ECA Recruiters
Product Quality Lead – Pharmaceutical Opportunity
Role Highlights:
Lead QA review of manufacturing and packaging records and ensure GMP‑compliant product release
Drive deviations, CAPA, investigations, batch disposition, audits, and quality escalations
Partner with CMOs on quality performance, material/component changes, and QTA compliance
Support lifecycle activities: stability, APRs, mock recalls, complaints, and continuous improvement
Contribute to SOP/WI updates, change control, and quality‑impacting initiatives
Requirements: BS in science, 5+ yrs QA experience, strong GMP + sterile/aseptic background
Compensation: $100–$130K base + 10% AIP, full benefits
Travel to manufacturing facilities throughout the year. Hybrid: Onsite in Richmond Tues–Thurs. Relocation package offered for candidates outside Richmond area.
Responsibilities
Review and sign off manufacturing and packaging records to release product
Manage deviations, CAPAs, batch investigations, audits, and quality escalations
Collaborate with CMOs on quality performance and compliance matters
Assist with stability studies, APRs, mock recalls, and complaint investigations
Implement SOP, WI updates and change control processes
Requirements
Bachelor’s degree in a scientific discipline
5+ years working in quality within pharma, medical device or FDA‑regulated manufacturing
Experience with sterile/aseptic manufacturing
Seniority Level Mid‑Senior level
Employment Type Full‑time
Job Function Quality Assurance, Product Management, and Manufacturing
Industries Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing
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Lead QA review of manufacturing and packaging records and ensure GMP‑compliant product release
Drive deviations, CAPA, investigations, batch disposition, audits, and quality escalations
Partner with CMOs on quality performance, material/component changes, and QTA compliance
Support lifecycle activities: stability, APRs, mock recalls, complaints, and continuous improvement
Contribute to SOP/WI updates, change control, and quality‑impacting initiatives
Requirements: BS in science, 5+ yrs QA experience, strong GMP + sterile/aseptic background
Compensation: $100–$130K base + 10% AIP, full benefits
Travel to manufacturing facilities throughout the year. Hybrid: Onsite in Richmond Tues–Thurs. Relocation package offered for candidates outside Richmond area.
Responsibilities
Review and sign off manufacturing and packaging records to release product
Manage deviations, CAPAs, batch investigations, audits, and quality escalations
Collaborate with CMOs on quality performance and compliance matters
Assist with stability studies, APRs, mock recalls, and complaint investigations
Implement SOP, WI updates and change control processes
Requirements
Bachelor’s degree in a scientific discipline
5+ years working in quality within pharma, medical device or FDA‑regulated manufacturing
Experience with sterile/aseptic manufacturing
Seniority Level Mid‑Senior level
Employment Type Full‑time
Job Function Quality Assurance, Product Management, and Manufacturing
Industries Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing
#J-18808-Ljbffr