- University of Southern California (Los Angeles, CA)
- …(https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP -Process-Development- Specialist \_REQ20145450/apply) ... for internal/external users in the university's current Good Manufacturing Practices ( cGMP ) facility. The Process Development Specialist is responsible for… more
- Danaher Corporation (Coralville, IA)
- …Our work is complex and cutting-edge, and our team members are curious, creative thinkers who understand that good data drives smart decisions. At IDT, we realize ... that although science may be uniform, people are unique. We promote a culture where engaged people are motivated and have opportunities to achieve their full potential, as part of one global team.IDT is one of 10 Life Sciences companies of Danaher. Together,… more
- University of Southern California (Los Angeles, CA)
- …students and staff that make the university what it is. The Senior QC Specialist at the USC/CHLA cGMP Facility will lead advanced quality control activities ... cGMP Senior Quality Control (QC) SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/Senior- cGMP… more
- Cardinal Health (Fort Lauderdale, FL)
- …improved disease diagnosis, staging, and monitoring. **_Job Summary_** The Senior Specialist , Quality Assurance role will support, Nuclear Manufacturing. This is ... at the PET manufacturing site, such as: + Handles cGMP documentation review related to product release, facilities and...products to meet the requirements of 21 CFR 212 ( cGMP ). + Handles and ensures quality of documentation (control,… more
- Cardinal Health (Louisville, KY)
- …reviewed for quality and documented. **_Job Summary_** The quality assurance specialist (QAS) performs all quality review and approval/release decisions at an ... used for Positron Emission Tomography (PET) scans. **_Responsibilities_** + Handles CGMP documentation review related to product release, facilities and equipment,… more
- Catalent Pharma Solutions (Hanover, MD)
- **Sr. Specialist , QA - Batch Disposition** **Summary:** _Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the ... and FDA approved facility, at approximately 200,000 sq. ft., houses 10 CGMP manufacturing suites, fill/finish, central services, testing labs, and a warehouse._ _The… more
- Merck (Durham, NC)
- **Job Description** We are seeking a Growth and Improvement minded Validation Specialist that can help drive our Strategic Operating Priorities. + Invent | Pursue ... a Competitive Advantage for Us **Summary, Focus and Purpose** The Validation Specialist will be an energetic, technical contributor and leader with strong… more
- Stanford University (Stanford, CA)
- Production Specialist 1 **School of Medicine, Stanford, California, United States** **New** Research Post Date 4 days ago Requisition # 105177 Stanford University is ... materials biomanufacturing consistent with principles of current Good Manufacturing Practice ( cGMP ) and aligned with the clinical trial investigational phase for… more
- Fujifilm (College Station, TX)
- …and embedding of the Data Integrity projects at FDBT. The Quality Assurance (QA) Specialist II for Data Integrity will be responsible for the day to day running ... + Work with Quality management to implement quality systems that will enable cGMP manufacturing of pre-clinical to commercial products. + Work as a change agent… more
- Fujifilm (College Station, TX)
- …representing a source of pride for the area. The Quality Assurance (QA) Specialist II, QA Validation, under general direction, will be responsible for review and/or ... degree in a related science concentration with 1+ year of experience of cGMP supporting pharmaceutical or biotechnology products; OR + Bachelor's degree in a related… more
- Catalent Pharma Solutions (Harmans, MD)
- ** Specialist , QA - Batch Disposition** **Position Summary** Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry ... mission: to help people live better, healthier lives. Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI… more
- Cardinal Health (Van Nuys, CA)
- …improved disease diagnosis, staging, and monitoring. **_Responsibilities_** + Handles CGMP documentation review related to product release, facilities and equipment, ... the site manufactures products to meet the requirements of 21 CFR 212 ( CGMP ) + Handles and ensures quality of documentation (control, retention, and archival) to… more
- Adecco US, Inc. (North Chicago, IL)
- …cleaning procedures that must comply with current Good Manufacturing Practices ( cGMP ) and regulatory guidelines which include documentation of work procedures ... contamination cleaning methods in areas that require microbial control. * Completes cGMP documentation of training or cleaning performed on paper and electronic… more
- Catalent Pharma Solutions (Harmans, MD)
- **Sr. Specialist , QA OTF - Night Shift** **Position Summary** Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry ... healthier lives. Catalent's Harmans/BWI, MD facility is a FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies. The campus features two… more
- Astellas Pharma (Westborough, MA)
- **Facility Engineering Compliance Specialist ** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are ... in Massachusetts. Astellas is announcing a **Facility Engineering Compliance Specialist ** opportunity at their **Astellas Institute for Regenerative Medicine… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- Analytical Quality Assurance Specialist (Microbiology) Department: Analytical QA Location: Monroe, NC START YOUR APPLICATION ... research-based pharmaceutical company. POSITION SUMMARY: The Analytical Quality Assurance (AQA) Specialist will work with the Quality Control team to work side… more
- Fujifilm (Thousand Oaks, CA)
- …will fuel your passion, energy and drive - what we call Genki.** The Specialist QA, Compliance supports the Cellular Therapy GMP quality program. This individual is ... (BPO) for the Audits and Inspections process and Risk Management Process **External US** ** Specialist QA, Compliance** **The work we do at FDB has never been more… more
- ThermoFisher Scientific (St. Louis, MO)
- …gloves, lab coat, ear plugs etc.) **Job Description** **Operations Compliance Specialist ** When you join Thermo Fisher Scientific, you'll have the opportunity ... to make the world healthier, cleaner, and safer. As an Operations Compliance Specialist , you'll play a vital role in ensuring that our manufacturing operations are… more
- Regeneron Pharmaceuticals (East Greenbush, NY)
- We are currently looking to fill a Principal External Manufacturing Specialist role. The External Manufacturing Principal Specialist provides technical and ... completion of associated operations/documentation, and assist in the monitoring of cGMP compliance at drug product contract manufacturers. As a Principal External… more
- Endo International (Rochester, MI)
- …join our team. **Job Description Summary** The Associate Process Engineer, Prep Service Specialist , works in a hands-on capacity in a fast-paced, cGMP ... production support areas to process sterile and aseptic products. The specialist works in collaboration with Operations, Maintenance, Engineering, Supply Chain,… more