Beschreibung
C&Q Manager (m/f/d)
Reference: -en
Start: asap
Duration: 24 MM
Main tasks:
- Report to GES Project Manager and C&Q SME as applicable on technical, scheduling and compliance standards
- Delivery of the C&Q effort to meet schedule, standards and procedures
- Plan, schedule and coordinate C&Q deliverables for the project (Deliverables include: C&Q execution plan, GMP Design review, DQ, FAT, SLIA, CLIA, RTM, TOP, SAT, IOC, IOQ
- Coordinate the C&Q execution including oversight on technical change control, deviation management, document control and C&Q training
- Lead, coach and support daily activities for the C&Q team
- Support the development of the required C&Q documentation and associated technical review of specifications
- Support inspection at vendor sites, detailed GMP reviews, supervision of installation on site installed by construction team and co-ordinate the start up with associated teams
- Work closely with the Technical SME to provide the technical guidance to team to ensure compliance, upholding GES and MSD standards of excellence in design, document generation and execution
Main qualifications
- Relevant pharmaceutical experience
- Previous profound procedural experience
- Good knowledge of English and German
Main advantages:
- Project experience within a renowned pharmaceutical group
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:
Lisa Wahrlich
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