QC Technical Expert, Geleen

QC Technical Expert Location:

Geleen

Contract:

12 Month Fixed Term Contract

We are looking for a QC Technical Expert to join our company. You will be required to apply scientific skills, knowledge and experience to provide advice and propose improvements where required. The position needs to thoroughly understand the activities linked to the applicable expertise, risk analysis, method implementation and other QC related issues in the branch.

What You Will Get

A varied laboratory role with the opportunity to grow skills across several QC disciplines.

Hands-on experience with a wide range of assays, techniques and GMP processes.

A supportive team environment with training, coaching and clear development pathways.

The chance to contribute directly to the quality and safety of life-changing therapies.

What You Will Do

Act as a representative of the QC department for Quality Control topics, with close collaboration with manufacturing during team meetings, Quality Councils, client meetings if applicable.

Apply scientific skills, knowledge and experience to provide advice and propose improvements where required.

Participate in the gap assessment, transfer, validation and implementation of new QC methods and equipment.

Write, review, and approve quality documents (SOPs, stability protocols, reports, and quality instructions).

Draft and review method validation protocols and reports in line with regulatory guidelines and participate in execution of method validation activities.

Generate, review and approve QC documents and act as expert for QC during internal and external audits and inspections.

What We Are Looking For

Hands-on experience (5+ years) in QC laboratory or related role within the pharmaceutical, biotechnology or similar industry.

Extensive practical and technical knowledge of LC-MS and HPLC based methods and other laboratory techniques (e.g., ELISA, UV Spec).

Subject Matter Expert in QC assays; LC-MS, HPLC.

Effective trainer and imparts regular trainings to QC team members.

Extensive experience in Analytical Method Validation.

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.

Ready to shape the future of life sciences? Apply now.

Reference: R76138

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