Biotechnology company is hiring Quality Assurance Operations Associates to provide quality oversight for GMP documentation. This is a 4-month contract to start with the potential to extend.
Responsibilities
- Provide quality oversight of one or more portions of operations including, but not limited to:
- Review of GMP documentation from manufacturing, which can include but is not limited to 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 a plus (additional jurisdictions a plus).
- Perform other duties and projects as assigned by management.
Qualifications
- Associate's degree or higher.
- 2+ years of Biotechnology or Biopharmaceutical quality assurance experience
Pay
Why Choose R&D Partners?
As an employee, you have access to a comprehensive benefits package including:
- Medical insurance – PPO, HMO & HSA
- Dental & Vision insurance
- 401k plan
- Employee Assistance Program
- Long-term disability
- Weekly payroll
- Expense reimbursement
- 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.
