GMP QA Specialist: Elevate Quality in Biotech Manufacturing

Lonza; Geleen; On-site; Confidential; Full time

Benefits offered by this job

Growth opportunities

Competitive compensation

Comprehensive benefits

Job summary

Lonza Geleen is seeking a QA Specialist / Officer II to join the site-based Quality Assurance team and support GMP operations. You will review quality documentation, guide cross-functional teams, and help drive continuous improvement across production processes.

We offer growth opportunities, a collaborative environment, and competitive compensation. The Netherlands-based full-time role emphasizes in-person collaboration to ensure the highest quality and safety standards in medicines

Qualifications

• Experience with GMP operations and quality systems is preferred.
• Ability to review documentation and ensure compliance with quality standards.
• Collaborate with manufacturing and other teams to support quality initiatives.

Responsibilities

• Act as QA SME for GMP and quality-related activities with manufacturing teams.
• Review batch records and prepare documentation for batch disposition within timelines.
• Review and approve quality events including deviations, investigations, CAPAs and change controls.

Skills

GMP knowledge

Quality assurance

Documentation review

Cross-functional collaboration

Job description

Lonza Geleen is seeking a QA Specialist / Officer II to join the site-based Quality Assurance team and support GMP operations. You will review quality documentation, guide cross-functional teams, and help drive continuous improvement across production processes.

We offer growth opportunities, a collaborative environment, and competitive compensation. The Netherlands-based full-time role emphasizes in-person collaboration to ensure the highest quality and safety standards in medicines