QA Specialist

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

Benefits offered by this job

Growth opportunities

Inclusive, collaborative workplace

Competitive compensation

Comprehensive location-based benefits

Job summary

Lonza Geleen in the Netherlands is seeking a QA Specialist / Officer II to ensure GMP-compliant manufacturing and robust quality processes. You will partner with manufacturing and cross-functional teams, review batch records, and approve quality events, deviations, CAPAs and change controls.

This fully site-based role supports real-time collaboration and continuous improvement across production, quality control, and warehouse operations. A relevant degree and strong English are required.

Qualifications

• Bachelor's or Master's degree in Biotechnology, Life Sciences, Chemistry or related field.
• Experience in GMP-regulated manufacturing environments, ideally biotechnology/pharma.
• Proven QA knowledge and experience with GMP regulations and compliance.

Responsibilities

• Review batch records and prepare documentation for batch disposition.
• Review and approve quality events including deviations, investigations, CAPAs and change controls.
• Review and approve quality documentation (SOPs, master batch records, protocols, reports).
• Provide quality oversight on the floor during manufacturing, warehousing and QC operations.
• Support quality metrics, KPI reporting and cross-functional quality meetings.

Skills

GMP knowledge

Quality Assurance experience

Attention to detail

Communication & collaboration

English proficiency

Cross-functional teamwork

Education

Bachelor's or Master's in Biotechnology/Life Sciences/Chemistry

Job description

Geleen, Netherlands

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 and approve quality documentation including SOPs, master batch records, protocols, reports, forms and related documentation within the document management system.
• Support QA on the Floor activities by providing quality oversight during manufacturing, warehouse and quality control operations.
• Contribute to quality metrics, KPI reporting and cross‑functional quality meetings to support continuous improvement initiatives.
• Ensure batch documentation is completed, archived and product labels are issued or verified in accordance with established procedures.

What we are looking for

• Bachelor's or Master's degree in Biotechnology, Life Sciences, Chemistry or another relevant scientific discipline.
• Experience working in a GMP-regulated manufacturing environment, ideally within biotechnology or pharmaceutical manufacturing.
• Experience in Quality Assurance or a related quality function with knowledge of GMP regulations and compliance requirements.
• Strong attention to detail with the ability to review technical documentation accurately and identify compliance risks.
• Excellent communication and collaboration skills, with the ability to build effective relationships across cross‑functional teams.
• Ability to prioritize multiple activities, solve problems effectively and elevate issues appropriately when required.
• Business‑fluent English, both written and spoken.

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Reference: R78593