C&Q Engineer (m/f/d)

REFERENCE NUMBER:

613955/1

MY DUTIES:

- Write/review Qualification/Validation plans, including but not limited to DQ, IQ, OQ, PQ plans/protocols and final reports for new or modified GMP utilities, facilities, and process equipment
- Execution of DQ, IQ, OQ, PQ, including protocol deviations, investigation, and corrective action activities for new or modified GMP utilities, facilities, and process equipment
-Plan and track execution of Commissioning & Qualification activities/documentation versus project(s) timeline
- Prepare, review and approve technical and GMP related documentation (URS, FMEA, impact/risk assessment, Master plans, qualification/validation documentation)
-Coordinate and execute FAT/SAT, commissioning activities for new GMP systems in collaboration with internal and external partners
-Coordination and oversight of external suppliers

MY QUALIFICATIONS:

- Bachelor/Master’s degree in technical or natural sciences
- Working experience within pharma company in C&Q/CQV equivalent position
-Know-how of Qualification requirements according to cGMP regulations
- Experience working with ISPE baseline guide vol 3, vol 4 and vol 5 is a plus
- Business fluency in English, German language is a plus

MY BENEFITS:

- Dynamic and innovative market environment
- You will work in an international environment
- Varied tasks in a renowned company

ABOUT HAYS:

Our many years of recruitment experience and our expert knowledge of the engineering job market make us a strong partner for engineers and technicians. We maintain close relationships with customers across all industries and therefore can provide engineering specialists with exciting projects and attractive job opportunities, drawing on your personal interests and experience. As your professional companion, we support you throughout the entire process, from the first contact to the first day on your new job – all this completely free of charge. Register now and look forward to many interesting and suitable positions and projects.