Lead CQV Consultant

Job Type	Contract
Area	Kildare, IrelandDublin, Ireland
Market	Life Sciences - Engineering
Currency	EUR
Start Date	ASAP
Advertiser	Nick Wild
Job Ref	SH-5696

Description: Daksta are looking for a Lead CQV Consultant for an 18-Month contract opportunity in Geneva. The Project is a large Pharmaceutical manufacturing facility.

Responsibilities

• Commissioning, Qualification and Validation of the project

• Documentation preparation of Commissioning, Qualification & Validation documentation

• Review of Contractor Handover Packages.

• Knowledge of regulations (ICH, ASTM, FDA, ISPE)

• Team management, working closely with the PM

Experience

• 15-20 years’ experience within the Pharma / Biotech industry, ideally with good exposure to managing projects in Switzerland

• Strong knowledge of the following –

• Upstream - Bioreactors 2000L (ideally single use)

• Downstream – Harvest Purification, 45cm Columns, buffer prep

• Utility systems

• Fluent French speaker

*The successful candidate must be fluent in French and have a high standard of written French as documentation being produced in French*

Needs full working rights within the E.U

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