Our client is a leading pharmaceutical company with a state-of-the-art production site in the Neuchâtel area, operating globally and ranking among the largest employers in the industry in Switzerland. To strengthen the team, we are looking for an experienced professional as
QC Specialist, New Raw Material Introduction (Ref. 2584) - 6-month temporary contract
In this role, you will play a key part in the integration of new raw materials into the QC Laboratory and lead method validation and specification setting. You will work cross-functionally with departments such as QC, Analytical Development, Regulatory Affairs, and Supply Chain, while reporting to the Senior Manager QC NPI.
Your main tasks
- Represent QC in cross-functional teams for New Product Introduction and raw material qualification
- Lead and support analytical method transfers, verifications, and validations
- Develop and write analytical methods, protocols, reports, and specifications
- Define and document incoming testing specifications for new raw materials
- Coordinate and evaluate testing of trial materials in collaboration with internal teams and external labs
- Support installation and qualification of new laboratory equipment and ensure proper training for QC staff
- Review compendial changes and manage related change controls in compliance with GMP standards
- Assist with resource planning and scheduling of incoming material testing activities
- Act as technical point of contact for raw material topics in the absence of the Senior Manager
- Promote continuous improvement initiatives within QC operations related to incoming material processes
Your profile
- Degree in Science, Chemistry, or similar field (CFC as Laboratory Technician or BSc level)
- At least 5 years of experience in a GMP-regulated environment
- Strong expertise in analytical method development, transfer, and validation
- Sound knowledge of regulatory compendia (Ph. Eur., USP, JP) and GMP requirements
- Practical experience with chromatography (HPLC, UPLC, GC) and classical wet chemistry techniques
- Proficient in scientific writing and GMP documentation (protocols, reports, procedures)
- Ability to troubleshoot analytical issues and support junior analysts when needed
- Detail-oriented, self-motivated, and able to manage multiple priorities independently
- Fluent in French and English, with strong communication and organizational skill
Domagoj Odrljin is looking forward to receiving your application documents via our job portal (CV, diploma, reference letters; no motivational letter necessary).
Full discretion is guaranteed and we will gladly answer any additional questions.