Stellenangebot: USP Bioprocess Engineer (m/f/d)

Über uns

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.

Aufgaben

• Develop, enhance, and implement documentation systems to optimize production and service processes in a GMP-regulated environment
• Independently review manufacturing and cleaning batch records in accordance with internal SOPs and ensure timely completion
• Participate in cross-functional review meetings with QA and production teams to ensure compliance and continuous improvement
• Maintain and update documentation lists (e.g. KPIs, issuance logs) and support production teams with document preparation and archiving
• Create production certificates upon batch completion and manage controlled copies of work instructions
• Evaluate existing documentation processes and propose improvements to increase efficiency, quality, and compliance
• Provide general documentation support to project teams, including label checks, document collection, and prototype testing
• Support administrative tasks such as presentation creation, office supply orders, and document archiving

Profil

• Solid experience in a pharmaceutical or GMP-regulated environment
• Completed vocational training or equivalent professional qualification
• Strong understanding of current cGMP regulations and documentation standards
• Excellent written and verbal communication skills in English; German is advantageous
• Proficient in MS Office and digital documentation systems
• Detail-oriented with a structured and reliable working style
• Ability to organize daily tasks independently and ensure timely completion
• Communicative and a strong team player

Wir bieten

• Work in a high-impact role within a regulated and innovative pharmaceutical setting
• Close collaboration with QA and production teams
• Opportunities for professional development in process optimization and documentation systems

Ihr Kontakt

Referenznummer
847862/1

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

Anstellungsart
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