
QC Chemist
21h21 hours agoPolyPeptide Group
Malmö, SE · Full-time · SEK 420,000 – SEK 580,000
About this role
Seeking an exciting opportunity to apply your 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 delivering approximately 2 million doses to patients every day.
Ensure analyses meet regulatory GMP requirements for release of starting materials and/or API. Utilize techniques like HPLC, GC/IC, LC-MS, and pharmacopeia analyses. Handle stability studies, method validations, specifications, and more.
Department consists of about 50 people divided into three teams: contract manufacturing & customer projects, raw materials/starting materials, and systems. Collaboration is key as teams share facilities and equipment. Positive, collaborative environment with focus on shared goals.
PolyPeptide Group is a specialized CDMO for peptide and oligonucleotide active pharmaceutical ingredients. Operates a global network of six GMP-certified facilities in Europe, USA, and India. Core values: Trust to build relationships, Innovation to solve problems, Excellence in quality and flexibility.
Requirements
- University education with focus on analytical chemistry
- Previous work experience from the pharmaceutical industry
- Very good knowledge of Swedish and English, both spoken and written
- Professional experience with HPLC analyses
- Professional experience with LC-MS analyses
- Professional experience with AAA analyses
- Experience with Chromeleon
Responsibilities
- Perform release analyses
- Evaluate, report, and review analysis results
- Conduct or participate in laboratory investigations
- Participate in validation and method transfer/implementation of analytical methods as needed
- Participate in continuous improvement work
- Execute HPLC, GC/IC, LC-MS analyses
- Conduct pharmacopeia analyses
- Support stability studies
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