QA Compliance Manager – Biologics Materials & Release

Biopharma Careers; Munster; Hybrid; EUR 90,000 - 120,000; Full time

Benefits offered by this job

Annual bonus

Pension contribution

Family health insurance

27 days annual leave

On-site gym

Life assurance

Job summary

Bristol Myers Squibb is seeking a Manager, QA Compliance at the Cruiserath Biologics Manufacturing campus in Ireland. You will support material qualification, QA disposition of materials, and maintenance of QM data in SAP/MDG-M, reporting to the Senior Manager, QA Compliance Materials Management.

A strong cGMP background and 4+ years in biopharma QA are essential. The role emphasizes collaboration across cross-functional teams, participation in process improvements, and ensuring regulatory

Qualifications

• Bachelor-level science/engineering degree with strong understanding of cGMP.
• 4+ years quality experience in a biopharma environment.
• Knowledge of material qualification & SAP would be a distinct advantage.
• Strong communication and organizational skills; ability to work independently and in a team.

Responsibilities

• Support material management activities for the site, including material qualification.
• Handle supplier change notifications and risk assessments.
• Manage QA dispositions of raw materials and consumables.
• Prepare, review and approve Material Qualification Documentation and QA procedures.
• Create and maintain QM Master Data in MDG-M and SAP.
• Lead QA review for changes, deviations, investigations, CAPAs and related docs.

Skills

cGMP knowledge

Cross-functional collaboration

Education

BSc in science/engineering or related

Tools

SAP

MDG-M

Job description

Bristol Myers Squibb is seeking a Manager, QA Compliance at the Cruiserath Biologics Manufacturing campus in Ireland. You will support material qualification, QA disposition of materials, and maintenance of QM data in SAP/MDG-M, reporting to the Senior Manager, QA Compliance Materials Management.

A strong cGMP background and 4+ years in biopharma QA are essential. The role emphasizes collaboration across cross-functional teams, participation in process improvements, and ensuring regulatory