C&Q Engineer - Stability Chambers/Temp Mapping - Denmark

Description

Global Biopharmaceutical Manufacturing facility based in Denmark have a contract opportunity for an experienced Commissioning, Validation & Qualification Engineer.

Joining a busy manufacturing plant with a number of on going projects onsite, including expanding existing manufacturing capability and a new build project we are looking for candidates with previous Biopharmaceutical/Pharmaceutical GMP experience who can carry out the following:-

Role scope:

• Preparation of commissioning, IOQ validation protocols, Comm./OQ field testing for temp controlled chambers, (eg stability chambers, chamber mapping, - KAYE loggers, alarm testing), deviation handling, report writing etc.
• 2-4 years C&Q experience (documentation, execution).
• High GMP and Quality understanding and levels.
• Strong commitment, dedication and drive to succeed.
• Outgoing personality and willingness to contribute to a highly effective team where the work morale is very high!

This is an exciting opportunity to join a fast paced and friendly project with the scope to move onto further expansion projects

Candidates must work through a compliant payroll solution for this project.