QC Software and Application specialist

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.

Seeking an exceptionally dedicated QC and Software Specialist to join our ambitious team in Geleen, Netherlands, and make a significant impact in life sciences.

Key responsibilities:

• Manage LIMS projects, including master data creation, modification, and updates.
• Validate and maintain spreadsheets used for data analysis and reporting.
• Assist in technical writing tasks such as SOPs, protocols, and reports.
• Perform routine software and system administration.
• Collaborate with cross-functional teams to ensure compliance with regulatory standards and internal quality procedures.
• Conduct commercial trending analysis to identify patterns, deviations, and opportunities for improvement.
• Participate in continuous improvement initiatives to improve efficiency and effectiveness within the QC department.
• Provide support and mentorship to junior team members as vital.
• Coordinate compliance responsibilities within QC areas, ensuring adherence to regulatory requirements and internal quality standards.
• Lead and contribute to significant improvements affecting the entire QC organization, driving initiatives for enhanced processes, technologies, and methodologies.
• Work on deviations and CAPAs affecting the QC organization, conducting detailed investigations and implementing effective corrective actions.
• Coordinate and lead all aspects of shipments of samples and materials as needed.
• Perform additional activities related to housekeeping, material management, equipment readiness, general trainings, and internal shipments to ensure smooth operations within the QC department.

Key requirements:

• Bachelor’s degree in a relevant scientific field (e.g., chemistry, biology, or related subject area).
• Minimum of 2 years of experience in a QC or related role within the pharmaceutical, biotechnology, or similar industry.
• Proficiency in LIMS software and experience with master data creation and modification.
• Strong analytical skills with the ability to collaborate effectively with cross-functional teams.
• Diligent with a dedication to maintaining high-quality standards.
• Experience in technical writing and documentation is preferred.

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.