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Contact: John@SourceRecruitmentSolutions.com Our client, a premier Food Manufacturing Company with products sold nation wide is seeking an experienced Quality Assurance Manager. 5+ Years Quality Assurance experience in a Food Production Manufacturing plant.
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The role of Manager, Clinical Quality Assurance, supports Quality oversight for Bicycle’s development programs, ensuring compliance with applicable GLP and GCP standards and global regulations.
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The QA/QC Manager, a pivotal role in our organization, will be responsible for quality control, quality assurance, quality management, and Good Manufacturing Practice (GMP.
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Proficiency in using various software and databases for quality assurance and regulatory affairs Benefits: We are a values-driven, creative team, and we know that we’re only successful because of the talented people on our team.
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About the JobThe Senior Manager, Manufacturing Quality Engineering in the Quality Assurance department is a key and critical role at FMI. This role presents the incumbent with an opportunity to lead various teams within FMI. The Senior Manager is responsible for oversight and management of the Quality Assurance manufacturing team in Boston, MA with a global mindset ensuring continuity across all manufacturing sites.
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General knowledge of Purchasing, Quality Assurance, Manufacturing, Inventory Record Accuracy, Cycle Counting Procedures, Inventory Control Procedures, Food Safety Requirements, Warehousing and Distribution.
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The ideal candidate will have experience in the biotech or medical device industry and a strong background in process engineering, quality assurance, and production optimization. As a Manufacturing Engineer on the team, you will posses a passion for optimizing manufacturing processes, ensuring product quality, and driving continuous improvement.
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Interface with Quality Control and Quality Assurance teams to ensure compliant tech transfer activities are ongoing. Assist in developing and implementing strategies for continuous improvement across manufacturing processes that reduce cost, save time, improve process attributes, and optimize quality.
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Work closely with DTE Compliance, Internal Audit, and Quality Assurance groups as needed to ensure compliance with all appropriate regulations, as well as our DTE system lifecycle and change management requirements.
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Works in close collaboration with the Project Management and CMC teams and related functions, including discovery, non-clinical development, formulation development, analytical development, Quality Assurance and CMC Regulatory affairs.
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The Sr. Director, Quality Assurance will be responsible for implementing GxP (GCP/GLP/GMP) compliant Quality Management Systems, performing all required functions of the Quality Unit (ie product release) and building a Quality Assurance organization that fosters a strong Quality culture at Be Bio. This position will partner equally with both internal and external stakeholders and partners (CROs, CDMOs.
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This position works closely with key stake holders including Clinical Operations, Global Planning, Quality Assurance, Regulatory Affairs, Contract Manufacturing Operations (CMO’s), and Contract Research Operations (CRO’s) to ensure seamless supply of Clinical Trial Material.
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Effectively manage project risks, specifically those intrinsic to the offshore wind industry, manufacturing, Quality Assurance/Quality Control, and supply chain challenges.
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As the Sr. Director of GMP Quality Assurance, you will be responsible for providing quality oversight for Oruka’s clinical development programs and manufacturing. Advanced degree in a scientific field with a minimum of 12 years of experience in GMP Quality or Manufacturing in a biotechnology or pharmaceutical setting; experience in biologics is required.
$260,000 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Collaborate with cross-functional teams, including the CDMO joint project team, Abata Process and Analytical Development, Quality Assurance, Quality Control, and Regulatory to ensure the efficient execution of clinical manufacturing operations and the transfer of new assets and process enhancements within agreed timelines to support business objectives.
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quality assurance manufacturing jobs in Hyde Park, MA
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