Description
CQ Documentation Preparation Lead 100% (m/f/d)
Reference: -en
Start: asap
Duration: 12 MM
Main tasks:
- Ensure documentation consistency across the CQ group and manage COMOS / KNEAT / DMS interfaces for CQ group
- Responsible for documentation management for the project CQV group. Creating templates, first-of-kinds, alignment across group, approval process, retention process, etc.
- Coordination of Operational Qualification Protocol preparation and approvals, including release for OQ and PQ
- Coordination of GMP regulations and management of the training programme for Commissioning and Qualification activities
- Coordination and communication with other resources for Qualification / Documentation Management activities
- Self-manage CQ development review / approval activities with respect to COMOS/KNEAT platforms
Main qualifications
- Bachelor’s degree in Life Sciences or Engineering
- Solid experience in commissioning / qualification / validation (DQ, IQ, OQ, Commissioning) activities in the pharmaceutical/biotech industry
- Fluent English language written and verbal communication skills
- Experience with COMOS/KNEAT platforms
- CGMP knowledge and knowledge of regulatory requirements
Main advantages:
- Challenging and varied tasks in a promising and innovative industry
About us:
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.
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