QA Associate

R&D Partners is seeking to hire a QA Associate in Norton, MA.

• Provide raw material support, including review/approval of incoming material documentation and release for GMP use.
• Deliver on-the-floor QA support to manufacturing, including area clearance and changeover operations, ensuring readiness for production activities.
• Review and approve SOPs, master batch records (MBRs), specifications, risk assessments, and quality documents.
• Generate and maintain quality-related SOPs and controlled forms.
• Review and approve validation documents and protocol executions to confirm compliance with approved procedures and regulatory requirements.

• Bachelor's degree in a scientific or engineering discipline (Biology, Chemistry, Biotechnology, etc.) or equivalent experience.
• 2-4 years of GMP experience in Quality, Manufacturing, or QC.
• Knowledge of cGMP regulations (21 CFR Parts 210/211/11, ICH Q7/Q10) and Good Documentation Practices.
• Strong attention to detail, organizational skills, and the ability to communicate effectively across teams.
• Experience with quality systems (e.g., Veeva, SAP) is a plus.

• Medical insurance - PPO, HMO
• Dental & Vision insurance
• 401k plan
• Employee Assistance Program
• Long-term disability
• Weekly payroll
• Expense reimbursement
• Online timecard approval

$83,200 - $104,000 (Dependent on Experience)

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.

As an employee, you have access to a comprehensive benefits package.

R&D Partners is an equal-opportunity employer.

If you are interested in applying to this exciting opportunity, please click 'Apply' or visit the 'Contact Us' page to speak to one of our specialists.

R&D Partners is acting as an Employment Agency in relation to this vacancy.