QA Specialist / Batch Record Review (m/f/d)

With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.

• Review executed electronic and/or manufacturing protocol for compliance to GMP
• Support implementation/ revision of manufacturing protocols for GMP manufacturing
• Ensure that internal/ external GMP standards and regulatory requirements are adhered to in projects
• Participate in cross-functional investigations to determine impact to product quality and the definition of associated corrective measures
• Represent the Quality Unit in cross-functional teams
• Make independent quality-related decisions based on regulatory and compliance knowledge and provide independent quality support to project teams
• Review and approve validation documents

• Degree in Biology, Chemistry, Biotechnology, Life Science or other related field or experience in the field of pharmaceutical industry
• Previous experience in GMP regulated pharmaceutical industry is an advantage
• English fluency and German good command is an advantage
• Ability to prioritize and manage work to critical project timelines in a fast-paced environment
• Excellent verbal, written and interpersonal communications skills

• A very renowned company
• A highly motivated team and an open way of communication

Ihr Kontakt

Referenznummer
781382/1

Kontakt aufnehmen
Telefon:+41 44 225 50 00
E-Mail: positionen@hays.ch

Anstellungsart
Freiberuflich für ein Projekt