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Regularly report studio QMS implementation and audit resolution strategies to the Managing Principal and Regional Quality Director. Serve as the local representative within the studio for the Quality Office and support the development and implementation of the organizations Quality Management System (QMS.
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The Quality Assurance Specialist II supports the day-to-day quality operations via Manufacturing Clean Room presence, Material/Inventory QA Release, oversight of all elements of the Quality Management System (QMS), including but not limited to deviations, Corrective and Preventive Actions (CAPAs), change control, batch review, data integrity, and training in support of biologics manufacturing production.
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The position requires significant cross-functional coordination between Controls, Mechanical, Electrical, Firmware and Quality teams. Statistical Quality Control. Interact with Mechanical, Electrical, Firmware and Controls teams to build reliability and validation test infrastructure.
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A career at Ironwood Pharmaceuticals means you’ll be part of something genuinely special.
Full-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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CPA firm seeking Quality Control Manager for our Non-Profit practice. Participate in due diligence projects to assess audit quality, effectiveness and efficiency of existing engagements and/or or potential firm merger candidates.
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BS in a scientific or engineering discipline with minimum of 8 years of experience in Quality Assurance, Quality Control, or a GMP related field within a biotechnology, biologics, or pharmaceutical manufacturing facility, with at least 2 years conducting internal and external audits.
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This person will partner with (1) the Product Teams to drive high quality product delivery, (2) the QA Manual Testing and Requirements Team to synchronize virtual and physical tests, and (3) the internal Customers (Operations, Maintenance, Process, Ops Engineering, etc.
$201,200 a yearFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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The Air Quality Project Manager will work with the APCC and other City agencies, residents, businesses, and institutions to administer programs, identify obstacles, and facilitate solutions leading to short-term and long-term air quality improvements in support of the Mayor’s goals of carbon neutrality and a healthy environment.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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DPS Group is seeking a qualified Senior Quality Assurance Operations professional to perform batch disposition, batch record review, deviation, CAPA and change control support at the Boston, MA client site.
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The Breast Imaging Quality Navigator is responsible for maintaining the highest levels of empathy, communication, and efficiency to provide exemplary patient guidance and direction through complex imaging and treatment pathways.
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Quality Control analyst will interact regularly with Quality Assurance, Analytical Development, Manufacturing, Facilities, as well as external test laboratories. 3+years of experience in Quality Control in GMP environment.
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Reporting to the Director, R&D GLP/GCLP Quality, located at the Moderna Headquarters in Cambridge, MA, the Manager of Good Laboratory Practice/Good Clinical Laboratory Practice (GLP/GCLP), applies established knowledge and experience in internal, in-process, study and vendor audits.
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Build and maintain the Quality processes needed to support Quality oversight of Technical Operations deliverables, including but not limited to supplier management, tech transfer, production (master cell bank, drug substance, drug product, combination products, etc.
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As a Senior Field Quality Engineer, you will work closely with WHOOP Manufacturing, Supply Chain & Operations, Hardware Engineering, and Membership Services teams as you will be responsible for field quality, triage on high customer impact returns, and RMA processes/metrics.
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For this position, you must reside in within commuting distance to our Ultrasound sites in Bothell, WA, Cambridge, MA or Reedsville, PA.You're the right fit if: You’ve acquired a minimum of 10 years’ experience working in FDA regulated medical device quality, with a focus in Design Quality Engineering in support of the development and introduction of new products and sustaining releases.
$236,000 a yearFull-timeExpandApply NowActive JobUpdated Today
Title: quality Company: Proactive Strategies in Waltham, MA
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