Beschreibung
CQV Engineer (m/f/d)
Reference: -en
Start: asap
Duration: 7 MM++
Main tasks:
- Plan, coordinate and execute all phases for qualification of GMP manufacturing systems including but not limited to Qualification/Validation plans, FMEA, DQ, IQ, OQ, PQ
- Prepare, review and approve technical and GMP related documentation (URS, impact/risk assessment, Master plans, qualification/validation documentation)
- Coordinate and execute FAT/SAT, commissioning activities for new manufacturing systems in collaboration with internal and external partners
Main qualifications
- Bachelor or Master degree in technical or natural sciences
- Profound working experience within pharmaceuticals, biotechnologies or chemical industry
- Know-how of commissioning and qualification requirements according to GMP regulations
- Experience in quality assurance principles and working with cross-department stakeholders
- Know-how of ISPE baseline guide vol 3, vol 4 and vol 5 is beneficial
Main advantages:
- A highly motivated team and an open way of communication
- You will work in an international environment
About us:
Our many years of recruitment experience and specialist knowledge of the engineering job market make us a strong partner for engineers and technicians. We maintain intensive relationships with customers across all industries and so can provide engineering specialists with exciting projects and attractive job opportunities. Whether it's working with an international automotive manufacturer or a regional market leader in mechanical engineering, drawing on your interests and experience, we will find the right job to suit you. Because with us, specialists find their ideal working environment – 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:
Jonas Jakob Unkrig
Referencenumber:
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