Experienced QC Chemist
21h21 hours agoPolyPeptide Group
Malmö, SE · Full-time · SEK 500,000 – SEK 650,000
About this role
Seeking an Experienced QC Chemist to apply analytical and innovative skills in quality control of starting materials or API. Join a large Quality Control department striving to improve processes and secure the supply chain. Contribute to a meaningful job impacting people's lives and health.
Ensure analyses meet regulatory GMP requirements for release of starting materials and/or API using techniques like HPLC, GC/IC, LC-MS, and pharmacopeia analyses. Handle post-controls, stability studies, method validations, specifications, and more. The role involves independent execution and responsibility for key analytical tasks.
The department consists of about 50 people divided into three teams focusing on contract manufacturing & customer projects, raw materials/starting materials, and systems. Collaboration is essential as teams share facilities and equipment. Work in a collaborative environment despite different team focuses.
Drive continuous improvement within QC and act as a knowledge resource on analytical methods and GMP. Thrive in a fast-paced, changing environment at PolyPeptide, a CDMO for peptide and oligonucleotide active pharmaceutical ingredients. Support pharma and biotech customers contributing to global patient health.
Requirements
- University degree in analytical chemistry or equivalent
- Several years of laboratory work experience in the pharmaceutical industry (GMP)
- Very good experience of analytical techniques such as HPLC, GC, IC, LC-MS
- Experience of mentoring and training colleagues
- Very good knowledge of Swedish and English, both spoken and written
- Positive attitude with ease in collaboration and independent work
- Responsible, solution-oriented with ability to take initiatives
Responsibilities
- Independently perform and take responsibility for release analyses of API and intermediates
- Evaluate, report, and review analysis results
- Drive and participate in laboratory investigations and deviation management
- Participate as needed in validation and method transfer/implementation of analytical methods
- Contribute to and drive continuous improvement work within QC
- Act as knowledge resource within analytical methods and GMP
Benefits
- Part of a large QC department improving processes and securing supply chain
- Meaningful role contributing to people's lives and health
- Attractive work environment where employees and business develop together
- Opportunity to challenge yourself and influence improvements
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