Quality Assurance Engineer – Pharmaceutical Manufacturing

We are partnered with a major pharmaceutical manufacturing company that is seeking a Quality Assurance Engineer to support quality systems, investigations, and GMP compliance within a regulated production environment.

This role is well suited for someone with hands-on QA experience who enjoys problem-solving, cross-functional work, and supporting continuous improvement initiatives.

Schedule: Monday–Friday, standard business hours

Key Responsibilities

• Support and lead deviation and nonconformance investigations, including CAPA activities
• Review and manage change controls related to manufacturing and quality documentation
• Apply root cause analysis and risk assessment tools to support investigations and quality initiatives
• Analyze quality and operational data to identify trends and improvement opportunities
• Support product quality reviews and ongoing quality system maintenance
• Assist with regulatory and customer audits as needed
• Ensure day-to-day GMP compliance across manufacturing operations

Qualifications

• Bachelor’s degree in a scientific or technical discipline preferred (or equivalent experience)
• 3+ years of quality assurance experience in pharmaceutical, biotech, or regulated manufacturing
• Working knowledge of GMPs and quality systems
• Strong analytical, organizational, and documentation skills
• Comfortable working independently and in a team environment
• Proficient with Microsoft Office and electronic documentation systems