Beschreibung
Quality Management Consultant (m/f)
Reference: -en
Start: asap
Duration: 6 MM++
Main tasks:
- Review overall SOP training assignments in the electronic training system with the functional areas and global quality management based on the local training curriculum
- Creation and revision of GMP/GDP relevant SOPs
- Coordinate review and approval of local SOPs with the functional areas and global quality management in the electronic document management system
- Investigation / assessment / follow-up of non-conformities (e.g. deviations, product quality complaints)
- Definition and follow-up of change controls and CAPAs.
Main qualifications
- Relevant work experience within the GMP area of a pharmaceutical Quality Management/Assurance function
- University degree in life sciences
- Knowledge/experience in relevant regulations and guidance documents (AMG, AMWHV, EU-GMP/GDP)
- Very good communication skills in English (written and oral)
- Open minded, good problem solving and resolution skills
- Well versed with MS Office
- Experience with electronic document management systems and Trackwise is of advantage
Main advantages:
- A young innovative company (as part of a global group with 39.000 employees)
- You will work in an international environment
- Good infrastructure
About us:
With over 15 years of experience in the pharmaceutical industry, 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 professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
My contact at Hays:
My contact person:
Jan-Niklas Seidel
Referencenumber:
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Email: