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PolyPeptide Group

QC Chemist

21h

PolyPeptide 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