Quality Assurance Operations Specialist
5 days ago
R&D Partners is seeking a highly skilled Quality Assurance Operations Associate to provide quality oversight for GMP documentation. This is a 4-month contract with the potential to extend.
Key Responsibilities- Provide quality oversight of one or more portions of operations, including:
- Review of GMP documentation from manufacturing, which includes logbooks, production batch records, and electronic buffer & media batch records.
- Scanning and archiving executed production batch records.
- Ensure manufacturing adherence to company policies, procedures, regulatory licenses, industry standards, and GMP regulations.
- Working knowledge of United States and European regulatory requirements, guidelines, and recommendations is a plus (additional jurisdictions a plus).
- Perform other duties and projects as assigned by management.
- Associate's degree or higher.
- 2+ years of Biotechnology or Biopharmaceutical quality assurance experience.
- Comprehensive benefits package, including medical insurance, dental & vision insurance, 401k plan, employee assistance program, long-term disability, weekly payroll, expense reimbursement, and online timecard approval.
R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
R&D Partners is an equal-opportunity employer.
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