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The Site Head also has responsibility for the Quality Management System (QMS) and product disposition of products to support customers clinical trials. Kincell is a technology-forward contract development and manufacturing organization (CDMO) that streamlines analytical development, process development, CMC consulting and early-stage GMP cell therapy manufacturing.
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Ensure labeling compliance with quality management system (QMS), regulatory requirements and guidelines, standard operating procedures, and work instructions. Exactech is a global medical device company that develops and markets orthopaedic implant devices, related surgical instruments and the Active Intelligence® platform of smart technologies to hospitals and physicians.
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You have strong experience writing and maintaining QMS processes- preferred. We are a health technology company. You acquired a minimum of 5 years’ experience in regulatory affairs within the FDA regulated, global medical device industry.
$104,000 - $178,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Understand and respect the QMS interfaces with the processes in whom it interacts. Set's serialization of Engineering Change Request based on CCB analysis of inventory levels, cost, and lead-time for planning, tooling, and sourcing.
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Responsible for complying with corporate-level and office-specific Quality Management Systems (QMS) related policies and procedures; including adoption, implementation and enforcement. The focus of this position will be on Laboratory Management, you may occasionally perform technician job duties.
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