Validation Associate Specialist
- Company
- Planet Pharma Staffing Limited
- Location
- United Kingdom
- Salary
- Competitive
- Posted
- 26 Jan 2021
- Closes
- 25 Feb 2021
- Discipline
- Manufacturing, Process, Validation, Quality, Quality CSV Engineer, Quality Validation Engineer
- Hours
- Full Time
- Contract Type
- Contract
- Experience Level
- Experienced (non-manager)
Exciting opportunity to join a large and reputable company who pride themselves on employee satisfaction, progression and work environment. For more information apply to arrange a call!
Job Summary
Our client who is a market leading global bio-pharmaceutical company is currently looking to expand their QA team by bringing on a Validation Associate Specialist!
This position is perfect for someone who has some industry experience looking to work for a company who offer great progression, positive culture and great work/life balance.
Location: Office based in Luton area
Length: Initial 6 months + potential extension
FTE: 1.0 (37.5 hours per week)
Responsibilities
- Supervise validation testing performed by contractors to ensure work is accurately completed to the required standards
- Assists in developing programs and maintaining standard operating procedures (SOPs)
- Facilitation of the review and approval of validation documents.
- Generating validation technical reports related to systems, products and/or processes, in compliance with company standards and regulatory requirements
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.
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