12 month contract (potential of extension)
On site - Denmark
Steam In Place Experts

We are looking for a team of CQV Engineers with experience in SIP onsite who are responsible for providing expertise to support on site facility design, start-up and routine commercial manufacturing.

The ideal candidate would have 5-10 years experience in SIP start up and extensive CQV experience in a biopharmaceutical environment.

Responsibilities

• Prioritize CQV 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.

• Minimum of 5-10 years’ experience in SIP Start up
• Experience of CIP skids and CQV is beneficial
• 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