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Quality Control Documentation Assistant – Pharmaceuticals (m/f/d)

Dresden
Full or part-time
Permanent employee

Your chance with us

Would you like to join an internationally active company in a future-proof industry?
Due to our ongoing growth, we are offering a permanent position in a modern work environment surrounded by nature (01328 Dresden). As a Quality Control Documentation Assistant – Pharmaceuticals (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 permanent position 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 to care for a sick child, 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 your discretion / “K.O.” days
  • 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 togetherness
  • Diverse career and development opportunities and additional benefits

Your tasks

  • Creation, maintenance, and revision of GMP-compliant documents in the area of quality control
  • Management and archiving of lab reports, quality data, and quality-related documentation
  • Support for deviation, CAPA, and change control processes
  • Participation in laboratory work, including proper GMP documentation
  • Preparation for and support during audits and inspections
  • Ensuring complete, traceable, and quality-compliant documentation

Your profile

  • Completed vocational training in the natural sciences, pharmaceuticals, or a comparable field
  • Ideally, professional experience in the pharmaceutical industry, quality control, in a laboratory, or in a regulated environment
  • Basic knowledge of GMP requirements and pharmaceutical documentation practices is a plus
  • Very good written and spoken German
  • Proficiency with MS Office and willingness to learn subject-specific systems
  • Meticulous, structured, and reliable work style, as well as a strong commitment to quality and teamwork

Your team

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

If you’d like to apply 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.