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CQV Engineer

Telefoon contactpersoon:
+353 21 485 7200

Bedrijfssectoren:
Life Sciences

E-mail contactpersoon:
noreen_daly@oxfordcorp.com

Job Description:

We are looking for a CQV engineer to carry out the commissioning and qualification of new and modified process equipment. These new and modified installations are necessary to be able to produce a new product at the Sanofi Geel site.

Responsibilities:

In this position you will work in a project environment and you will be responsible for commissioning, qualification and validation of process equipment and utilities. Activities are carried out according to predefined procedures, standards and current CGMP legislation

Skills Required:

Service tasks:

• Drawing up user requirements together with system owner
• Carrying out risk assessments
• Drafting, approval and implementation of protocols and reports
• Perform FAT and SAT testing
• Carrying out commissioning and qualification tests (e.g. installation tests such as P&ID walk down, welding check, IO tests and functional tests, electrical schemes walk down)
• Reporting and following up on deviations, solving technical problems
• Follow-up of changes via the applicable project change control procedure
• Follow up on changes in own domain and communicate them to the relevant functions
• Overseeing activities performed by third parties
• Profile:
• We are looking for CQV profiles with at least 3 years of experience in C&Q
• Knowledge of cGMP in a regulated environment is a must
• The position requires daily interaction with other project team members (system owner, project engineer, ...), so we are looking for team players with good communication skills.

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