What are the responsibilities and job description for the Quality Assurance Specialist position at R&D Partners?
Responsibilities:
- Document Management
- Redline and initiate Finished Goods Specification creation and revisions
- Upload any new External Manufacturing documents in doc control system, e.g., Master Production Records, Specifications, BOMs
- Route SOPs for review/approval
- Initiate External Deviations & Change Control
- Create records within eQMS to document external deviations and change controls
Requirements:
- Bachelor’s degree in a scientific discipline (e.g., Biology, Chemistry, Engineering) or equivalent combination of education and experience.
- Minimum 1–3 years of experience in a quality assurance/quality operations role within a regulated manufacturing environment, preferably in finished goods.
- Working knowledge of GMP, ISO standards, and regulatory requirements for finished goods manufacturing
- Proficiency with Microsoft Office Suite (Excel, Word, PowerPoint) and familiarity with quality management systems (QMS).
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.
Salary : $90,000 - $95,000
