Qualified Person (m/f/d)

With over 15 years of experience in the classic pharmaceutical industry, biotechnology, chemistry and medical technology, we know the key contact persons who write out demanding tasks with potential. The high demand for personnel opens up exciting opportunities for dedicated professionals and managers to develop professionally and work on their own careers. As a specialized staff consultancy with an international network, we offer you decisive advantages - and this is completely free of charge for you. Register and benefit from interesting and matching positions and projects. About the company

For an internationally active pharmaceutical company, we are looking for an experienced Qualified Person (QP) according to Paragraf 14 AMG as part of an exclusive occupation. The company has modern production sites, an international network and many years of history in the production of high-quality medicines. In this responsible position, you take over not only batch certification and release, but also actively support the Quality team in quality-relevant issues and make an important contribution to ensuring the highest GMP standards. As a modern company, our client is constantly evolving and is constantly evolving.

Responsibility for batch certification and batch release according to Graph 14 AMG Ensuring compliance with GMP requirements and regulatory requirements Assessment of deviations, change controls and CAPA measures Support of the Quality Assurance Team for quality issues Monitoring and ensuring compliance along the supply chain Cooperation with external manufacturers, suppliers and service providers Audit and inspection support Close cooperation with internal and external quality experts Active participation in the continuous improvement of quality processes

Recognition as a qualified person (Qualified Person) according to paragraph 14 AMG Completed scientific studies, preferably pharmacy, chemistry or comparable Professional experience in the pharmaceutical industry Experience in production plants of pharmaceutical production knowledge of the production of solid dosage forms, ideally tablet and capsule production Practical experience in QA and/or QC functions Very good knowledge of GMP requirements and regulatory requirements Hands-on mentality and strong team orientation Very good knowledge of German and English

Long-term position with high visibility within the quality range Possibility to take over perspectively extended responsibility Working in an experienced and collegial quality team International environment with short decision-making Hybrid working model with about 2-3 days per week Attractive compensation package including bonus Content information

Attractive social benefits Attractive, performance-oriented remuneration