Hays – Working for your tomorrow | Germany | 31xxx Hildesheim | Full time | Published since: 30.10.2026 on stepstone.de
Head of QA (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.
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Your tasks • Your profile • What we offer
Leadership and further development of the QA team including resource planning, qualification, coaching and targeted personnel development Ensuring GMP compliance, data integrity and effectiveness of the quality management system in compliance with regulatory requirements and group-wide quality standards Control and continuous optimization of quality-relevant processes, in particular deviation management, CAPA, change control, Complaints as well as management of quality risks and escalation Management and monitoring of administrative inspections, customer and supplier audits and self-inspections including Following and implementing agreed measures Responsibility for quality indicators, product quality reviews and management reports as well as derivation, implementation and follow-up of sustainable improvement measures Further development and harmonisation of quality standards, SOPs and cross-site QM processes in close cooperation with Corporate QA and other relevant stakeholders Central contact person and decision-makers for quality-critical issues as well as professional communication with authorities, customers, suppliers and internal interfaces Promoting sustainable quality culture and support for strategic quality and compliance initiatives focusing on risk management, continuous improvement and operational excellence
Completed scientific studies or comparable training, ideally pharmacy Experience in the GMP regulated environment of the pharmaceutical industry Regulatory knowledge GMP and relevant regulations, incl. Corresponding QS requirements Knowledge of quality management, audits, inspections and documentation English knowledge of Word and Writing Good understanding and technical understanding Leadership experience and strong communication and decision-makingKnowledge, reliability and care Self-employed, structured, targeted working and high commitment
Slip time International company Content information
The GVP tariff agreement applies to this position. The compensation is based on the remuneration group 9. Their specific remuneration is determined in particular taking into account qualifications and professional experience
Location
 | Hays – Working for your tomorrow | |
| Hildesheim | ||
| Germany |
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