- Randstad US (Norwood, MA)
- quality assurance specialist - gmp . + norwood , massachusetts + posted may 9, 2024 **job details** summary + $55 - $59 per hour + temp to perm + bachelor ... drug products produced at this facility. He/she will provide quality oversight and expertise to enable technical success with...You'll Need: + 2-4 years of experience in a GMP Manufacturing environment + Bachelor's degree in a science… 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)
- …+ 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
- Novo Nordisk (Clayton, NC)
- …+ Minimum of three (3) years progressively responsible experience in material management &/or GMP quality , required + Experience in one or more of the following ... At Novo Nordisk, we are helping to improve the quality of life for millions of people worldwide. For...regulated industry + API & raw materials + Regulations GMP &/or ISO + Pharmaceutical or other FDA regulated… more
- MD Anderson Cancer Center (Houston, TX)
- …(ESPs), and More than minimally manipulated manufacturing procedure within the GMP facility following standard policies and procedures which include but not ... one (maximum of two for certain procedures) Cell Therapy Specialist who is responsible for the entire process on...CLIA. Document deviations and events, notify supervisor, technical and quality management personnel in timely manner and assist in… more
- Mayo Clinic (Jacksonville, FL)
- …able to independently schedule workday activities with minimal direction. ASQ certification in quality and/or GMP principles (eg, quality process analyst, ... the resources you need to succeed. **Responsibilities** The Sr. Quality Analyst, FDA Regulated Manufacturing will be part of...four, consisting of the site QA manager, one QA specialist and two senior QA specialists. + Is responsible… more
- WuXi AppTec (Philadelphia, PA)
- …local work instructions and in conformance with client expectations and GMP quality standards. The Inventory Control Specialist will also be responsible for ... Medical, dental and vision insurance + and much more The **Inventory Control Specialist ** is responsible for maintaining a high level of inventory accuracy and… 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
- 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
- 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
- Bristol Myers Squibb (Indianapolis, IN)
- …their personal lives. Read more: careers.bms.com/working-with-us . **Position** : Quality Systems Associate/ Specialist **Location** : Indianapolis, Indiana ... aims to be the global leader in radiopharmaceuticals. The Quality Systems Associate/ Specialist will help support the...a Science related discipline preferred + 3-5 years of quality assurance experience + Pharmaceutical and GMP … more
- BioFire Diagnostics, LLC. (Hazelwood, MO)
- Position Summary: The Quality Specialist is responsible for lot related oversight for batch record completion. This includes MES and paper documentation ... WHYS, 5M+E, Is/Is Not, etc.), as applicable. + Authors and reviews GMP documents including procedure revisions and specified reports, to support continuous… more
- Merck (Rahway, NJ)
- …a high degree of technical and project management responsibility. The Specialist - Process/Facility Engineering position will report to the Director, Engineering ... production, utility systems and associated infrastructure. Responsibilities of the Specialist - Process/Facility Engineer include the following: The process engineer… 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
- 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
- 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
- Merck (Millsboro, DE)
- …supply to customers and patients on time, every time, across the globe. The Quality Control (QC) Associate Specialist , with Guidance from the QC Manager, ensures ... product/process quality through the review of GMP documentation...release of antigen and seed batches. The QC associate specialist must adhere to regulatory and site policies and… more
- Lilly (Durham, NC)
- …parenteral facility using isolator technology and a fully automated visual inspection. The Quality Assurance Floor Support Specialist works as a member of the ... semi- automated inspection, and manual inspection. QA Floor Support Specialist oversees visual inspection production functions to achieve patient...on quality matters, while driving the site Quality culture. + Reviews and approves GMP … more
- Amgen (Thousand Oaks, CA)
- …management when appropriate. + Reviewing protocols for manufacturing activities. + Liaising with Quality Assurance to ensure that GMP standards are maintained in ... Become the professional you are meant to be in this meaningful role. ** Specialist Manufacturing, New Product Introductions** **Live** **What you will do** Let's do… more
- Lilly (Concord, NC)
- …environment. This is an opportunity you don't want to miss! Responsibilities: The Quality Assurance Floor Support Specialist is responsible for providing QA ... and qualification of the Concord site. The QA Floor Support Specialist will demonstrate teamwork by collaborating cross functionally with various levels… more