Qualification and Validation Specialist | Mitarbeiter (m/w/d) Qualifizierung / Validierung
Eckert & Ziegler Radiopharma GmbH Braunschweig
Job Summary
As a Qualification and Validation Specialist at Eckert & Ziegler Radiopharma GmbH, you will play a vital role in the production of radiopharmaceuticals used in cancer diagnosis and therapy. Your daily responsibilities involve creating qualification and validation documentation for manufacturing processes and analytical methods, as well as performing the actual validations. You will contribute scientifically to projects involving the construction of production facilities for pharmaceuticals and medical devices. Additionally, you will maintain the GMP status of all site equipment through maintenance and calibration planning, while utilizing complex laboratory equipment like HPLC and ICP-MS. This role is ideal for professionals with a background in natural sciences or engineering who want to work in a highly regulated life-sciences environment. The position offers a stable, long-term perspective with a focus on work-life balance, featuring flexible working hours, no shift work, and 30 days of annual leave.
Required Skills
Education
Completed degree in Natural Sciences or Engineering (e.g., Chemistry, Biotechnology, or Process Engineering).
Experience
- Professional experience in a GMP-regulated environment, preferably within the pharmaceutical or life-sciences industry
- Practical experience operating analytical laboratory equipment such as HPLC and ICP-MS
- Experience in creating qualification and validation documentation for manufacturing and analysis
- Experience handling radioactive isotopes is desirable but not mandatory
Languages
Additional
- The role requires the ability to work on-site in a laboratory environment; candidates must be comfortable working with radioactive isotopes.