Scientist for Analytical Testing and Verification | Scientist Analytische Testungen und Verifikation (m/w/d)
Randstad Professional
Job Summary
This role is based in Ludwigshafen within the Devices and Combination Product Development department of a leading pharmaceutical R&D environment. You will be responsible for the analytical characterization of combination products, such as parenteral application systems and autoinjectors. Day-to-day activities include planning, executing, and documenting design verification tests, with a specific focus on visual and functional force measurements using material testing equipment. You will develop and validate test methods, transfer methods to other departments, and ensure all activities comply with strict GMP quality standards. The position requires close collaboration with global teams, particularly in the USA, and involves participation in international meetings. This is an attractive opportunity for a technical professional to work on cutting-edge biological products within a dynamic, innovative team that offers long-term job security, comprehensive social benefits, and a structured corporate environment.
Required Skills
Education
Degree in Engineering (Physics, Pharmaceutical Technology, Packaging Technology, Biotechnology, Process Engineering, Plastics Technology, Materials Science, or Materials Testing) or completed vocational training as BTA, MTA, CTA, or Biology/Chemistry Laboratory Assistant with relevant experience.
Experience
- Professional experience in physical and functional testing, specifically force measurements on material testing machines
- Several years of professional experience if coming from a vocational training background (BTA/MTA/CTA/Laboratory Technician)
- Experience working within a regulated GMP environment
- Experience in independent planning, execution, and evaluation of experiments
- Experience in creating technical reports and presentations in English
Languages
Additional
- The role requires the ability to work in Ludwigshafen and collaborate with international sites (USA). Must be proficient in using electronic documentation systems for GMP-compliant reporting.
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