QC Manager
Hired by Matrix
QC Manager
Are you ready to build your career by joining a certified technology solutions and compliance consulting services company? If so, our client is hiring a QC Manager. Position Type: Contract On-Site Required: 5 to 10 years of experience in Quality Control within pharmaceutical, biotech, or CDMO environments. Previous experience as QC Manager, QC Supervisor, QC Lead, or senior QC professional. Experience with GMP laboratory operations, documentation review, sample management, and product release support. Background in sterile drug product, biologics, aseptic manufacturing, or formulation development would be preferred. Good understanding of analytical testing and/or microbiology testing. Strong knowledge of GMP, FDA expectations, laboratory controls, and data integrity principles. Ability to work independently and manage priorities in a fast-paced environment. Strong communication and cross-functional collaboration skills. Bachelor's degree in Chemistry, Biology, Microbiology, Pharmaceutical Sciences, or related field.
Responsibilities: Supporting and managing daily QC laboratory operations, ensuring testing activities are completed on time and in compliance with internal procedures, client requirements, and applicable GMP regulations.
Key Responsibilities: Manage daily QC laboratory operations and support testing priorities. Oversee analytical and/or microbiology testing activities, depending on site needs. Support raw material, in-process, finished product, and stability testing processes. Review and approve QC documentation, test results, protocols, reports, and SOPs. Ensure compliance with cGMP, FDA requirements, internal procedures, and client expectations. Coordinate QC activities with Manufacturing, QA, Validation, Supply Chain, and Project teams. Support product release timelines from a QC perspective. Maintain inspection readiness within the QC area. Identify operational gaps and support process improvements within the laboratory. Provide guidance to QC team members and support workload prioritization.
$94k - $135k
...role, you will supervise a team of Document Control Specialists, manage escalations, and serve as the primary liaison between the quality... ...Quality Audits & Document Control OversightConduct and supervise QA/QC audits of POR Document Control files and electronic document...SuggestedFull timeWork at office$30 - $37 per hour
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- ...issues. You'll drive manufacturing quality improvements using 8D corrective action methodology, support our ISO 9001:2015 Quality Management System, and keep production running at the highest standards. What you'll do:Develop and implement quality standards; monitor and...SuggestedPermanent employmentLocal areaWorldwideMonday to FridayFlexible hours
$72k - $100k
...Conduct internal audits and support external customer and certification audits.Assist in maintaining compliance with ISO 9001 quality management system requirements.Maintain quality procedures, records, forms, risk assessments, and calibration programs.Provide guidance...SuggestedPermanent employmentFull time- ...and GMP procedures accurately Ability to work independently and manage routine laboratory tasks with minimal supervision Comfortable performing... ...simultaneously at least 1–2 years of laboratory experience. (GMP QC laboratory or pharmaceutical industry experience preferred)...
$23 - $27 per hour
...equipment as needed Lead, train, and direct team members Assign work and monitor productivity Participate in meetings with management regarding department performance Establish performance expectations and support employee development Prioritize testing...Hourly payFull timeTemporary workLocal areaMonday to FridayDay shiftAfternoon shift- #Eng-IT-01 Job Summary We are seeking an experienced Compliance Engineer to join our development team. The ideal candidate will assist in the design, testing, and certification of our electronic products, ensuring they meet agency compliance criteria, including ...Work experience placementLocal areaFlexible hours
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$30 - $40 per hour
...Ability to determine the proper inspection methods and measuring tools for various part features. ~ Working knowledge of quality management systems and standards, particularly ISO 9001 and AS9100. ~ Strong communication and interpersonal skills with the ability to...Full timeLocal areaAfternoon shift- ...nonconformance reports (NCR) for all non-conforming material identified throughout operations. Prepare and submit metrics reports to the QC Supervisor or Lead. Comply with all safety requirements ensuring work areas meet standards. Review and release job order...Local area
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...operations of the quality assurance team, ensuring that the company's products meet established quality standards. They implement and manage QA systems, coordinate audits, and lead initiatives to address and prevent quality issues.Responsibilities:Partner with our...Full timeRemote workFlexible hoursShift workDay shiftAfternoon shift- Job Title: MCS Senior Associate Quality Assurance Location: Thousand Oaks, California (On-site) Job Summary: We are seeking a dedicated professional to deliver real-time, floor-based quality assurance support within a leading drug substance production facility. Our team...Work experience placementDay shiftAfternoon shift
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$75k - $85k
...to validate new designs and support certification testing.Analyze and troubleshoot hardware/software issues; document findings and manage the end-to-end defect reporting lifecycle.Log and debug devices using various wireless protocols, including Z-Wave, Matter, 4G/5G LTE...Full timeWork experience placementWork at office- ...data analysis to identify trends and drive decisions.Effective communicator with the ability to collaborate cross?functionally and manage multiple priorities in fast?paced production and program settings.Six Sigma Green Belt (minimum) or Black Belt preferred, with experience...Minimum wageWork experience placementLocal area
$186k - $230k
...responsibilities include leading the site Quality organization (QA & QC) by providing leadership and guidance in quality decision making... ...global cross contamination control requirements • Support plant management groups on new products, changes to products, processes, and...Contract work$22 - $25 per hour
...oriented quality professional with aerospace manufacturing experience and a strong background supporting ISO 9001 and AS9100D quality management systems. The Quality Assurance Inspector will play a key role in ensuring products, processes, and documentation meet customer...Hourly payTemporary workMonday to Friday- ...ensuring products and processes meet established quality standards while supporting compliance with ISO 9001 and AS9100D quality management systems. The ideal candidate has a strong aerospace manufacturing background, excellent attention to detail, and a passion for maintaining...Work at officeImmediate start
$140.12k - $189.58k
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$67 - $77 per hour
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...environments. Monitor and trend process data to proactively identify opportunities for improvement. Team Leadership Responsible for managing and directing a global team of manufacturing scientists, technical transfer specialists, and process improvement engineers Lead...Full timeTemporary workWork experience placementWork at officeLocal area
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