Quality Assurance Associate

Job Title:
Quality Assurance (QA) Associate

Location:
Onsite - NJ

Job Type: Contract (12+ Months)

Experience: 0–4 Years

We are seeking a motivated Quality Assurance (QA) Associate to join our pharmaceutical manufacturing team. This is an excellent opportunity for recent graduates and early-career professionals to gain hands‑on experience in a GMP-regulated environment. The QA Associate will support quality systems, documentation review, batch record review, deviation investigations, CAPA activities, and compliance with FDA regulations.

• Review batch production records for accuracy and GMP compliance.
• Support deviation investigations and CAPA documentation.
• Assist with change controls and quality events.
• Perform document control activities and SOP reviews.
• Participate in internal GMP audits.
• Ensure compliance with FDA, cGMP, ICH, and company procedures.
• Support training documentation and quality metrics.
• Collaborate with Manufacturing, QC, Validation, and Engineering teams.

• Bachelor's degree in Pharmacy, Chemistry, Biology, Biotechnology, Life Sciences, or related field.
• 0–4 years of pharmaceutical or biotech experience.
• Basic understanding of cGMP and FDA regulations.
• Strong documentation and communication skills.