We are looking for an experienced QC Analyst to join Europe’s largest CDMO. As a valued member of this innovative team, you will play a key role in delivering life-saving treatments to patients globally. Leverage your expertise in analytical techniques to support groundbreaking pharmaceutical products in a GMP-regulated environment.
Responsibilities:
- Perform and release in-process controls (HPLC, CE, icIEF, etc.) in compliance with cGMP guidelines.
- Support method validation activities.
- Maintain and optimize existing laboratory infrastructure.
- Conduct routine final analyses and stability sample testing, particularly for time-critical samples.
- Test and assess random product samples to ensure compliance with predefined standards.
- Aggregate and document test data accurately and efficiently.
Qualifications:
- Completed technical or scientific training, with experience in analytical work within the pharmaceutical industry preferred.
- Proficiency in HPLC techniques and hands-on laboratory experience in a GMP environment.
- Strong sense of responsibility, team-oriented mindset, and excellent communication skills.
- High-quality awareness and an efficient, reliable approach to work.
- Ability to work independently and handle potentially hazardous substances safely.
- Proficiency in using a PC and standard software applications.
Practicalities:
- Location: Visp, Switzerland.
- Duration: 6 months
- Working Model: Fully on-site position.
- Language Requirements: Fluency in English is mandatory
Ready to be part of an innovative team and make an impact in the pharmaceutical and biotech industries? Apply now or send your CV to f.karampina@panda-int.com. Don’t wait—interviews may start as early as next week!