Validation Specialist

Role: Validation Specialist

Type: Permanent

Location: Lucerne, Switzerland

Rate: Competitive in line with skills and experience

For one of Planet Pharma’s global clients, a specialist life science consulting organisation we urgently seek several Validation Specialist to join on a permanent basis.

Responsibilities:

• Design and Execute Computerized System Validation (CSV) in accordance to GAMP 5 guidance – mainly on Analytical Laboratory Test Equipment and other Lab Information Systems
• Technical Writing of Validation Documents, IQ OQ PQ, Trace Matrix, Validation Summary Report), SOPs, Maintenance Procedures, Calibration Procedures, and other instrument support documents
• Translate technical information and requirements into qualification/validation test design

Requirements:

• Academic qualifications in a scientific focus subject
• At least 3-5 years’ experience within the pharmaceutical industry with additional validation experience
• Proven knowledge and experience of GMPs, 21CFR Part 11, USP 1058 – and other relevant industry regulations and guidance

To Apply

If you would like to discuss this vacancy further or to discuss your career options in confidence, please telephone on +44 (0)20 3928 6631 or email on mowusu-ansah@planet-pharma.co.uk

We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. Planet Pharma is an Employment Business providing Global Staffing services.