Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Are you ready to join a team that is leading the way in life sciences and making a tangible impact on millions of lives? At Lonza AG, we are searching for an exceptionally skilled Sr. QA Officer to be an outstanding cornerstone of our operations in Geleen, Netherlands. This role offers an outstanding opportunity to influence and ensure the highest quality standards in a world-class organization!

KEY REQUIREMENTS:

• Educational Background: Applicants should possess a B.Sc. or M.Sc. level of thinking & working, or equivalent experience.
• Relevant Experience: 3 to 5+ years of relevant working experience is required.
• Legal Requirements: Must have a valid Dutch working permit.
• Relocation Support: Lonza offers financial support to assist candidates in transitioning to the new location.
  Join us at Lonza AG, where your contributions will help us achieve ambitious goals and make a profound impact on the world. We believe in encouraging an inclusive and collaborative environment where your ideas can flourish and drive our success. Apply now and become a part of a team that values excellence and innovation!
  We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
  Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
  People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference

• Partner with internal customers on minor change requests, CAPA, and Deviations, ensuring strict adherence to quality standards.
• Review and prepare batch records for QP’s batch disposition, and manage related deviations, CAPAs, and Change Requests within defined timelines.
• Ensure batch records are closed and archived once all batch-related activities are completed flawlessly.
• Review and approve Lonza documents such as SOPs, forms, master batch records, test methods, and checklists, maintaining our world-class documentation standards.
• Participate in QA On the Floor tasks, witnessing manufacturing, production support, warehouse, and quality control activities to ensure quality integrity.
• Assist the QA department in monitoring and measuring performance indicators and quality metrics during meetings, driving continuous improvement.
• Flexibility to do shifts when needed, ensuring QA OTF tasks are performed and that batch disposition of products with short expiry dates is completed on time.
• Perform other duties as assigned, contributing to the overall success and quality assurance of our projects.