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Deputy Head of Quality Control (m/f/d) – Pharmaceuticals

Dresden
Full-time
Temporary

Your chance with us

Would you like to join an internationally active company in a future-proof industry?
Due to our ongoing growth, we’re offering a position—initially for a two-year fixed term—in a modern work environment surrounded by nature (01328 Dresden). As Deputy Head of Quality Control (m/f/d), you can expect exciting responsibilities, flexible work schedules, and attractive benefits for an optimal work-life balance.

More than just a job

  • A position initially limited to two years at a future-proof, internationally active company
  • Flexible work schedules to help you best balance family and career
  • 30 vacation days to recharge
  • 10 paid days off when your child is sick to support your family
  • A modern workplace (e.g., height-adjustable desks) surrounded by greenery
  • Company parking and electric vehicle charging stations
  • 3 days off at the company’s discretion
  • Access to a diverse selection of attractive benefits through our ROTOP Benefits Portal
  • Job-Rad and Jobticket for sustainable mobility
  • Team-building company events to foster a strong sense of community
  • Diverse career and development opportunities and additional benefits

Your tasks

  • Review and evaluation of test reports for active pharmaceutical ingredients, starting materials, and drug products
  • Ensuring analytical compliance with pharmacopeia monographs as well as EU and FDA GMP requirements
  • Review and evaluation of GMP-related documents
  • Handling of OOS results and deviations, including root cause analyses and risk assessments
  • Evaluation of stability studies and trend analyses, as well as approval of validations and verifications of analytical test methods
  • Participation in supplier audits and audits of contract manufacturers

Your profile

  • Professional experience in pharmaceutical quality control and in-depth knowledge of analytical methods
  • Good knowledge of current EU and FDA GMP requirements
  • Experience in evaluating analytical results and GMP-related documentation
  • Knowledge of handling out-of-specification (OOS) results, deviations, root cause analyses, and risk assessments
  • Initial technical or disciplinary leadership experience is a plus
  • Very good written and spoken German and good written and spoken English

Your team

Join our dedicated team and play an active role in shaping the future of our company.

If you’d like to contribute your skills in an innovative environment and further your personal development, we look forward to receiving your application.
Apply now directly through our online application portal: https://rotop-pharmaka-gmbh.jobs.personio.de/

About us

We are ROTOP Pharmaka GmbH, a leading pharmaceutical manufacturer in Germany, headquartered in Dresden-Rossendorf. For more than 25 years, we have developed, manufactured, and supplied cGMP-compliant radiopharmaceuticals for diagnostics and therapy in nuclear medicine and molecular imaging – distributed to more than 40 countries worldwide.

The ROTOP brand stands for quality, reliability, and pharmaceutical expertise. As a radiopharmaceutical manufacturer, we focus on close customer relationships, collaborative partnerships, and tailored radiopharmaceutical solutions for hospitals, clinics, and research partners. Our mission: advancing the medicine of tomorrow – developed and manufactured with responsibility.

ROTOP Pharmaka stands for integrity, expertise, and commitment – from Dresden to the future of nuclear medicine.