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.
Participates in the gap assessment, transfer, validation and implementation of new QC methods and equipment.
Write, review, and approval of quality documents (SOPs, stability protocols, reports, and quality instructions).
Draft and review method validation protocols and reports in line with regulatory guidelines. Participate in execution of method validation activities.
Generate, review and approve QC documents and acts as expert for QC during internal and external audits and inspections.
Requirements
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.
About Lonza
Ready to shape the future of life sciences?
Additional Information
Job Title: QC Technical Expert
Location: Geleen
12 Month Fixed Term Contract
We are looking for a QC Technical Expert to join our company and 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 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.
The full-time annual base pay for this position in The Netherlands is expected to range between EUR 54'000 and EUR 75'600 . Initial salary placement within this range will be determined based on role-related factors such as experience, qualifications, and expected contribution.