Wasserburger Arzneimittelwerk GmbH | Germany | 08xxx Zwickau | Permanent position | Full time | Published since: 30.01.2026 on stepstone.de
QA Manager (m/f/d)
Recipharm is a leading CDMO company in the pharmaceutical industry. Our services include the production of pharmaceuticals in various dosage forms, the production of clinical trial materials including API, and pharmaceutical product development. Recipharm employs over 6,000 people worldwide, including over 450 in the daughter of Aesica Pharmaceuticals GmbH in Monheim and Zwickau. For the succession of retirement we are looking for a pension from 01.04.2026 in 08056 Zwickau Manager (m/w/d) In this function, you act as a QA key contact person to defined customers with regard to compliance with regulatory requirements for the production and testing of pharmaceuticals at the site. They support our customers in implementing regulatory requirements and are responsible for pharmaceutical & quality aspects and issues. In addition, you support the compliance and further development of our quality assurance systems. .
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Your tasks • Your profile • What we offer
Responsible care of selected customers and their products at the site Creation and modification of specifications for active substances and medicinal products Examination of prescriptions for medicinal products and process validation documents Creation, Evaluation & Coordination of Pharmaceutical Product Changes (Change Control) taking into account current guidelines and customer requirements Processing of offers/requests, e.g. in the context of new products or changes QA Monitoring of development activities in the context of the introduction/transfer of medicinal products Creation and coordination of quality assurance agreements with customers and active substance suppliers Creation of Product Quality Reviews Processing Global Regulatory Affairs requirements for Zwickau Participation in audits and inspections (including self-inspections)
Successfully completed study of pharmacy, natural sciences or a comparable qualification At least 2 years of experience in the pharmaceutical environment (quality assurance) GMP identifiers for the production, quality and approval of medicinal products Good knowledge of GMP regulations and current legislation (AMG, AMWHV) Above-average engagement, enforcement, team spirit, communication strength and service-oriented action Very good English skills in word and writing Safe handling of MS Office
Valuable collegial cooperation & design spaces for implementing ideas Competitive & performance-oriented remuneration by domestic collective agreement permanent full-time job with 38.5 hours weekly working time; 31.5 days of annual leave Holiday allowance, annual special payment and health-promoting employee offers Other services such as employee-funded pensions & occupational health insurance
Location
 | Wasserburger Arzneimittelwerk GmbH | |
| 08056 Zwickau | ||
| Germany |
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