Description
Our global pharmaceutical client is looking for a cleaning validation engineer to support the transformation of a chemical site into a biomanfacturing facility. This role will work as part of the project team to support the review of cleaning validation processes and introduction of new equipmentJob Description
• Management of equipment qualification in QC including:
o Regular QC equipment maintenance and requalification
o QC equipment calibration
o Preparation of maintenance, calibration and qualification documentation
o Training of QC personnel in equipment qualification regulations
o Co-ordination of activities between QC and Engineering departments
• Support the introduction of new equipment
o Support the lab design process for the introduction of new equipment.
o Write relevant QC documentation for new equipment.
o Carry out qualification of new equipment.
Minimum requirements
• Strong experience of working in a laboratory environment, ideally on a biologics facility.
• Experience in writing and execution of qualification documentation for QC equipment.
• Experience in GMP regulated industries
• Excellent communication, interpersonal and training skills (French and English language).
• Proven ability to establish collaborative working relationships; team-oriented and must be able to work independently.
• Excellent ability to manage multiple projects and tasks.
• Personal attributes include flexibility, integrity, action- and goal-oriented.
Should you be interested to apply, please send your up to date CV and cover letter to