Quality assurance specialist

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

Omschrijving functie

Lonza Geleen - - 40 uur - HBO - WO QA Specialist / Officer II in Geleen The actual location of this job is in. Join our Quality Assurance team and play a key role in ensuring that life-changing medicines are manufactured to the highest quality and compliance standards. As a QA Specialist / Officer II, you will work closely with manufacturing and cross-functional teams to support GMP operations, review quality documentation, and help drive continuous improvement across our production processes. This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.

What you will get

• An agile career with opportunities for growth and development within a global life sciences company.
• An inclusive, collaborative and ethical workplace where your ideas are valued.
• Competitive compensation programs that recognize high performance.
• A comprehensive benefits package tailored to your role and location.
• Opportunities to work with cutting-edge biotechnology manufacturing technologies.
• The full list of our global benefits can be found here: https://www.lonza.com/careers/benefits

The full-time annual base pay for this position in the Netherlands is expected to range between EUR 41,250 and EUR 57,750. Initial salary placement within this range will be determined based on role-related factors such as experience, qualifications, and expected contribution.

What you will do

• Partner with manufacturing and internal stakeholders as the Quality Assurance subject matter expert, providing guidance on GMP and quality-related activities.
• Review batch records and prepare documentation for batch disposition, ensuring completion within agreed timelines.
• Review and approve quality events including deviations, investigations, CAPAs and change controls while ensuring compliance with GMP requirements.
• Review ...