Validation Co-ordinator - API Pharmaceutical

Switzerland  ‐ Onsite
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Keywords

Description

An excellent opportunity has arisen to work in Switzerland for an experienced Validation Co-ordinator (English Speaking). This is an exciting & interesting role for someone with excellent communication skills & vibrant personality to help co-ordinate the validation engineering teams on site.

Working for a top 5 Pharmaceutical client, currently undergoing a number of upgrade & revamp projects within an API environment, we are looking for someone with technical knowledge of chemical API production processes & equipment such as driers & centrifuges.

Role and Responsibilities:
• Co-ordinate the planning, execution and reporting of all qualification activities on the refurbishment of an active pharmaceutical ingredients’ (API) production facility
• Matrix management of the engineering team that will be carrying out the execution of the qualification protocols
• Review and approve the IQ/OQ protocols to ensure that these comply with GMP and internal guidelines
• Ensure that all qualification activities are closed out in a timely manner

Requirements:
• Degree educated in Chemical Engineering, Process Engineering or Mechanical Engineering
• Experience in the planning and execution of qualification activities on pharmaceutical production facilities according to GMP
• Technical knowledge of chemical API production processes and equipment

This is a contract opportunity with the likelihood of extension, due to the vast number of ongoing projects. Call me now for further details.
Start date
n.a
From
Quanta Consultancy Services
Published at
30.07.2014
Contact person:
Lee Mitchell
Project ID:
750371
Contract type
Permanent
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