISO and FDA requirements. This role involves using precision measuring instruments and working within a medical device manufacturing environment. Responsibilities<ul><li>Interpret specifications and blueprints to understand dimensional, physical, functional, and visual requirements.</li><li>Inspect products for quality issues and document findings in the ERP system per ISO and FDA standards.</li><li>Perform part inspection and measure dimensions of incoming, in-process, first piece, and finished workpieces.</li><li>Utilize precision measuring instruments, optical comparators, CMM or vision machines, along with templates and fixtures.</li><li>Assist with Corrective and Preventive Actions (CAPA), Non-Conformance Reports (NCR), and other non-conformance issues.</li><li>Collect data and enter it into spreadsheets and databases.</li><li>Support dispositions of nonconforming products, including internal issues or customer returns through the RMA procedure.</li></ul> Essential Skills<ul><li>Inspection experience</li><li>Knowledge of Quality standards</li><li>Experience with ISO 13485</li><li>Proficiency in CAPA and NCR processes</li><li>Ability to use micrometers and calipers</li><li>Minimum of 3 years of quality experience</li></ul> Additional Skills &amp; Qualifications<ul><li>Experience in a medical device manufacturing environment is beneficial</li></ul> Work EnvironmentThe position operates within a medical device manufacturer and office setting. Initial training will occur on the 1st shift (6:00am – 2:30pm, Mon-Fri) before transitioning to the 2nd shift (2:30pm – 1:00am). Potential for overtime exists depending on workflow, with an expected increase in business potentially requiring additional hours per week. Job Type &amp; LocationThis is a Contract to Hire position based out of Kenosha, Wisconsin.

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Inspector</h1>Job DescriptionWe are seeking a meticulous and experienced Quality Inspector to join our team. The role involves inspecting and verifying production hardware during Assembly, Integration &amp; Testing (AI&amp;T) to ensure compliance with drawings and specifications. The ideal candidate will apply Geometric Dimensioning and Tolerancing (GD&amp;T) principles to inspect parts and assemblies and perform incoming hardware inspections with detailed reporting. Responsibilities<ul><li>Inspect and verify production hardware during Assembly, Integration &amp; Testing (AI&amp;T).</li><li>Ensure hardware meets drawings and specifications using digital Coordinate Measuring Machines (CMM) and other inspection tools.</li><li>Apply GD&amp;T principles to inspect parts and assemblies.</li><li>Perform incoming hardware inspections and generate comprehensive reports.</li><li>Issue non-conformances for hardware that fails inspection.</li><li>Support assembly and maintenance of test equipment.</li><li>Inspect ESD components for compliance with IPC and JST standards.</li></ul> Essential Skills<ul><li>5–15 years of experience in quality inspection.</li><li>IPC-620 and J-STD-001 certifications.</li><li>Experience with ESD assemblies and CMM/Vision Machines.</li><li>Strong understanding of GD&amp;T and AS9100D standards.</li><li>Proficiency in Microsoft Office.</li><li>Ability to lift 50 lbs and climb ladders.</li><li>U.S. work authorization.</li></ul> Additional Skills &amp; Qualifications<ul><li>Experience in mechanical assembly and in-process inspections.</li><li>Receiving Inspection experience.</li><li>Experience creating, working, and resolving non-conformances.</li><li>Knowledge of CAD software, soldering, and hand tool usage.</li><li>IPC certification is a bonus.</li></ul> Work EnvironmentThe position is based in a cleanroom environment. Candidates must be able to lift up to 50 lbs and climb a 13-foot ladder. Our company offers competitive benefits, including 401k matching, full health benefits, and education reimbursement. Enjoy a work-life balance with two weeks of paid time off, which can increase with experience, and a company shutdown from Christmas to New Year’s. Job Type &amp; LocationThis is a Contract position based out of Littleton, Colorado.

Currently hiring for an Entry-Level Laboratory Technician here in the Cincinnati area! This is a long-term career opportunity and will involve quality control laboratory testing on cosmetic products. <h3>Job Duties and Responsibilities:</h3><ul><li>Perform routine testing on production batches and finished goods, following FDA/GMP standards and internal SOPs.</li><li>Use lab techniques such as HPLC, GC, TLC, wet chemistry to analyze product quality.</li><li>Record and interpret test results, spot trends, and help guide product adjustments.</li><li>Support inspections of raw materials and environmental monitoring.</li><li>Keep lab equipment calibrated and the workspace clean and organized.</li><li>Collaborate across shifts to ensure smooth communication and consistency.</li></ul><h3>Qualifications:</h3><ul><li>Bachelor’s degree in Chemistry or a related science field with strong chemistry coursework. (Required)</li><li>Industry experience in a lab setting would be a huge plus.</li></ul>

Quality Lab Technician

Actalent is hiring for an exciting opportunity in natural sciences – Seed Lab Technician Are you passionate about hands-on science and ready to make an impact in agricultural research? Join a dynamic team where your attention to detail and curiosity will help shape the future of seed science. Great opportunity for people looking for an entry level lab position! Key Responsibilities:<ul><li>Conduct visual inspections of seed samples for quality and consistency</li><li>Perform essential lab tests including pH, protein assays, moisture analysis, and titrations</li><li>Execute warm and cool germination tests</li><li>Carry out purity analysis and precise seed counts</li><li>Organize and implement standardized sampling procedures</li></ul>Schedule Details:<ul><li>Need open availability!</li><li>Spring Season (Feb–May): May include weekend work</li><li>Flexibility for 1st or 2nd shift is required</li></ul>Compensation:<ul><li>$16.00 per hour</li><li>Benefits: Health, dental, vision</li><li>401K</li></ul>Qualifications:<ul><li>High School Diploma (Required)</li><li>Valid Passport or Birth Certificate required for onboarding</li><li>Must be available to start on October 13th!</li></ul>Ready to start your lab career? Apply today! Multiple spots available!

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Lab Technician</h1>Job DescriptionWe are seeking a detail-oriented Quality Lab Technician to perform quality and chemistry-based tests, such as viscosity and specific gravity, to determine product specifications. The role involves ensuring timely quality and lab tests, documenting all necessary data, and performing algebraic calculations for product ratios and conversions. You will collaborate with production teams to inspect batch samples, packaged products, and verify product specifications, while communicating effectively with senior quality personnel to resolve issues and non-conformances. Responsibilities<ul><li>Perform quality and chemistry-based tests to determine product specifications.</li><li>Ensure quality and lab tests are conducted at the appropriate times and document all necessary data.</li><li>Perform algebraic equations to calculate ratios and conversions for various products.</li><li>Work with production to inspect batch samples and verify product specifications.</li><li>Fill out paper documentation and enter information into the quality system database.</li><li>Communicate effectively with senior quality personnel to troubleshoot issues and non-conformances.</li><li>Complete certificates of analysis, certificates of compliance, and other quality documentation as needed.</li></ul> Essential Skills<ul><li>Associate or Bachelor&#39;s degree in traditional sciences such as Chemistry or Biology.</li><li>Detail-oriented with strong time management and prioritization skills.</li><li>Ability to communicate effectively with production personnel and quality leadership.</li><li>Fortitude to make decisions regarding production pauses to ensure product quality.</li></ul> Additional Skills &amp; Qualifications<ul><li>Experience in quality control and quality assurance.</li><li>Problem-solving skills and adaptability to unique challenges.</li><li>Capability to handle multitasking and prioritize quality activities.</li></ul> Work EnvironmentThis is a 1st shift role, Monday through Friday, with no weekends, averaging 40 to 45 hours per week. General hours are from 7:00 am to 3:30 pm. The work environment offers opportunities for problem-solving with a variety of product tests and challenges. The team is tight-knit, providing a collaborative atmosphere to gain experience from the current quality team. There is a career path from Technician 1 to Technician 3, with potential for departmental growth. Training will be thorough, with guidance provided by test sheets detailing product test methods and documentation. Communication with production personnel and quality leadership is essential. A comprehensive benefits package is available once hired. Job Type &amp; LocationThis is a Contract to Hire position based out of Germantown, Wisconsin.

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Lab Technician</h1>Job DescriptionThe Quality Lab Technician will perform various quality lab test methods to ensure product quality. This role involves conducting tests such as manual titrations, pH measurements, conductivity, percent moisture loss, and utilizing equipment like particle size analyzers and FTIR. The technician will document and record all laboratory data and generate Certificates of Analysis (COA) after laboratory tests are completed and verified. Additionally, the technician will assist the Quality Manager with quality-related projects, such as SOP updates, validations, and QMS updates. Daily communication of quality test results to production and quality managers is essential. The technician will also assist with audits and maintain AS 9100 certification. Responsibilities<ul><li>Perform various quality lab test methods to ensure product quality.</li><li>Conduct tests such as manual titrations, pH, conductivity, percent moisture loss, and use particle size analyzers and FTIR.</li><li>Document and record all laboratory data.</li><li>Generate Certificates of Analysis (COA) after laboratory tests are completed and verified.</li><li>Assist the Quality Manager with quality-related projects, including SOP updates, validations, and QMS updates.</li><li>Communicate quality test results to production and quality managers daily.</li><li>Assist with audits and maintain AS 9100 certification.</li></ul> Essential Skills<ul><li>Chemistry education or lab experience.</li><li>Ability to perform titrations and pH measurements.</li><li>Proficiency in quality control and laboratory procedures.</li></ul> Additional Skills &amp; Qualifications<ul><li>Experience in dealing with quality systems and processes.</li><li>Strong communication skills to navigate and address growing pains as quality systems are improved.</li></ul> Work EnvironmentThis position is primarily based in a quality laboratory, with 90% of the time spent performing testing. There is some office work, and occasionally, the technician will go on the floor to collect samples or assist production with batch corrections. The work schedule is 1st shift, Monday through Thursday from 7 a.m. to 4 p.m., and Friday from 7 a.m. to 11 a.m. or 12 p.m. This role offers the opportunity to learn about and improve quality systems, working closely with the Quality Manager on various projects. Job Type &amp; LocationThis is a Contract to Hire position based out of Oak Creek, Wisconsin.

<h1 style="font-size: 2em; font-weight: normal;">HIRING NOW: Quality Laboratory Technician</h1>**INTERVIEWS AVAILABLE THIS WEEK**·﻿Interested in this role? Reach out directly to mbaber @actalentservices.com or CALL: 317 567 6597 withan updated resume ·*Located In Lafayette* Job DescriptionThe 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. Responsibilities<ul><li>Prepare and analyze various final product and in-process samples using analytical instruments, biology, 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>Qualifications &amp; Skills<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>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><li>Knowledge and experience with SAP is a plus.</li></ul>INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION:**INTERVIEWS AVAILABLE THIS WEEK** <ul><li>I am actively hiring and interviewing for this position TODAY - Apply today to be in consideration. I will be conducting phone interviews as early as today. All candidates will be considered within 24 hours of reaching out directly to Morgan Baber</li><li>Apply to Morgan Baber at mbaber @actalentservices. com or CALL(317-567 -6597) with your updated resume, brief intro about your interest, what method of communication works best for you(i.e., call, email, text)</li></ul>

Quality Laboratory Technician

<h1>HIRING NOW: Quality Laboratory Technician</h1>**INTERVIEWS AVAILABLE THIS WEEK**﻿Interested in this role? Reach out directly to mrichey@actalentservices .com or CALL: 317 567 6591 with an updated resume ·*Located In Lafayette* Job DescriptionThe 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. Responsibilities<ul><li>Prepare and analyze various final product and in-process samples using analytical instruments, biology, 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>Qualifications &amp; Skills<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>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><li>Knowledge and experience with SAP is a plus.</li></ul>INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION:<ul><li>I am actively hiring and interviewing for this position TODAY - Apply today to be in consideration. I will be conducting phone interviews as early as today. All candidates will be considered within 24 hours of reaching out directly to Max Richey</li><li>Apply to Max Richey at mrichey@actalentservices. com or CALL(317-567 -6591) with your updated resume, brief intro about your interest, what method of communication works best for you(i.e., call, email, text)</li></ul>

<h2 style="text-align: center;">Immediate Opening: Quality Laboratory Technician – Entry Level</h2>Location: Lafayette, INWork Type: On-site |Rotating 12-hour shifts | Contract-to-Hire<h2>Position Summary</h2>Join a leading manufacturer of sweeteners and starches as a Quality Laboratory Technician, where you&#39;ll gain hands-on experience in analytical chemistry and microbiology. This entry-level role is ideal for recent graduates or early-career professionals eager to grow in a fast paced lab environment supporting human and animal feed production. Key Responsibilities<ul><li>Analyze final product and in-process samples using advanced instrumentation: HPLC, GC, AA, FT-IR, NIR, Karl Fischer, and more</li><li>Perform wet chemistry techniques, extractions, and “wetmills” on liquid products</li><li>Conduct microbiological testing, pH analysis, refractive index, particle size distribution, and spectrophotometric methods</li><li>Post results into data systems and communicate findings to plant personnel</li><li>Identify abnormal results and collaborate with process teams to resolve issues</li><li>Perform QA/QC checks on outbound shipments and document results</li><li>Maintain lab equipment and follow established methodologies</li><li>Support cross-functional teams with analytical and project-based tasks</li><li>Adhere to company policies, safety protocols, and core values</li><li>Participate in skill block training to advance lab technician levels and compensation</li></ul>Required Qualifications<ul><li>Bachelor’s degree in Chemistry, Biology, or related scientific discipline</li><li>Familiarity with lab instrumentation and methodologies (experience may come from coursework or internships)</li><li>Willingness to work a 24/7 rotating shift schedule (including nights, weekends, and holidays)</li><li>Strong attention to detail, troubleshooting ability, and self-motivation</li><li>Excellent communication skills and ability to multitask</li><li>Proficiency in Microsoft Office; SAP experience is a plus</li></ul>Preferred Skills<ul><li>Experience with titrations, wet chemistry, viscosity testing, microbiology</li><li>Understanding of GMP standards and quality control procedures</li></ul> Work Environment<ul><li>12-hour rotating shifts: 3 days on, 3 days off (e.g., 5am–5pm, then 5pm–5am)</li><li>Comfortable standing for extended periods</li><li>Casual dress code: jeans and t-shirt acceptable</li><li>Collaborative team culture with training and growth opportunities</li></ul>Career Growth &amp; Compensation<ul><li>Begin training immediately on skill blocks to advance technician levels</li><li>Level I technicians earn up to $27/hour</li><li>Top-tier lab techs can earn up to $100K+ annually based on skill competencies</li></ul> Ready to Apply?We’re actively interviewing for this position!To apply directly: Email your resume and a briefintroduction (including your preferred contact method: call, email, or text) toAbby Vaughn at abvaughn @actalentservices.com Or call (317 -567 -6605) to speak with Abby.

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Manager</h1>Job DescriptionWe are seeking a dedicated Quality Manager to maintain and enhance our ISO 9001-certified Quality Management System. This role is pivotal in ensuring compliance with ISO standards and aligning them with our business operations. You will lead internal audit planning, coordinate third-party audits, and manage corrective actions while fostering a culture of continuous improvement. Responsibilities<ul><li>Maintain and improve the ISO 9001-certified Quality Management System, ensuring compliance and alignment with business operations.</li><li>Lead internal audit planning and execution, coordinate third-party surveillance audits, and ensure follow-up corrective actions to maintain ISO certification status.</li><li>Update and control documented procedures and forms across departments.</li><li>Coordinate annual management review meetings and quality objectives reporting.</li><li>Maintain a centralized tracking system for the internal calibration of tools and measurement equipment, ensuring timely calibration and documentation.</li><li>Manage the Corrective Action Report (CAR) process for customer-reported and internally identified nonconformities.</li><li>Collaborate with internal teams to identify root causes using problem-solving tools such as 5 Whys and fishbone diagrams.</li><li>Prepare formal CAR responses to customers, including containment, root cause analysis, corrective actions, and effectiveness verification.</li><li>Issue and track Supplier Corrective Action Requests (SCARs) for vendor-related defects, ensuring timely and effective closure.</li><li>Collaborate with the Sales team to provide accurate, timely updates to customers throughout the corrective action process.</li><li>Respond to customer requests for material compliance documentation, including RoHS, REACH, and Conflict Minerals reports.</li><li>Maintain records and templates for fast, accurate turnaround of compliance responses.</li></ul> Essential Skills<ul><li>Strong understanding of ISO 9001 Quality Management System principles.</li><li>Familiarity with regulatory compliance topics, including RoHS, REACH, and Conflict Minerals.</li><li>Experience managing corrective actions (CAR/SCAR) with problem-solving and testing to confirm root causes.</li><li>Excellent written communication skills for customer-facing CAR responses.</li><li>Proficiency in Microsoft Office, including Excel, Word, and Outlook.</li></ul> Additional Skills &amp; Qualifications<ul><li>Experience with SharePoint and Power BI is a plus.</li><li>Detail-oriented, organized, and responsive under deadlines.</li><li>Ability to work independently and cross-functionally across departments.</li></ul> Work EnvironmentJoin a company with an employee-owned culture that offers an employee ownership model in stock. The company invests in its employees by paying for certain certifications and providing education reimbursement. Job Type &amp; LocationThis is a Contract position based out of Saint Louis, Missouri.

Quality Manager

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Manager</h1> Job DescriptionResponsible for overseeing the Quality Department and direct reports, ensuring the overall quality of our products. Responsibilities<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>Essential Skills<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>Additional Skills &amp; Qualifications<ul><li>Experience with quality inspection, harness, and cable harness.</li></ul>Work EnvironmentThis 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.

Actalent Engineering is hiring a Quality Control Manager for a great company in Oregon City. This is a long-term job opportunity! Job DescriptionThe QA/QC Manager will support a family-owned fabrication shop that produces various steel products for a range of industries. They will have experience on the shop floor and will also oversee all activities and requirements of a Quality Management System. Key Responsibilities and Required Skills:<ul><li>Manage QA/QC documentation and processes</li><li>Complete hands-on quality control inspections and documentation</li><li>Create and update weld procedures</li><li>Weld inspection experience (CWI not required)</li><li>Experience working within and managing a Quality Management System</li><li>Manage flow and associated documentation for parts within different stages and processes (some outsourced)</li><li>Utilize strong GD&amp;T experience</li><li>Manage a team of 4-6 inspectors</li></ul> Skills &amp; QualificationsRequired Skills:<ul><li>Weld inspection experience (CWI not required)</li><li>Experience writing welding procedures (highly preferred)</li><li>Experienced in blueprint reading and layout, along with inspecting welds</li><li>Hands-on experience various using various measuring tools including calipers, weld gauges, micrometers and completing associated documentation</li><li>Understanding and experience of managing parts within different stages and processes</li><li>Strong GD&amp;T experience</li></ul>Nice to Have:<ul><li>Experience managing a team of inspectors</li></ul>

<h1>Job Title: Quality Assurance Manager - Putnam, CT </h1>Job DescriptionWe are seeking a detail-oriented and experienced Quality Assurance Manager to join our team. The ideal candidate will play a crucial role in ensuring that our products meet the highest quality standards. This position involves conducting quality audits, utilizing precision measuring instruments, and maintaining industry compliance standards. The Quality Assurance Manager will work closely with production teams to identify areas for development, improvement and ensure adherence to quality management systems. Responsibilities<ul><li>Conduct regular quality audits to assess compliance with established standards and procedures.</li><li>Utilize precision measuring instruments and coordinate measuring machines to perform inspections on products.</li><li>Collect and analyze data related to product quality, identifying trends and areas for improvement.</li><li>Ensure all processes align with standards and maintain documentation of quality control activities.</li><li>Collaborate with production teams to implement corrective actions based on inspection findings.</li><li>Assist in the development and maintenance of quality systems to enhance overall product reliability.</li></ul> Essential Skills<ul><li>QA experience in a manufacturing environment.</li><li>Thorough understanding of part measuring techniques and equipment.</li><li>Quality data analysis experience supporting quality metrics, trends, and reporting.</li><li>Supervisory experience.</li><li>Can-do attitude, not afraid of hands-on tasks on the shop floor.</li></ul> Additional Skills &amp; Qualifications<ul><li>Proven experience in quality assurance or quality control roles within a manufacturing environment.</li><li>Strong knowledge of quality audits and quality management principles.</li><li>Proficiency in using precision measuring instruments and coordinate measuring machines.</li><li>Familiarity with data collection techniques and analysis methods related to product quality.</li><li>Experience with software for inspection and reporting is preferred.</li><li>Excellent attention to detail, analytical skills, and problem-solving abilities.</li><li>Strong communication skills, both verbal and written, to effectively collaborate with team members across departments.</li></ul> Work EnvironmentThis position will have one direct report (QA tech) with anticipation for department growth. The work environment encourages a collaborative approach, with opportunities to build a department within a growing company.

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Manager</h1>Job DescriptionEnsure that the organization’s Quality Management System conforms to several customers, internal, and 3rd party audits, including ISO9001 and IATF16949. Manage the monitoring, measurement, and review of internal processes through internal audits. Drive continuous improvement initiatives to ensure that process owners meet key performance indicator goals. Conduct annual Management Review Meetings and maintain the Document Control Program. Responsibilities<ul><li>Manage and monitor the Training Program.</li><li>Oversee the Internal Audit Program.</li><li>Supervise QA Inspectors and QA Specialists.</li><li>Execute customer complaint investigations and respond to customers.</li><li>Monitor APQPs and PPAPs.</li><li>Conduct all required internal and external meetings.</li><li>Facilitate yearly training on the Quality Management System.</li></ul> Essential Skills<ul><li>Quality engineering experience.</li><li>Proficiency with PPAP, ISO9001, and IATF.</li><li>Experience with corrective actions.</li><li>Familiarity with fast-paced/high-volume manufacturing environments.</li><li>Proficient in QMS and 8D problem-solving methodologies.</li></ul> Additional Skills &amp; Qualifications<ul><li>10+ years in a manufacturing environment.</li><li>5 years of direct experience in overseeing process design, development, and implementation of a Quality System such as ISO 9001 or IATF16949.</li><li>Strong interpersonal, written, and verbal communication skills.</li><li>Excellent organizational skills and initiative.</li><li>Ability to work well without supervision.</li><li>Experience with ERP systems.</li><li>Proficiency in Microsoft Word and Excel.</li><li>Lean Manufacturing knowledge, including 5S, Green/Black Belt, 6 Sigma, and experience with 8D Reports.</li></ul> Work EnvironmentThe position operates in a fast-paced, high-volume manufacturing environment. The role requires proficiency with modern technologies and methodologies such as Lean Manufacturing, 5S, and 6 Sigma. The use of ERP systems, Microsoft Word, and Excel is integral to daily operations. Job Type &amp; LocationThis is a Permanent position based out of Santa Fe Springs, California.

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Manager</h1>Job DescriptionJoin our team as a Quality Manager for a brand new power plant project, focusing on the construction of a Simple Cycle 3F class Siemens CT plant. This full-time, field-based position requires overseeing electrical inspection and quality control to ensure compliance with applicable codes, standards, and specifications. You will work closely with contractors to resolve discrepancies and ensure successful project execution. Responsibilities<ul><li>Control and distribute all company quality documentation.</li><li>Monitor all quality-related activities on the project.</li><li>Perform daily inspections of onsite work.</li><li>Conduct internal and external audits on behalf of management.</li><li>Verify contractor quality requirements and review documentation submittals.</li><li>Review qualifications and training requirements of quality inspection personnel.</li><li>Monitor the disposition of issued nonconformance reports.</li><li>Assess the progress and effectiveness of the project quality management system, recommending improvements when necessary.</li><li>Review and comment on quality-related correspondence with contractor representatives.</li><li>Monitor statistical method reporting.</li><li>Review all turnover documentation upon project completion.</li><li>Participate in quality-related activities with designated representatives.</li><li>Attend meetings and provide insights on quality-related subjects.</li></ul> Essential Skills<ul><li>5 years of experience in construction quality management.</li><li>Strong attention to detail.</li><li>Strong conflict resolution skills.</li><li>Prior utility experience.</li><li>Willingness to travel.</li><li>Ability to plan and execute highly complex operations independently.</li><li>Strong problem-solving and analytical skills.</li><li>Strong prioritization and organizational skills.</li><li>Excellent verbal and written communication skills.</li><li>Proficiency in Microsoft Office programs.</li><li>Ability to work effectively in a diverse and inclusive environment.</li></ul> Additional Skills &amp; Qualifications<ul><li>Experience with simple cycle or similar power plant construction (Siemens, 3F turbines, RICE plants, etc.).</li><li>Construction management background preferred but not required.</li></ul> Work EnvironmentThe Quality Manager will be required to work on site 5-6 days a week for a duration of 5-7 years at two locations: Cedar Rapids and Burlington. These sites are new generation plants with Cedar River Generating Station being a natural gas electric generating facility with a capacity of approximately 94 net megawatts. The project involves five Wärtsilä W18V50SG RICE generators, each with a nominal capacity of 18.8 MW. This role offers the opportunity to work directly for the utility, with GSA per diem rates and optional mileage reimbursement. Job Type &amp; LocationThis is a Contract position based out of Madison, Wisconsin.

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Manager</h1> Job DescriptionThe Quality Manager will play a crucial role in designing, implementing, monitoring, and improving the Quality Management System (QMS) in accordance with industry standards. This role is pivotal in ensuring the company achieves its quality targets and maintains compliance with regulatory requirements. Responsibilities<ul><li>Support the design, implementation, monitoring, and improvement of the Quality Management System (QMS) according to ISO9001:2015 standards.</li><li>Manage Supplier Development, Incoming Inspection, Non-Conformities, Product Quality Control, and Machines Final Control (Product Audit) processes.</li><li>Actively participate in supplier qualification and regularly monitor supplier performance.</li><li>Collect and process data from Incoming Inspection, production control, and installation and service reports to analyze product and process quality.</li><li>Manage Corrective and Preventive Actions.</li><li>Enforce regulatory compliance with relevant quality standards and regulations, prepare for audits, and maintain accurate quality records.</li><li>Perform in-process quality checks to ensure products are ready for customer use and meet quality standards.</li></ul>Essential Skills<ul><li>Quality management</li><li>Supplier quality</li><li>Root cause analysis</li><li>Corrective action plans</li><li>Quality management system</li><li>Quality engineering</li></ul>Additional Skills &amp; Qualifications<ul><li>BS in Engineering required</li><li>3-5 years of Quality Engineering/Management experience</li><li>3-5 years of Quality Experience in a Machining environment</li><li>Experience with Corrective and Preventive Actions</li><li>Familiarity with ISO9001 and AS9100 standards</li></ul>Work EnvironmentThe role is within a small to midsize company of about 50 employees, where every product manufactured is custom for various industries. The environment includes collaboration with customers to develop ideas, create and design CAD models, and conduct testing. The company boasts a strong culture with opportunities for upward mobility and international travel. The work environment involves a machine shop setting with CNC machines. Job Type &amp; LocationThis is a Permanent position based out of Minnesota.

<h1>Hiring a Quality Manager in the Aerospace Industry</h1> Job DescriptionWe are seeking a dynamic Quality Manager to oversee the supervision of quality inspectors, coordinate workload schedules, and drive employee development and training. The role involves managing the inspection function to ensure compliance with all quality standards and the conformance of all products to applicable specifications before release to inventory. The Quality Manager will also focus on minimizing cycle time and optimizing efficiency while maintaining compliance with all quality policies and standards. Responsibilities<ul><li>Supervise quality inspectors and coordinate workload schedules.</li><li>Manage the inspection function to ensure compliance with quality standards and product specifications.</li><li>Optimize inspection processes to minimize cycle time and maintain efficiency.</li><li>Maintain compliance with FAA regulations, ISO, AS standards, and internal quality requirements.</li><li>Facilitate effective communication between upstream and downstream stakeholders to resolve issues promptly.</li></ul>Essential Skills<ul><li>5+ years of professional experience in Quality engineering.</li><li>Experience in regulated industries.</li><li>Proficiency in Quality Management Systems (QMS).</li><li>Ability to conduct root cause analysis.</li><li>Bachelor&#39;s degree in engineering.</li></ul>

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Manager</h1>Job DescriptionThe Quality Manager is responsible for leading all site-level quality and food safety operations at the Massachusetts manufacturing site, which specializes in producing annatto-derived ingredients through distillation. This role serves as the site authority on quality systems and regulatory compliance, overseeing the implementation of the Food Safety Plan and ensuring compliance with all applicable FDA regulations (21 CFR 111 and 117). Additionally, the Quality Manager manages the site Quality Management System (QMS) and quality responsibilities for warehouse and production activities. The role also involves overseeing quality-related activities with co-manufacturers and ensuring supply chain preventive control, including approval and Foreign Supplier Verification Program (FSVP) compliance. Responsibilities<ul><li>Promote a strong culture of quality and food safety throughout the site.</li><li>Serve as the site Preventive Controls Qualified Individual and manage the Food Safety Plan in accordance with regulatory standards.</li><li>Manage the site Preventive Controls-based Food Safety and Quality Management System (FSQMS), including SOPs, change control, training, and document control.</li><li>Oversee training programs for GMPs, HACCP/Food Safety, and Food Defense/Food Fraud.</li><li>Manage validation and verification activities of the site, including sanitation validation and verification, internal inspections, and environmental monitoring.</li><li>Manage the recall program and ensure traceability is maintained throughout the supply chain.</li><li>Manage contractors associated with food safety, such as Pest Control, Sanitation, and uniforms.</li><li>Review and approve production batch records, ensuring compliance with specifications and regulatory requirements.</li><li>Handle production nonconformities according to site SOPs, and address deviations, corrective, and preventive actions when applicable.</li><li>Lead investigations into incidents, quality issues, and complaints.</li><li>Oversee QA processes related to on-site warehouse activities, including receiving, sampling, repacking, and storage.</li></ul> Essential Skills<ul><li>Quality assurance</li><li>Quality control</li><li>Quality management</li><li>Food safety</li><li>Knowledge of 21 CFR 111 and 21 CFR 117</li></ul> Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in food science, Chemistry, Biology or related technical field (advanced degree preferred)</li><li>Minimum 10 years of progressive quality assurance experience in food, dietary supplements, or ingredient manufacturing</li><li>PCQI certified with experience in overseeing product release, production records review, and QA in a manufacturing environment</li><li>Knowledge of supplier quality management and FSVP requirements</li><li>Excellent communication, documentation, and leadership skills</li><li>Proficiency in Microsoft Office (Word, Excel, PowerPoint, Access); project management tools a plus</li><li>Excellent analytical, communication, and problem-solving skills</li></ul> Work EnvironmentThe position is based on-site, with working hours from Monday to Friday, 8:30 am to 4:30 pm. Job Type &amp; LocationThis is a Permanent position based out of Hadley, Massachusetts.

Quality Manager- Food

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Specialist</h1>Job DescriptionWe are seeking a dedicated Quality Specialist to join our dynamic team within a rapidly growing Cell and Gene Therapy CDMO at a brand new site. In this role, you will ensure compliance with quality objectives and regulatory requirements while supporting manufacturing and technical operations. Responsibilities<ul><li>Provide on-floor Quality Operations support for manufacturing, warehouse, and other technical operations, including in-process checks, deviation identification, and adherence to cGMP expectations.</li><li>Ensure all manufacturing activities comply with GMP and regulatory requirements.</li><li>Review and approve GMP documentation such as batch records, SOPs, test methods, validation protocols, and technical reports for accuracy and compliance.</li><li>Execute product-related activities, including apheresis material receipt, raw material disposition, production document issuance, batch review, and final product disposition and shipment.</li><li>Lead and drive investigations into deviations, non-conformances, environmental excursions, and process anomalies.</li><li>Apply structured root cause analysis tools such as 5 Whys, Fishbone (Ishikawa), and FMEA to support investigations.</li><li>Collaborate cross-functionally with Manufacturing, Quality Control, and Supply Chain teams to resolve quality issues.</li><li>Support continuous improvement initiatives to enhance quality, compliance, and operational efficiency.</li><li>Participate in and support internal audits, facility walkthroughs, and regulatory inspections.</li></ul> Essential Skills<ul><li>3+ years of cell therapy experience.</li><li>3-5 years of GMP manufacturing experience.</li><li>Experience in Quality Assurance oversight for manufacturing floors.</li><li>Proficient in ISO 7 gowning procedures.</li><li>Bachelor’s degree in a relevant scientific discipline with 5+ years of experience in the pharmaceutical or GMP industry.</li><li>5-7 years of QA experience in a GMP-regulated environment, ideally with cell therapy, gene therapy, or other advanced biologics.</li><li>Strong knowledge of batch record review, aseptic operations, and environmental monitoring.</li><li>Demonstrated ability to lead and close complex quality investigations including root cause analysis and development of effective CAPAs.</li></ul> Additional Skills &amp; Qualifications<ul><li>CDMO experience is strongly preferred.</li><li>Strong knowledge of cGMP regulations (21 CFR Parts 210, 211, 1271), and relevant ICH and FDA guidance.</li><li>Proficient in investigation tools and methodologies such as Fishbone diagrams, 5 Whys, and FMEA.</li><li>Excellent problem-solving skills with a focus on risk-based decision-making and continuous improvement.</li><li>Ability to understand technical concepts and make informed quality decisions in clinical manufacturing.</li><li>Willingness to work in ISO 7 environments for on-the-floor QA support.</li><li>Proactive, adaptable, and committed to continuous learning.</li><li>Flexibility to travel between facilities and work varying hours, including evenings, weekends, and shifts as needed.</li></ul> Work EnvironmentWork at a growing CDMO specializing in Cell and Gene Therapy at a brand new site. This position requires working in ISO 7 environments and may involve varying work hours, including evenings, weekends, and shifts. The role involves being actively present on the manufacturing floor, supporting operational excellence and contributing to a collaborative team-oriented environment. Job Type &amp; LocationThis is a Permanent position based out of NA, New Jersey.

Quality Specialist

<h1>Job Title: Quality Specialist II</h1>Job DescriptionJoin a dynamic team that serves as the first line of defense for quality assurance in a rapidly growing, state-of-the-art facility. Although this role is not lab-based, it plays a crucial part in providing guidance, reviewing batch records, and determining the course of action for discrepancies. You will operate within the Quality Management System to ensure compliance and accuracy in the manufacture of phase-appropriate materials. Responsibilities<ul><li>Operate within the Quality Management System applicable to the manufacture of phase-appropriate material.</li><li>Ensure all product samples are adequately labeled and document all aspects of sample allocation and transition.</li><li>Maintain full accountability for product allocation across sample requirements and storage conditions.</li><li>Evaluate processes associated with sample management to identify gaps and implement improvements.</li><li>Ensure documentation is completed, reviewed, filed, and archived according to Standard Operating Procedures (SOPs).</li><li>Maintain compliance with applicable regulatory requirements for cellular and gene therapy products.</li><li>Perform tasks in accordance with established policies, procedures, and techniques under the supervision of staff.</li><li>Collaborate effectively within a diverse and cross-functional team environment.</li><li>Document all activities performed according to GMP, cGMP, GLP, QC, and other relevant standards.</li></ul> Essential Skills<ul><li>Bachelor&#39;s degree in Biology or related science field.</li><li>Experience in a highly regulated environment with strong documentation practices.</li><li>Preferred experience in a GMP environment, but experience from other regulated environments such as GLP is also considered.</li></ul> Additional Skills &amp; Qualifications<ul><li>Technical writing skills.</li><li>Experience with investigations and CAPAs.</li><li>Ability to work under supervision and follow established procedures.</li></ul> Work EnvironmentWork primarily at a desk with cleanroom visits about twice a week. Collaborate within a team of 9-10 people in a rapidly growing company building new sites in Columbus, Ohio. The facility features state-of-the-art clean rooms and equipment. The role is almost entirely onsite with flexible hours between 8am-5pm, allowing for personal commitments. Weekend work is on a voluntary basis to address backlog. Job Type &amp; LocationThis is a Contract to Hire position based out of Columbus, Ohio.

Quality Specialist II

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Supervisor</h1>Job DescriptionAs a Quality Supervisor, you will oversee the quality control inspectors during your assigned shift. This role involves handling all personnel and policy-related matters. You will ensure that teams adhere to established procedures for addressing quality control issues promptly by providing on-the-floor support. You will also coordinate the control of products during inspection and disposition, including making critical decisions such as halting production or holding products when necessary. Responsibilities<ul><li>Supervise and support a team of 3-4 quality control inspectors.</li><li>Ensure compliance with quality control procedures and timely issue resolution.</li><li>Coordinate product inspection and disposition processes.</li><li>Lead initial investigations into production issues and non-conformances.</li><li>Assign tasks and manage schedules under the guidance of the QA Manager.</li><li>Train new quality control employees on testing procedures and safety practices.</li><li>Manage daily quality assurance activities in manufacturing and product inspection.</li><li>Provide feedback and recommend procedural improvements to management.</li><li>Implement testing procedures as per managerial guidance and industry standards.</li><li>Perform quality control inspection duties when necessary, including measurements and visual inspections.</li></ul> Essential Skills<ul><li>Proficiency in quality assurance and control processes.</li><li>Experience with inspection tools such as calipers and micrometers.</li><li>Strong problem-solving skills and experience in root cause analysis.</li><li>Demonstrated ability to investigate non-conformances.</li><li>3-10 years of quality experience in an FDA-regulated field, preferably in medical devices or pharmaceuticals.</li><li>High School Diploma.</li></ul> Additional Skills &amp; Qualifications<ul><li>Quality mindset and strong leadership skills.</li><li>Experience in quality leadership roles (Team Lead/Supervisor) for at least 2 years.</li><li>Familiarity with personnel management and handling personnel issues.</li></ul> Work EnvironmentThe facility is large and divided into various areas based on product types such as disposable, reusable, device, and chemical mixing. It is a clean and compliant environment. The role involves spending significant time on the production or receiving floor, with temperature-controlled conditions. You will be on your feet for most of your shift. The shift schedule is Monday to Friday, 3:00 PM to 11:30 PM, with occasional interaction with the 3rd shift as needed. Initial training will be conducted on the first shift for the first 3-4 weeks. Job Type &amp; LocationThis is a Permanent position based out of Earth City, Missouri.

Quality Supervisor

DescriptionWe currently seek a Quality Systems Engineer to join our division located in Avon, CT, and help support our continued business growth. This position is responsible for the implementation, maintenance, and improvement of quality processes and systems within the organization. The QSE ensures that products and processes consistently meet industry standards, customer, and regulatory requirements. Essential duties and responsibilities include, but are not limited to:Implement and maintain best practices for quality processes and systems: This involves working closely with various departments to ensure consistency and standardization.Business system improvement: Identifying areas for improvement based on internal audits and implementing corrective actions.Oversee Quality Systems Certification: Managing certifications like ISO and AS9100, and overseeing internal and external audits.Ensure Internal Quality Systems Compliance: Deploying and ensuring efficient use of internal quality systems such as Corrective &amp; Preventative Action (CAPA) and Change Control Management.Manage Standard Work Development &amp; Maintenance: Creating and updating standard operating practices and documentation within the Quality Management System (QMS).Customer Facing Quality Systems Interface: Coordinating compliance with customer-specific quality system requirements.Lead Auditing program: Conducting internal audits and driving the continuous sustainability of the quality system.Promote Compliance &amp; Ethical Behavior: Maintaining a high standard for quality compliance and ethical conduct, and training others on these subjects.Problem-solving and Corrective Action: Participating in brainstorming and implementing plans to address quality issues. Lead Quality Training program: Implement training best practices and provide and coordinate training to quality systems procedures.SkillsQuality assurance, Quality engineering, Iso 13485, iso 9001, Root cause analysis, Quality management system, fiber optic, fiber optic cableTop Skills DetailsQuality assurance, Quality engineering, Iso 13485,iso 9001, Root cause analysis, Quality management systemExperience LevelIntermediate Level

Quality Systems Engineer

Description
					We currently seek a Quality Systems Engineer to join our division located in Avon, CT, and help support our continued business growth.

This position is responsible for the implementation, maintenance, and improvement of quality processes and systems within the organization. The QSE ensures that products and processes consistently meet industry standards, customer, and regulatory requirements.

Essential duties and responsibilities include, but are not limited to:

Implement and maintain best practices for quality processes and systems: This involves working closely with various departments to ensure consistency and standardization.
Business system improvement: Identifying areas for improvement based on internal audits and implementing corrective actions.
Oversee Quality Systems Certification: Managing certifications like ISO and AS9100, and overseeing internal and external audits.
Ensure Internal Quality Systems Compliance: Deploying and ensuring efficient use of internal quality systems such as Corrective &amp; Preventative Action (CAPA) and Change Control Management.
Manage Standard Work Development &amp; Maintenance: Creating and updating standard operating practices and documentation within the Quality Management System (QMS).
Customer Facing Quality Systems Interface: Coordinating compliance with customer-specific quality system requirements.
Lead Auditing program: Conducting internal audits and driving the continuous sustainability of the quality system.
Promote Compliance &amp; Ethical Behavior: Maintaining a high standard for quality compliance and ethical conduct, and training others on these subjects.
Problem-solving and Corrective Action: Participating in brainstorming and implementing plans to address quality issues. 
Lead Quality Training program: Implement training best practices and provide and coordinate training to quality systems procedures.
					Skills
					Quality assurance, Quality engineering, Iso 13485, iso 9001, Root cause analysis, Quality management system, fiber optic, fiber optic cable
					Top Skills Details
					Quality assurance,Quality engineering,Iso 13485,iso 9001,Root cause analysis,Quality management system
					
					
					Experience Level
					Intermediate Level

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Specialist</h1>Job DescriptionWe are seeking a dedicated Quality Specialist to lead the design, implementation, and maintenance of food safety and quality systems. This role ensures compliance with regulatory standards and manages both internal and external audits. The successful candidate will oversee quality control processes and collaborate with cross-functional teams to support new product introductions and process improvements. Responsibilities<ul><li>Lead the design, implementation, and maintenance of food safety and quality systems such as HACCP, GMP, SQF, and GFSI.</li><li>Ensure compliance with FDA, USDA, and other applicable regulatory bodies.</li><li>Manage internal and external audits, including customer and third-party inspections.</li><li>Oversee quality control processes for raw materials, in-process, and finished goods.</li><li>Investigate consumer complaints and non-conformances; conduct root cause analysis and implement corrective actions.</li><li>Develop and monitor KPIs related to food safety and quality performance.</li><li>Train and mentor QA staff and production teams on quality standards and procedures.</li><li>Maintain documentation systems and ensure traceability and record-keeping compliance.</li><li>Collaborate cross-functionally with R&amp;D, Operations, and Supply Chain to support new product introductions and process improvements.</li></ul> Essential Skills<ul><li>Experience with quality systems and food safety.</li><li>Proficiency in quality management systems.</li><li>Knowledge of HACCP, SQF, and GFSI.</li><li>Document control experience.</li><li>Familiarity with GMP and FSMA regulations.</li><li>Ability to perform allergen testing and implement food defense strategies.</li></ul> Additional Skills &amp; Qualifications<ul><li>Completed Chemical Safety Training within the past 12 months.</li><li>Attended GMP, FSMA, Food Defense Awareness, and Allergen Training.</li><li>Compliance with SQF Program requirements.</li><li>PCQI training and intentional adulteration training.</li><li>Adherence to all GMP Requirements and Safety Rules and Policies.</li></ul> Work EnvironmentThe Quality Specialist will work in a dynamic environment that requires strict adherence to safety and regulatory guidelines. The role involves collaboration with various departments, including R&amp;D, Operations, and Supply Chain, to ensure product quality and safety. Personal Protective Equipment must be worn as defined by plant procedures. Job Type &amp; LocationThis is a Permanent position based out of Saint Louis, Missouri.

Quality Systems Specialist

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Systems Supervisor</h1> Job DescriptionSupervise QA/QC and sanitation programs across the facility. Lead internal and external audit preparation and execution. Train and mentor a team of six lab technicians. Maintain and improve documentation accuracy, compliance, and control. Conduct root cause analysis for micro passing rate issues. Manage and reduce customer complaints through proactive quality measures. Oversee vendor approval processes and incoming material evaluations. Ensure calibration and standardization of chemistry instruments. Collaborate with production and engineering teams to improve safety scores. Participate in onboarding activities including shadowing, audit support, and internal scoring. Responsibilities<ul><li>Supervise QA/QC and sanitation programs across the facility.</li><li>Lead internal and external audit preparation and execution.</li><li>Train and mentor a team of six lab technicians.</li><li>Maintain and improve documentation accuracy, compliance, and control.</li><li>Conduct root cause analysis for micro passing rate issues.</li><li>Manage and reduce customer complaints through proactive quality measures.</li><li>Oversee vendor approval processes and incoming material evaluations.</li><li>Ensure calibration and standardization of chemistry instruments.</li><li>Collaborate with production and engineering teams to improve safety scores.</li><li>Participate in onboarding activities including shadowing, audit support, and internal scoring.</li></ul>Essential Skills<ul><li>Strong understanding of food safety, sanitation, and regulatory compliance.</li><li>Experience maintaining and auditing food safety systems.</li><li>Ability to manage, create, and audit documentation for legal and regulatory accuracy.</li><li>Leadership development, communication, and leadership skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>2–5 years of supervisory experience in quality, sanitation, or lab environments.</li><li>Strong lab experience with ability to lead audit preparations.</li><li>Excellent documentation and communication skills.</li><li>Ability to multitask and remain calm under pressure.</li><li>Familiarity with chemistry standardization and calibration.</li><li>Experience in document control and legal compliance.</li><li>Experience in the dairy industry.</li><li>Familiarity with CIP review processes.</li><li>Knowledge of FT120 Dairy Analyzer.</li><li>Knowledge of Quality Systems.</li><li>Experience managing lab teams.</li></ul>Work EnvironmentThe environment is structured but fast-moving, with high expectations for multitasking, documentation accuracy, and regulatory readiness. Employees are expected to be self-motivated, able to handle pressure, and comfortable with shifting priorities. The Quality Systems team, including lab techs and supervisors, operates in a high-compliance, detail-driven setting. There’s a strong emphasis on training, mentorship, and continuous improvement, especially for new hires or those stepping into leadership roles.

Quality Systems Supervisor

<h1 style="font-size: 2em; font-weight: normal;">Job Description: Quality Technician</h1>We are seeking a dedicated Quality Technician to join our team. The ideal candidate will have an Associate&#39;s Degree, though this is preferred and not mandatory, and 0-3+ years of experience in a regulated industry such as medical, aerospace, or automotive. The role primarily involves reviewing product non-conformances and completing quality documentation related to part defects and inspection plans. Responsibilities<ul><li>Review product non-conformances and complete quality documentation.</li><li>Understand technical drawings, dimensions, and required specifications.</li><li>Utilize inspection tools including micrometers, calipers, and gauges.</li><li>Communicate with operators on the production floor regarding non-conforming materials.</li><li>Assist with supplier change request forms, FMEA, PPAPs, and other quality documentation.</li><li>Use Excel for data collection and analysis.</li><li>Split time between office work (50%) and production floor activities (50%).</li></ul>Essential Skills<ul><li>Experience in quality inspection and documentation.</li><li>Proficiency in using calipers, micrometers, and gauges.</li><li>Understanding of technical drawings and CAD.</li><li>Ability to handle non-conformances and conduct defect analysis.</li><li>Excellent communication skills and attention to detail.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with PPAP and FMEA processes.</li><li>Familiarity with electro-mechanical assembly environments.</li></ul>

Quality Techncian

<h1>Job Title: Quality Technician</h1>Job DescriptionWe are seeking a dedicated Quality Technician to join our team. The ideal candidate will have an associate degree and 0-3+ years of experience working in a regulated industry such as medical, aerospace, or automotive. This role involves reviewing product non-conformances and completing quality documentation related to part defects and inspection plans. The successful candidate will have a solid understanding of technical drawings, dimensions, and required specifications, and the ability to use inspection tools such as micrometers, calipers, and gages. Responsibilities<ul><li>Review product non-conformances and complete quality documentation for part defects and inspection plans.</li><li>Understand and interpret technical drawings, dimensions, and required specifications.</li><li>Use inspection tools including micrometers, calipers, and gages.</li><li>Communicate with operators on the production floor regarding non-conforming materials.</li><li>Assist with supplier change request forms, quality documentation, and processes such as FMEA and PPAP.</li><li>Utilize Excel for data collection and analysis.</li><li>Spend 50% of the time in the office handling quality documentation, reporting, and data analysis.</li><li>Spend 50% of the time on the floor reviewing product non-conformances, conducting defect analysis, and troubleshooting processes.</li><li>Maintain excellent communication and attention to detail.</li></ul> Essential Skills<ul><li>Experience in a regulated industry (medical, aerospace, automotive).</li><li>Understanding of technical drawings and specifications.</li><li>Proficiency with inspection tools such as micrometers, calipers, and gages.</li><li>Strong communication skills and attention to detail.</li></ul>Work EnvironmentThe work environment is an Electro-Mechanical Assembly setting, where you will split your time evenly between office work and floor activities. The role involves working closely with the operations team on either the 1st shift (7am – 3:30pm) or the 2nd shift (2pm – 10:30pm). The position is located in Buffalo Grove, IL, and offers a contract-to-hire opportunity. You will be part of a company that specializes in building products and electro-mechanical systems for other companies. This position requires a professional demeanor in a dynamic and collaborative environment.

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Technician</h1>Job DescriptionWe are seeking a dedicated Quality Technician to join our team. The ideal candidate will have an associate degree and 0-3+ years of experience working in a regulated industry such as medical, aerospace, or automotive. This role involves reviewing product non-conformances and completing quality documentation related to part defects and inspection plans. The successful candidate will have a solid understanding of technical drawings, dimensions, and required specifications, and the ability to use inspection tools such as micrometers, calipers, and gages. Responsibilities<ul><li>Review product non-conformances and complete quality documentation for part defects and inspection plans.</li><li>Understand and interpret technical drawings, dimensions, and required specifications.</li><li>Use inspection tools including micrometers, calipers, and gages.</li><li>Communicate with operators on the production floor regarding non-conforming materials.</li><li>Assist with supplier change request forms, quality documentation, and processes such as FMEA and PPAP.</li><li>Utilize Excel for data collection and analysis.</li><li>Spend 50% of the time in the office handling quality documentation, reporting, and data analysis.</li><li>Spend 50% of the time on the floor reviewing product non-conformances, conducting defect analysis, and troubleshooting processes.</li><li>Maintain excellent communication and attention to detail.</li></ul> Essential Skills<ul><li>Experience in a regulated industry (medical, aerospace, automotive).</li><li>Understanding of technical drawings and specifications.</li><li>Proficiency with inspection tools such as micrometers, calipers, and gages.</li><li>Strong communication skills and attention to detail.</li></ul>Work EnvironmentThe work environment is an Electro-Mechanical Assembly setting, where you will split your time evenly between office work and floor activities. The role involves working closely with the operations team on either the 1st shift (7am – 3:30pm) or the 2nd shift (2pm – 10:30pm). The position is located in Buffalo Grove, IL, and offers a contract-to-hire opportunity. You will be part of a company that specializes in building products and electro-mechanical systems for other companies. This position requires a professional demeanor in a dynamic and collaborative environment.

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Technician</h1>Job DescriptionThe primary function of this role is to assist with inspections, including receiving and in-process inspections, along with the associated paperwork such as reviewing, completing, and filing. Depending on the candidate&#39;s expertise, additional responsibilities may be offered, such as involvement in our Quality Management System with tasks like processing Non-Conformance Material Reports (NCMRs) or Change Requests, aligning with their strengths and career development goals. Responsibilities<ul><li>Conduct incoming, in-process, and final product inspections to ensure compliance with company and regulatory standards.</li><li>Support manufacturing processes by identifying and resolving quality issues in collaboration with production teams.</li><li>Manage the calibration of equipment and ensure tools and instruments are within specification and properly documented.</li><li>Oversee receiving inspection processes, ensuring that raw materials and components meet required quality standards before use in production.</li><li>Assist with investigating and documenting non-conformances, deviations, and corrective/preventive actions (CAPA).</li><li>Maintain accurate and detailed inspection records, calibration logs, and other quality-related documentation.</li><li>Collaborate with engineering and other cross-functional teams to support continuous improvement initiatives and ongoing projects.</li></ul> Essential Skills<ul><li>High school diploma or equivalent; technical certification or associate&#39;s degree preferred.</li><li>3+ years of experience as a Quality Technician in a regulated industry, preferably medical devices.</li><li>Experience with inspection techniques (e.g., visual, mechanical, dimensional) and the use of inspection tools (e.g., calipers, micrometers, CMM).</li><li>Familiarity with calibration processes and equipment management.</li><li>Strong attention to detail and ability to follow procedures and work instructions accurately.</li><li>Proficiency in Microsoft Office (Excel, Word, etc.) and experience with quality management software.</li><li>Excellent communication and documentation skills.</li></ul> Additional Skills &amp; Qualifications<ul><li>Problem-solving mindset with the ability to work in a fast-paced, dynamic environment.</li></ul> Work EnvironmentThis role requires working onsite every day. Job Type &amp; LocationThis is a Contract to Hire position based out of Saint Paul, Minnesota.

Quality Technician

Responsibilities<ul><li>Operate CMM machines to measure and inspect precision parts and components.</li><li>Interpret engineering drawings, blueprints, and GD&amp;T symbols.</li><li>Create and modify CMM programs using software such as PC-DMIS, Calypso, or MODUS.</li><li>Perform in-process and final inspections to ensure parts meet dimensional tolerances.</li><li>Perform first article inspections (FAI), PPAPs, and final part verifications.</li><li>Maintain and calibrate inspection equipment to ensure accuracy and compliance.</li><li>Follow company quality procedures, safety policies, and ISO standards.</li></ul> Essential Skills<ul><li>2+ years of experience operating and programming CMMs in a manufacturing environment.</li><li>Proficiency in CMM software such as PC-DMIS, Calypso, or similar.</li><li>Strong understanding of GD&amp;T and ability to interpret technical drawings.</li><li>Experience with ISO 9001.</li></ul>

<h1 style="font-size: 2em; font-weight: normal;">Quality Control Lab Technician</h1>shift available:6:00PM-2:30AM (2 openings) with $1.25/hr shift premium1:30AM -10:00 a.m. (1 opening) with $1.25/hr shift premium Job DescriptionThe QC Lab Technician will split their time equally between the plant floor and a lab setting. They will play a vital role in ensuring compliance with food safety standards and quality assurance protocols. Responsibilities<ul><li>Perform inspections including Pre-Operative and Food Safety, and document and communicate results.</li><li>Carry out Daily Operating Inspections to assure compliance with GMPs and USDA requirements.</li><li>Perform magnet and metal detector record checks and inform the supervisor of any deficiencies.</li><li>Conduct ATP swab tests with daily and weekly line swabs.</li><li>Calibrate lab scale, pH meter, and salt analyzer.</li><li>Conduct organic start-up tests ensuring no unauthorized cleaner was used and the line was triple rinsed, achieving a pH of 7.</li><li>Review previous day’s HACCP records daily.</li><li>Change thermometer recorder charts as needed.</li><li>Perform quality audits, including quality systems, production scales, and salt analyzers, and document and communicate results.</li><li>Perform inbound checks and verify COAs to ensure compliance with requirements.</li><li>Maintain stock of laboratory and production supplies as directed.</li><li>Act as a liaison with USDA.</li><li>Distribute weekly Code Date Sheets promptly.</li><li>Report and follow-up on food safety and food quality concerns.</li><li>Conduct pizza line coverage checks.</li><li>Notify the supervisor of all downtimes.</li><li>Enforce all Food Safety PPE/GMP requirements and report any concerns.</li><li>Perform other duties as assigned by the supervisor.</li></ul>Essential Skills<ul><li>Proficiency in quality checks and inspections, particularly in the food industry.</li><li>Understanding of GMP standards and compliance.</li><li>Knowledge of biology and chemistry, especially in a laboratory setting.</li><li>Quality assurance and quality control expertise.</li></ul>Additional Skills &amp; Qualifications<ul><li>High school diploma with science classes and/or lab courses, plus 6 months to 1+ years of manufacturing experience in the food industry.</li><li>Associate&#39;s degree in Life Sciences with 6 months to 1 year of manufacturing experience in the food industry.</li><li>6 months to 1+ years of GMP experience, open to environments like ISO and GLP.</li></ul>

<h1 style="font-size: 2em; font-weight: normal;">Quality Technician</h1>Shift: Monday - Friday from 6am -2:30pm | Offers Benefits | Long-Term Opportunity Job DescriptionWe are seeking a dedicated Quality Technician to join our team. In this role, you will ensure that material inspections comply with customer and regulatory requirements, promote a culture of continuous improvement, and perform additional assigned tasks. Our facility specializes in cosmetic and personal care manufacturing, offering a dynamic and challenging environment. Responsibilities<ul><li>Conduct evaluations of incoming materials to ensure alignment with defined standards and specifications.</li><li>Verify that final products and packaging meet predetermined quality benchmarks.</li><li>Adhere to established operational protocols, procedural guidelines, and testing frameworks.</li><li>Maintain accurate records of inspection outcomes and relevant data within designated tracking systems.</li><li>Identify and address deviations from quality expectations through formal escalation procedures.</li><li>Facilitate communication and sample/data exchange with external stakeholders when necessary.</li><li>Promote a culture of continuous improvement by identifying and eliminating inefficiencies.</li><li>Apply structured problem-solving tools to implement lasting enhancements.</li><li>Uphold organizational standards for cleanliness, order, and consistency across workspaces using a five-principle system.</li><li>Perform other work as assigned.</li></ul>Additional Skills &amp; Qualifications<ul><li>High School Diploma required</li><li>Experience or exposure to working within Quality</li><li>Bachelor&#39;s or Associate&#39;s degree in chemistry, biology, or a related science discipline is preferred</li><li>GMP experience from food, cosmetics, chemical manufacturing, pharma, or medical device sectors is a plus</li></ul>

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Technician</h1>Job DescriptionWe are seeking a detail-oriented Quality Technician to oversee the product review process from start to finish. This role involves significant involvement in the ramp-up for the snow season, requiring expertise in basic measurements using micrometers and calipers. Experience in Coordinate Measuring Machines (CMM) is advantageous. The technician will track the process starting from the fabrication shop, through the weld shop, to the final product, utilizing programs like Excel, SharePoint, and Minitab for documentation. The work will be evenly split between documentation and hands-on tasks. Responsibilities<ul><li>Review products throughout the production line from the fab shop to the final product.</li><li>Utilize micrometers and calipers for basic measurements.</li><li>Document processes using Excel, SharePoint, and Minitab.</li><li>Understand and apply different measurement scales and terminologies.</li><li>Perform measurement conversions and solve basic math problems.</li><li>Select appropriate measuring tools and techniques for specific characteristics.</li><li>Measure using surface plate layouts.</li><li>Collaborate with various departments to reduce waste and improve quality.</li></ul> Essential Skills<ul><li>Proficiency with calipers, micrometers, and quality control inspections.</li><li>Strong knowledge of basic mathematical operations.</li><li>Ability to perform measurement conversions and solve equations.</li><li>Capability to read and understand blueprints in detail.</li><li>Effective problem-solving and diagnostic skills.</li><li>Strong communication skills for cross-departmental collaboration.</li></ul> Additional Skills &amp; Qualifications<ul><li>Experience with CMM is a plus.</li><li>Quality certifications such as PPAP are advantageous.</li><li>Knowledge of quality methodologies like SPC, 8D, and 5 Whys is beneficial.</li></ul> Work EnvironmentThe position involves working across two different plants, including the fab shop and the manufacturing/assembly floor. The role requires working along inspection lines to ensure quality control while contributing to the company&#39;s efforts to reduce waste costs. The environment offers significant opportunities for growth as part of a dynamic quality team. Job Type &amp; LocationThis is a Contract to Hire position based out of Brillion, Wisconsin.

<h1>Job Title: Quality Technician</h1>Job DescriptionWe are seeking a skilled Quality Technician with experience in operating and programming Coordinate Measuring Machines (CMMs) in a manufacturing environment. The ideal candidate will have a strong knowledge in quality assurance and metrology, particularly within the aerospace, medical device, or automotive industries. Responsibilities<ul><li>Operate CMM machines to measure and inspect precision parts and components.</li><li>Interpret engineering drawings, blueprints, and GD&amp;T symbols.</li><li>Create and modify CMM programs using software such as PC-DMIS, Calypso, or MODUS.</li><li>Perform in-process and final inspections to ensure parts meet dimensional tolerances.</li><li>Document inspection results and maintain detailed records of measurements.</li><li>Collaborate with machinists, engineers, and quality personnel to resolve quality issues.</li><li>Perform first article inspections (FAI), PPAPs, and final part verifications.</li><li>Maintain and calibrate inspection equipment to ensure accuracy and compliance.</li><li>Follow company quality procedures, safety policies, and ISO standards.</li></ul> Essential Skills<ul><li>2+ years of experience operating and programming CMMs in a manufacturing environment.</li><li>Proficiency in CMM software such as PC-DMIS, Calypso, or similar.</li><li>Strong understanding of GD&amp;T and ability to interpret technical drawings.</li><li>Experience with ISO 9001 and/or AS9100 quality systems.</li><li>Excellent attention to detail and problem-solving skills.</li></ul> Additional Skills &amp; Qualifications<ul><li>High school diploma or equivalent; technical training or associate’s degree preferred.</li><li>Familiarity with other inspection tools such as micrometers, calipers, and height gauges.</li><li>Ability to work independently and as part of a team.</li></ul> Work EnvironmentThis position operates on the 2nd shift, from 2 PM to 11 PM. Enjoy incentives such as a 401K with 100% matching up to 6%, 100% tuition reimbursement for in-state accredited approved programs, and extremely affordable health, dental, and vision benefits. Additionally, participate in our Employee Stock Purchase Plan with a 15% discount on purchased stock at the lowest price of the quarter.

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Technician</h1>Job DescriptionThe Quality Technician is responsible for supporting quality-related functions, including incoming inspections, first articles, and managing customer returned products. The role involves inspecting incoming parts according to customer specifications or applicable blueprints, generating inspection reports, investigating returned products, and providing corrective action plans. Additionally, the role requires processing DMR information in Epicor and generating Certificates of Conformance for products. Responsibilities<ul><li>Support quality-related functions such as incoming inspection, first articles, and customer returned product management.</li><li>Inspect incoming parts according to customer specifications and applicable blueprints.</li><li>Generate accurate inspection reports.</li><li>Investigate returned (RMAs) products and provide corrective action plans to customers as required.</li><li>Process DMR information in Epicor.</li><li>Generate Certificates of Conformance for products when necessary.</li></ul> Essential Skills<ul><li>Proficiency in quality systems and blueprint reading.</li><li>Ability to conduct root cause analysis and implement corrective action plans.</li><li>Basic computer skills, including Microsoft Office.</li><li>Proficiency in using basic visual and mechanical inspection tools.</li><li>Familiarity with ISO Quality System Requirements.</li></ul> Additional Skills &amp; Qualifications<ul><li>High School Diploma or equivalent.</li><li>Knowledge of the AS9100 standard is a plus.</li></ul> Job Type &amp; LocationThis is a Contract position based out of Berlin, Wisconsin.

<h1>Job Title: Quality Technician</h1>Job DescriptionWe are seeking a detail-oriented Quality Technician to oversee the product review process from start to finish. This role involves significant involvement in the ramp-up for the snow season, requiring expertise in basic measurements using micrometers and calipers. Experience in Coordinate Measuring Machines (CMM) is advantageous. The technician will track the process starting from the fabrication shop, through the weld shop, to the final product, utilizing programs like Excel, SharePoint, and Minitab for documentation. The work will be evenly split between documentation and hands-on tasks. Responsibilities<ul><li>Review products throughout the production line from the fab shop to the final product.</li><li>Utilize micrometers and calipers for basic measurements.</li><li>Document processes using Excel, SharePoint, and Minitab.</li><li>Understand and apply different measurement scales and terminologies.</li><li>Perform measurement conversions and solve basic math problems.</li><li>Select appropriate measuring tools and techniques for specific characteristics.</li><li>Measure using surface plate layouts.</li><li>Collaborate with various departments to reduce waste and improve quality.</li></ul> Essential Skills<ul><li>Proficiency with calipers, micrometers, and quality control inspections.</li><li>Strong knowledge of basic mathematical operations.</li><li>Ability to perform measurement conversions and solve equations.</li><li>Capability to read and understand blueprints in detail.</li><li>Effective problem-solving and diagnostic skills.</li><li>Strong communication skills for cross-departmental collaboration.</li></ul> Additional Skills &amp; Qualifications<ul><li>Experience with CMM is a plus.</li><li>Quality certifications such as PPAP are advantageous.</li><li>Knowledge of quality methodologies like SPC, 8D, and 5 Whys is beneficial.</li></ul> Work EnvironmentThe position involves working across two different plants, including the fab shop and the manufacturing/assembly floor. The role requires working along inspection lines to ensure quality control while contributing to the company&#39;s efforts to reduce waste costs. The environment offers significant opportunities for growth as part of a dynamic quality team.

<h1>Job Title: Quality Technician</h1> Job DescriptionAs a Quality Technician, you will spend the majority of your time on the production floor performing quality checks, ensuring adherence to quality processes, and maintaining proper documentation. There is minimal opportunity for lab work, which involves preparing samples to be sent to a third-party testing partner. You will accurately interpret and follow reference documentation, including specifications and standard operating procedures (SOPs), while complying with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). Effective communication of quality-related information both verbally and in written form is essential. Responsibilities<ul><li>Perform quality checks on the production floor.</li><li>Ensure quality processes are followed.</li><li>Maintain and update documentation accurately.</li><li>Prepare samples for third-party testing.</li><li>Interpret and adhere to specifications and SOPs.</li><li>Comply with GMP and GLP standards.</li><li>Communicate quality-related information effectively.</li></ul>Essential Skills<ul><li>Quality control experience, preferably at least 6 months if no degree.</li><li>Associates degree in the sciences (no experience required).</li><li>Attention to detail and basic math skills.</li><li>Strong communication skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Interest in developing a career in manufacturing/quality settings.</li><li>Desire for upward mobility.</li></ul>Work EnvironmentThis position is located on the first shift from 9am-5:30pm / with training on 7:00 AM to 3:30 PM in a clean manufacturing environment. The facility is large, with several production lines where you will need to walk around and pull samples. The work environment is positive, with a strong company culture that values training and employee development.

<h3>Position: Quality Technician</h3>Location: Deland, FloridaPay Range: $25.00 – $31.25/hour<hr><h3>About the Role</h3>We’re looking for a detail-driven Quality Technician to join our team in Deland. In this role, you’ll help ensure our products meet rigorous quality standards and comply with ISO regulations. You’ll be hands-on with inspections, testing, and collaborating across teams to maintain excellence in our manufacturing processes.<hr><h3>Key Responsibilities</h3><ul><li>Conduct inspections and testing on incoming materials, in-process items, and finished goods.</li><li>Identify and document quality issues and non-conformances.</li><li>Maintain accurate records of inspections, test results, and corrective actions.</li><li>Work closely with production and engineering teams to resolve quality concerns.</li><li>Support the development and implementation of quality control procedures.</li><li>Ensure compliance with internal standards, customer requirements, and ISO 9000 regulations.</li></ul><hr><h3>Qualifications</h3><ul><li>High school diploma or equivalent required; associate degree or technical certification preferred.</li><li>1–3 years of experience in a manufacturing environment.</li><li>Familiarity with ISO 9000 standards.</li><li>Basic computer proficiency (Microsoft Office, data entry systems).</li><li>Knowledge of Lean Manufacturing is a plus.</li></ul><h1> </h1>

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Quality Technician 5_Non-Cleared</h1>Job DescriptionAs a Quality Technician, you will play a critical role in ensuring that our raw materials and finished products meet the highest standards of quality. You will be responsible for compliance with company standards, customer requirements, and applicable government regulations. Responsibilities<ul><li>Conduct inspections of raw materials and finished products to ensure compliance with quality standards.</li><li>Utilize GDT knowledge to create CMM inspection programs.</li><li>Support the CMM Programming team in ensuring product and process compliance by providing CMM Programming solutions.</li><li>Participate in the Material Review Board (MRB) process by screening for non-conformance.</li><li>Ensure implementation of measuring systems in line with GDT drawing interpretations.</li></ul> Essential Skills<ul><li>Bachelor&#39;s Degree with 3 or more years of experience in Quality and/or Manufacturing operations, or a High School/GED with 8 years of experience in a similar environment.</li><li>Expert knowledge in GDT drawing interpretation.</li><li>Experience in inspecting parts for conformance using mechanical inspection tools such as microscopes, micrometers, calipers, gauges, and indicators.</li></ul> Additional Skills &amp; Qualifications<ul><li>CMM programming experience with Zeiss machines.</li><li>Experience in manufacturing or quality in the aerospace industry.</li><li>Knowledge of aerospace industry quality standards and procedures.</li><li>Advanced knowledge of ASME Y 14.5-1994 and ASME Y 14.5-2018.</li><li>Excellent priority management skills.</li></ul> Work EnvironmentYou will work in an environment that emphasizes quality and precision. The role involves handling advanced technologies such as CMM machines and requires familiarity with mechanical inspection tools. The position is ideal for those who thrive in a structured, regulated environment where attention to detail and adherence to standards are paramount. Job Type &amp; LocationThis is a Contract position based out of Mountainhome, Pennsylvania.

<h1 style="font-size: 2em; font-weight: normal;">Quality Technician</h1> Job DescriptionWe are seeking a Quality Technician to join a team dedicated to designing, developing, and marketing advanced wound healing technologies within the medical device industry. This role involves working collaboratively with Operations, Quality, and Engineering teams. Responsibilities<ul><li>Conduct 25% of activities in receiving inspection.</li><li>Support various quality functions such as QMS documentation, CAPA support, and validation activities, covering 75% of responsibilities.</li><li>Prepare engineering and test samples.</li><li>Receive and inspect incoming raw materials.</li><li>Record test results and compare them to acceptance criteria.</li><li>Print and verify finished product labeling.</li><li>Review and approve product lot folders.</li><li>Support equipment installation and qualification activities.</li><li>Assist in developing internal and supplier-based quality plans.</li></ul>Essential Skills<ul><li>Proficiency in using measurement tools like Micrometers and Calipers.</li><li>Experience with QMS documentation.</li><li>Minimum of 2 years of experience in a Quality Technician role, preferably in the medical device industry.</li><li>Strong documentation skills.</li><li>Self-starter mentality with the ability to manage multiple tasks.</li></ul>Additional Skills &amp; Qualifications<ul><li>Preferred 2-year degree.</li><li>Experience in quality testing, medical device documentation, and CAPA.</li><li>Capability to support labeling activities.</li></ul>

Description
					This position is assisting daily production, work on continuous improvement on the shop floor, managing the SCAR (supplier NCR) and the NCR linked to his/her scope of activities, assuring compliance to and providing guidance regarding interpreting ISO 13485 &amp; FDA standards in link with the Manufacturing Quality activities. The Manufacturing QA Technician is working with the Manufacturing QEs and the Quality inspectors (QAR).
					Skills
					quality assurance, blueprint reading, gd&amp;t, Inspection, Quality control, Quality inspection, Blueprint, Visual inspection, qc analysis, erp system, technical writing, solidworks
					Top Skills Details
					quality assurance,blueprint reading,gd&amp;t
					Additional Skills &amp; Qualifications
					Preferred Qualifications:	
- Experience in an ISO 13485:2016 certified system.
- Understanding of manufacturing processes, equipment, fixturing, and tooling.
- Advanced knowledge of inspection equipment and maintenance.
- Experience in Calypso
- Experience in 2D and 3D CAD (Solidworks)
					Experience Level
					Entry Level

<h1 style="text-align: center;">Quality Technician</h1>Job DescriptionThis position is responsible for monitoring the food safety and quality of products and services to ensure they meet all customer and regulatory standards by utilizing quality tools and systems application. Responsibilities<ul><li>Perform all required product and batch inspection responsibilities.</li><li>Maintain work areas and equipment within GMP and GLP standards.</li><li>Place non-conforming raw materials, packaging, and finished products on hold as required.</li><li>Perform required analytical and microbiological testing as defined by Food Safety and Quality systems.</li><li>Verify product codes and chart recorders.</li><li>Perform microbiological activities including but not limited to ATP swabs, culture swabs, plating, BacT/Alert3D, and 3M film plating as required by the facility.</li><li>Monitor thermal process checks including pasteurizer temperatures and packaging sterilization processes.</li><li>Participate in GMP, GLP, Food Safety, and Food Quality programs.</li><li>Ensure measurement accuracy by keeping lab equipment in calibration and in operating order through preventative maintenance and troubleshooting.</li><li>Perform analytical testing on products, water, raw materials, ingredients, packaging, etc.</li><li>Analyze, interpret, and utilize statistical process control data to make informed decisions.</li><li>Perform 24-hour sensory evaluation of products in the lab.</li><li>Participate in internal inspections and audits.</li><li>Maintain accurate paperwork and records to meet all government and company requirements, both physical and electronic.</li><li>Communicate quality, food safety, and compliance concerns immediately for prompt resolution.</li><li>Communicate quality results and collaborate with cross-functional departments to resolve issues timely.</li><li>Collect samples for retention and customer use.</li><li>Organize and maintain the sample storage and retain area.</li></ul> Essential Skills<ul><li>High School Diploma or GED.</li><li>Ability to wear personal protective equipment such as a bump cap, hair net, ear plugs, beard net (if applicable), Kevlar gloves, safety glasses, and leather skid-resistant work shoes/boots.</li><li>Ability to apply intermediate computer and communication skills, math functions, and reasoning.</li><li>Ability to use tools/gauges such as refractometer, salt titrator, acid titrator, PH meter, color meter, moisture meter, and consistometer.</li><li>Self-motivated with the ability to work independently.</li></ul> Additional Skills &amp; Qualifications<ul><li>Previous experience in quality control is preferred.</li></ul> Work EnvironmentThe work environment involves extended standing and frequent moving by foot. There is exposure to extreme loud noises and extreme hot/cold (non-weather) environments. The role requires lifting/carrying less than 30 pounds, reaching, and use of fingers. The position may involve working in high places and near moving mechanical parts, frequent reaching/pulling/bending/climbing stairs/stooping/kneeling/bending, and frequent lifting of over 30 pounds or pushing 80 pounds on a cart. There is potential exposure to caustic substances. Job Type &amp; LocationThis is a Permanent position based out of Rochester, New York.

If interested, email wdavy @ Actalentservices.com or call 330 685 3145 Description•	Execute Quality Monitoring Scheme routines across all manufacturing processes, including batching, processing, filling, and packaging.•	Execute physical and chemical testing of raw batches, finished products and any other testing as defined by the Quality Monitoring Scheme.•	Execute postproduction testing, including Microbiological testing on quarantine samples.•	Execute pre-operation routines, which includes sanitation approval for equipment and environment, and compliance against product change-over requirements.•	Execute CIP validation utilizing allergen swabs.•	Coordinate collection and storage of finished product samples during manufacturing operation.•	Execute hold routines including creating events for nonconforming ingredients, packaging material, raw batches, and finished products.•	Execute review and approval of food safety and quality records created throughout shift.•	Execute verification routines for Pre-Requisite records and Programs.•	Provide contribution towards root cause analysis and customer complaint investigations.•	Provide contribution towards maintenance and improvement of FSQ documentation practices.•	Scan/file records as needed.•	Maintain organization, cleanliness, and housekeeping of FSQ Lab area.•	Other duties, as assigned by management.Skillslaboratory, aseptic, food and beverageTop Skills Detailslaboratory,aseptic,food and beverageAdditional Skills &amp; Qualifications•	High school diploma or equivalent.•	Ability to communicate effectively written and verbally.•	Ability to document, describe and interpret records and documented specifications.•	Ability to enforce company procedures and policies.•	Ability to document inspection findings legibly and with accuracy.•	Ability to perform basic math calculations. preferred •	BS in Food Science, Food Engineering or equivalent.•	At least 1 year of experience in a QA function within food or beverage manufacturing industry.•	Work experience and trained in HACCP.Experience LevelEntry Level

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