Validation Leader

ETR are supporting an leading Scandinavian engineering consultancy that require a  Validation leader for the pharmaceutical industry on a long term contract basis:

Assignment Description
Our client is looking for an experienced validation leader who wants to collaborate with us for assignments with our customers in the pharmaceutical industry. You are responsible for leading, planning and implementing validation activities. You can be expected to lead and coordinate a group of validation engineers. That includes planning; documentation, report and execution of IQ/OQ/PQ, VP or VMP.

Job description

The work can be expected to be carried out in one of the following areas:

• Analysis equipment QC lab (e.g. in new construction or reconstruction)
• Whole Production Line
• Computerized Systems
• Production Equipment
• Test

In your application, state what you have the most experience with.
 

Properties:
Communicative, driven and meticulous are the most important qualities. You like to plan and document as well as to keep track of several things at the same time. It is important that you are good at collaborating in a team.

Qualifications:
You have a university degree/Master of Science in Engineering in biotechnology, biochemistry, chemical engineering or similar that is considered equivalent. Experience from GMP and the pharmaceutical industry is a requirement.