CQV Engineer - CIP Start up
12 month contract (potential of extension)
On site - Denmark

Our client currently has a team of CQV Engineers onsite who are responsible for providing cleaning validation 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 5-10 years experience in CQV, CIP start up and Cleaning Validation in a biopharmaceutical environment.

Responsibilities

• Lead the Commisioning and Qualification of CIP Skids
• 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.

• Experience of CIP skids and CQV is a must have for this role
• Minimum of 3 years’ experience in Commissioning and Qualification including CIP Start up
• Prior cleaning validation and CIP Start Up experience within bio-pharmaceutical industry is a distinct advantage
• 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