Quality Assurance Technical Writer - 171852

Zp Group Llc
  • Ridgefield, NJ
    7 days ago

    Job Description

    Responsibilities: for the Quality Assurance Technical Writer include: · Review and act as author/technical writer to alterations to Master Batch record and QA documentation · Correct and revise documentation as needed · Advise manufacturing personnel on proper documentation · Utilize knowledge of FDA and GMP regulations to ensure compliance Qualifications: for the Quality Assurance Technical Writer include: · A minimum of 1-5 years' experience within Pharmaceutical Manufacturing (sterile injectable is preferred) · Hands on experience with QA documentation · Proficiency in Microsoft Office · B.S. in business or scientific field preferred Compensation: for the Quality Assurance Technical Writer include: · Salary Range is dependent upon experience. · Comprehensive benefits package

    Numbers & Facts

    LocationRidgefield, NJ

    Skills

    • Documentationunmatched
    • Drug Manufacturingunmatched
    • FDA Requirementsunmatched
    • GMP (Good Manufacturing Practices)unmatched
    • Maintain Complianceunmatched
    • Manufacturingunmatched
    • Microsoft Officeunmatched
    • Quality Assuranceunmatched
    • Regulatory Complianceunmatched
    • Technical Writingunmatched
    • Writing Skillsunmatched

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