- Randstad US (Norwood, MA)
- quality assurance specialist - gmp - hybrid. + norwood , massachusetts + posted may 9, 2024 **job details** summary + $55 - $56 per hour + temporary + ... What You'll Need: + 3+ years of experience in a GMP Manufacturing environment, focused on Quality Assurance + Bachelor's degree in a science related field +… more
- Bausch Health (Petaluma, CA)
- …of improving peoples lives with our health care products. Join our team as a ** Quality Assurance Specialist , GMP ** at our _Petaluma site_ ! We're seeking ... in analytical lab equipment operation. + Review and approve various GMP documents including batch records, specifications, test methods, and validation reports.… more
- Regeneron Pharmaceuticals (Troy, NY)
- We are currently looking to fill a Quality Assurance Specialist ( GMP Auditing) position. This position will support the GMP Auditing department by ... Prepares written audit documents and reports and ensures the quality and accuracy of all audit documentation. + Identifies...extensions are initiated and processed. + Writes and launches GMP audit CAPAs. + Prepares and presents metrics to… more
- Seattle Children's (Seattle, WA)
- Responsibilities: The GMP Quality Assurance Document Control (QADC) Specialist will primarily be responsible for the Therapeutic Cell Production Core GMP ... management and filing of controlled documents, and retention of GMP records. The QADC Specialist is responsible...paper and electronic systems. The GMP QADC Specialist will work closely with Quality Assurance… more
- Seattle Children's (Seattle, WA)
- …+ Minimum one (1) years academic, biotechnological, or pharmaceutical industry Quality Assurance experience in a GMP biologics manufacturing environment. ... of Seattle Children's Therapeutics with development, implementation, and maintenance of quality assurance systems and activities. Assist with internal audits, assist… more
- United Therapeutics (Eden Prairie, MN)
- …to help patients with liver and kidney disease. How you'll contribute The Quality Assurance Specialist II ensures that all intermediates and products ... the Miromatrix are manufactured in accordance with current Good Manufacturing Practices ( GMP ) and meet all internal specifications. This position will support the… more
- Editas Medicine (Cambridge, MA)
- …Position Summary Editas is seeking a cooperative, highly motivated and experienced quality professional to support internal GMP manufacturing operations. This ... Waltham and Devens GMP manufacturing facilities as a member of the Quality Operations team. Specific responsibilities include but are not limited to Quality … more
- Cambridge Isotope Laboratories, Inc. (Andover, MA)
- …of the Quality Specialist is to maintain the adherence to quality standards for non- GMP products. Responsibilities + Develop, implement, and maintain an ... Cambridge Isotope Laboratories, Inc. (CIL) is searching for an ISO Quality Specialist based onsite in our Andover, MA facility. CIL is the global leading company… more
- Boehringer Ingelheim (St. Joseph, MO)
- …reflect Boehringer Ingelheim's high regard for our employees. The Principal Specialist , Validation manages all phases of higher level, more complex validation ... requirements and are suitable for their intended purposes. The Principal Specialist , Validation will lead project management efforts for validation activities… more
- Bristol Myers Squibb (Bothell, WA)
- …patients, there's no better place than here at BMS with our Cell Therapy team. The Quality Assurance Specialist position plays a key role in supporting the cGMP ... quality operations for the Bothell Manufacturing Plant (Jump). Primary...regulated cGMP environment. The primary focus of the QA Specialist role will be to support routine clinical and… more
- ThermoFisher Scientific (Franklin, MA)
- …Impactful Work:** The QA/QC Specialist is responsible for driving the day-to-day GMP Quality Control and Quality Assurance activities for the Franklin ... level compliance. This position supports the continued development of GMP capability and maintenance of compliance to US FDA... capability and maintenance of compliance to US FDA Quality System Regulations and performs site level Quality… more
- Editas Medicine (Devens, MA)
- …Position Summary Editas is seeking a cooperative, highly motivated and experienced quality professional to support internal GMP manufacturing operations. This ... Waltham and Devens GMP manufacturing facilities as a member of the Quality Operations team. Specific responsibilities include but are not limited to Quality … more
- Merck (Rahway, NJ)
- …a high degree of technical and project management responsibility. The Specialist -Engineering position will report to the Associate Director, Engineering and ... new chemistries, and exploring new technologies. **Responsibilities of the Specialist - Engineer include the following:** The engineer role...and equipment in the facility are ready for the GMP and non- GMP work that the scientists… more
- System One (Bothell, WA)
- Job Title: Quality Assurance Specialist Location: Bothell, WA Hours/Schedule: 9:00pm - 7:30am, Sun - Wed Compensation: $37.00 - $42.41/hr Type: Contract, ... and resolve discrepancies with manufacturing operators or supervisors. + Provide Quality on-the-floor oversight including quality walk-throughs of the… more
- Randstad US (Norwood, MA)
- sr. specialist quality assurance. + norwood ,...field. + 7 - 10 years' experience within a Quality role at a GMP manufacturing environment ... work hours: 9 to 5 education: Bachelors responsibilities: The Quality Assurance Sr. Specialist is based in...company that is Bold, Relentless, Curious, and Collaborative. skills: Quality control, SOP, MS-WORD, MS-EXCEL, MS-Powerpoint, GMP … more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …our mission! Kite is seeking a highly motivated individual to join Kite as a QC Specialist III, Global Quality Control, to provide Quality Control support of ... of raw material and reagents, within a Good Manufacturing Practices ( GMP ) environment. **Responsibilities:** + Independently performs routine Raw Materials release… more
- BioFire Diagnostics, LLC. (Hazelwood, MO)
- Position Summary: The Quality Inspection Specialist is responsible for performing physical inspection of card batches on the production floor, supports ... quality walkthroughs of production areas and changeovers between batches...GED with minimum 6 years applicable experience in a GMP environment OR + Associates degree with 4+ years… more
- Unither Pharmaceuticals (Rochester, NY)
- Quality Specialist - Development & Validation... will review and approve a wide variety of GMP related documents and will serve as an internal ... more than 280 employees. Your role Reporting to the Quality Assurance Manager, The Quality Specialist...as media fill tests. May be required to provide GMP training to new hires. Facilitates cross functional building… more
- Cambridge Isotope Laboratories, Inc. (Tewksbury, MA)
- Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Documentation Specialist based onsite in our Andover, MA facility. CIL is the ... has had consistent growth for over 40 years. The Quality Control Documentation Specialist is responsible for...purpose. Responsibilities + Review batch data for release of GMP /ISO and/or non-regulated materials by ensuring the product meets… more
- Amgen (Thousand Oaks, CA)
- …your best work alongside other innovative, driven professionals in this meaningful role. ** Specialist Quality Assurance** **Live** **What you will do** Let's do ... and transportation service providers **Typical tasks include:** + Internal Quality Assurance support for GMP warehouse and...include:** + Internal Quality Assurance support for GMP warehouse and inventory management operations + External … more