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Details

CQV Engineer - SIP Start Up


Reference:AMC1234 Location: Denmark
Qualification:DegreeExperience:See description
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: EHS Engineer, Validation Specialist

12 month contract (potential of extension)
On site - Denmark
Senior CQV Engineer - SIP Project


Our client currently has a team of CQV engineers onsite who are responsible for providing C&Q expertise to support on site facility design, start-up and routine commercial manufacturing. We are currently recruiting for additional support for this team in Denmark.

The ideal candidate would have 10-15 years experience in CQV including SIP start up experience in a biopharmaceutical environment.

Responsibilities

  • Prioritize cleaning verification/validation activities in line with the project schedule to ensure product submission timeline is met, and regulatory approval attained site wide.
  • Ensure project related work is carried out in accordance with the requirements of the clients validation policies, guidelines, validation plans and GMP.
  • Provide on the floor support for troubleshooting cleaning verification/validation related issues and to lead manufacturing investigations into process deviations.
  • Generation of reports / analysis of data against pre-determined criteria to GMP standards.
Knowledge and Skills
  • Minimum of 8 years’ experience in CQV and SIP Start up within bio-pharmaceutical industry
  • Possession of interpersonal, team work and communication skills
  • Demonstrated track record in the delivery of goals and improvements
  • This role is open to candidates from EU and UK
  • Desire to relocate or travel

Apply today or get in touch with Angela McCauley for more information!