• Pharmaceutical Quality Assurance

    ManpowerGroup (Cambridge, MA)
    …Pharmaceutical QA Specialist to join their team. As a QA Specialist , you will be part of the Quality Assurance department supporting various ... which will align successfully in the organization. **Job Title:** Pharmaceutical QA Specialist **Location:** Cambridge, MA **Pay Range:** $50-55 per… more
    ManpowerGroup (03/06/25)
    - Related Jobs
  • QA Principal Compliance Specialist

    Sanofi Group (Framingham, MA)
    …within our [Team Name], will be to [summary of opportunity]. **Department Description** Quality Assurance ( QA ) Operations is responsible for quality ... to ensure cGMPs are adhered to during manufacturing operations. Quality Assurance Operations is responsible for providing...QA review deviations * Provide off-hour support for batch record and log book issuance Represent… more
    Sanofi Group (04/29/25)
    - Related Jobs
  • Document Control Specialist

    Catalent Pharma Solutions (Chelsea, MA)
    **Document Control Specialist - Quality Assurance ** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing ... in North America. Catalent Pharma Solutions is hiring a QA Document Control Specialist who is responsible...of master documents (including but not limited to SOPs, Batch Records , Test Methods, Protocols, Reports, Specifications,… more
    Catalent Pharma Solutions (04/05/25)
    - Related Jobs
  • QA Senior Compliance Specialist

    Sanofi Group (Framingham, MA)
    …from infectious diseases and bring hope to patients and their families. Join our Quality Assurance ( QA ) Operations team at Sanofi's Framingham Biologics ... **Job title** : QA Senior Compliance Specialist , Operations **Location**...production requiring quality input. + **Compliance:** Review batch records , logbooks, equipment status documentation, cleaning… more
    Sanofi Group (04/29/25)
    - Related Jobs
  • Lead Quality Assurance Coordinator

    Integra LifeSciences (Boston, MA)
    …care. The Lead Quality Assurance Coordinator (formerly, Quality Assurance Specialist II) supports QA oversight of the Integra Boston/Braintree ... review the output of daily operational activities. Additionally, the QA Specialist II provides QA ...+ Review of production activities including completed forms and batch records against procedure requirements and product… more
    Integra LifeSciences (03/26/25)
    - Related Jobs
  • Field Quality , QA Operations Senior…

    Bristol Myers Squibb (Devens, MA)
    …manufacturing related SOPs. + May provide guidance to less experienced staff. + Support the Quality approval of Master Batch Records or Syncade Recipes. + ... and manufactured product. Assists in the identification, generation and quality review of investigation records that may...regulations and guidance. + Knowledge of electronic or paper batch record systems, DeltaV, and other electronic… more
    Bristol Myers Squibb (04/07/25)
    - Related Jobs
  • Compliance Specialist CMC

    Astellas Pharma (Westborough, MA)
    …Medicine (AIRM)** site in **Westborough, MA.** **Purpose:** The Compliance Specialist CMC, Quality Assurance will perform critical QA tasks in support of ... quality and compliance across a broad range of Quality Assurance areas and will work closely...for regulatory submissions, included but not limited to draft batch records , analytical test records ,… more
    Astellas Pharma (04/07/25)
    - Related Jobs
  • Laboratory Operations specialist

    Robert Half Office Team (Mansfield, MA)
    …including cell count, viability, and purity analysis. Conduct comprehensive reviews of Batch Records and manage Material Disposition for Fresh shipments. ... daily blood laboratory workflows, including sample receipt, handling, and storage. Ensure quality assurance and regulatory compliance (eg, CLIA, FDA, CAP) within… more
    Robert Half Office Team (04/22/25)
    - Related Jobs
  • Associate Engineering Fellow, Process Engineering

    Takeda Pharmaceuticals (Cambridge, MA)
    …teams, including process chemistry, analytical development, drug product development, manufacturing, quality assurance , and regulatory affairs, to develop and ... with methods for achieving and controlling high standards of purity and quality . The successful candidate will be recognized as a technical resource/expert within… more
    Takeda Pharmaceuticals (05/01/25)
    - Related Jobs