- ThermoFisher Scientific (Worcester, MA)
- …full-time benefits. **Key responsibilities:** The QC Data Reviewer supports the data review team within a fast paced GMP environment in support of one or ... Schedule** Second Shift (Afternoons) **Environmental Conditions** Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards **Job Description** At… more
- Astellas Pharma (Westborough, MA)
- …Quality Assurance areas and will work closely with talented counterparts in the Manufacturing , Quality Control , and Materials Management teams to help ... following: + Performs QA review of executed Manufacturing batch records, QC test records, raw...Sciences, Engineering, or Chemistry, with 2-3 years of related Quality Assurance experience within GMP -regulated industry, or… more
- Astellas Pharma (Westborough, MA)
- …Quality Assurance areas and will work closely with talented counterparts in the Manufacturing , Quality Control , and Materials Management teams to help ... will perform critical QA compliance tasks in support of GMP manufacturing programs as AIRM moves through...following:** + Performs QA review of executed Manufacturing batch records, QC test records, raw… more
- Astellas Pharma (Westborough, MA)
- …for a strong GMP and scientific background and experience with quality control testing of cell-based therapies. **Essential Job Responsibilities:** + Perform ... a GMP state. + Monitor and trend QC data. + Complete routine record review ...Dimensions:** + This position interacts with Quality Control , Analytical Development, Drug Product Development, Manufacturing … more
- Astellas Pharma (Westborough, MA)
- …the AIRM GMP Environmental Monitoring (EM) program and microbial testing. QC Analyst II is responsible for perform/ review , lab testing, technical documents, ... ** Quality Control Analyst II, Microbiology** Do... QC Analyst II, Microbiology routinely interacts with Manufacturing , QC Analytical, Quality Assurance,… more
- Cambridge Isotope Laboratories, Inc. (Tewksbury, MA)
- Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Documentation Specialist, based onsite in our Tewksbury, MA facility. CIL is the ... has had consistent growth for over 40 years. The Quality Control Documentation Specialist is responsible for...of trending or support for investigative purposes. Responsibilities + Review batch data for release of GMP /ISO… more
- Astellas Pharma (Westborough, MA)
- …of Quality Assurance areas and will work closely with counterparts in the Manufacturing , Quality Control , and Materials Management teams to help ensure ... minimum of 10+ years of industry experience in biotechnological and/or pharmaceutical quality , manufacturing , or other industry requiring high technical aptitude… more
- Bristol Myers Squibb (Devens, MA)
- …with process development, manufacturing sciences and technologies, analytical development, quality control , and/or stability. + Excels at analyzing complex ... or related discipline preferred. + Minimum of 15 years of biopharmaceutical and/or quality experience in both R&D and commercial manufacturing environments. If… more
- System One (Devens, MA)
- …Regulatory expectations + Reviews and approves Quality , Quality Control , Validation and Automation related documents + Review and approves Standard ... (QA) support to Devens Site and reporting Manger through quality review and approval of Investigations and...preferred. + Advanced Level of relevant experience in a GMP , GCP, or GXP with at least 8 years… more
- Astellas Pharma (Westborough, MA)
- …team and contributes to a supportive and positive work environment. + Strong knowledge of GMP , SOPs and quality control processes. + Strong knowledge of ... site to ensure compliance to 21CFR Part 11 for manufacturing and lab equipment. **Essential Job Responsibilities:** + Develop...manage vendor IQ/OQ of equipment. + Develop, revise, and review SOPs, protocols and reports and other documents to… more