Vetter Pharma-Fertigung GmbH & Co. KG | Germany | 88xxx Ravensburg | Permanent position | Part time - flexible | Published since: 27.08.2025 on stepstone.de
Quality Manager Material Compliance Part-time 50% (m/w/d)
Vetter is one of the world's leading pharmaceutical service providers for germ-free filling and packaging of syringes and other injection systems - including for treating diseases such as multiple sclerosis, severe rheumatic arthritis and cancer. The globally operating company supports drug manufacturers from the early development of new products to the global market supply.
Quality Manager Material Compliance Part-time 50% (m/w/d)
Place of work: Ravensburg JOBV1_EN
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Your tasks • Your profile • What we offer
Vetter is one of the world's leading pharmaceutical service providers for germ-free filling and packaging of syringes and other injection systems - including for treating diseases such as multiple sclerosis, severe rheumatic arthritis and cancer. The globally operating company supports drug manufacturers from the early development of new products to the global market supply.
Quality Manager Material Compliance Part-time 50% (m/w/d)
Place of work: Ravensburg
People around the world rely on cousins. We rely on you: You deal with the material compliance of pharmaceutical starting materials (active and auxiliary substances) and product-contacting materials (e.g. process materials, primary packaging materials) You are a specialist in our company for the various material compliance topics, e.g. TSE compliance, virus safety, mycoplasma freedom, nitrosamines, metal impurities, extractables, allergens, melamine, GMO, phthalates, bisphenol A etc. and answer internal, customer and authorities requests You evaluate the information of our international customers regarding TSE compliance, virus safety, mycoplasma freedom and determine the necessary measures for risk analysis You evaluate the Vetter manufacturing processes with regard to nitrosamine, metal impurities, and extractables and maintain the associated risk systems You deal with the regulations and implement new or amended requirements in the company You analyze problems and questions, develop new concepts and optimize established processes You conduct internal training and present the above-mentioned topics in customer audits You check changes of our customers and suppliers in the change control process, if necessary Measures and assess the impact on existing risk analyses You check the statements of international suppliers and evaluate the information for compliance with internal and legal requirements You create material compliance for the medicines produced by Vetter for presentation to pharmaceutical authorities
You complete our team: With your completed scientific studies With their professional experience in the regulated environment, preferably GMP environment With your very good knowledge of German and English Their high quality awareness and affinity on regulatory issues Your conscientious, structured and independent way of working Through their team spirit and their very good communication skills With your good knowledge of German (min. C1-Level) so that you can document your work optimally and communicate with everyone in the team Parttime 50 %
• Responsive tasks in a family-run company in the region • Working environment in modern production and workplaces • Intensive integration into your new tasks by direct colleagues • Attractive remuneration • Operational health management (BGM) and various fitness and sports offers • Vetter Kids Holiday care • Vetter Holiday homes JOBV1_EN
Company location
Location
![]() | Vetter Pharma-Fertigung GmbH & Co. KG | |
Ravensburg | ||
Germany |
The text of this ad was translated from German into English using an automatic translation system and may contain semantic and lexical errors. Therefore, it should be used for introductory purposes only. For more detailed information, see the original text of the ad at the link below.
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