• Quality Assurance, Compliance Specialist

    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 (12/18/24)
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  • Quality Control Analyst II,…

    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
    Astellas Pharma (01/09/25)
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  • Validation Specialist, Quality Assurance

    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 5+ years of industry experience in biotechnological and/or pharmaceutical quality , manufacturing , or other industry requiring high technical aptitude… more
    Astellas Pharma (01/16/25)
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  • Manager, Analytical Development (Onsite)

    ThermoFisher Scientific (Plainville, MA)
    …support a streamlined approach to Process Development. You will be supporting assay transfer to Quality Control ( QC ) for cGMP testing. This is a hands-on ... with process development groups to effectively support process development/characterization testing and QC team for assay transfer for GMP testing + Lead… more
    ThermoFisher Scientific (01/25/25)
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  • LIMS Principle System Administrator

    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
    Astellas Pharma (01/08/25)
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