Description
One of the leading suppliers in the life science industry are looking to expand their contractor base and are currently recruiting for a Validation Engineer for an initial 6-month contract.The role would be based on the M4 corridor where the company have undergone a massive refurbishment and expansion at their facility and seem to keep growing.
The suitable candidate would be responsible for generation and execution of validation protocols and reports in line with cGMP, industry best practice and Lonza policy. You would need to plan your own work and work as part of the validation and wider team supporting GMP manufacturing and supporting functions.
Role and responsibilities:
- Responsible for the generation and execution of validation project plans, protocols and reports.
- Planning and managing the delivery of validation projects and procedures to meet current GMP regulations and guidelines, industry best practice and company policy.
- Formal review of validation protocols, reports and procedures
- Process and manage quality records including change control, deviation and CAPA.
- Has held multiple roles delivering validation projects within Biopharmaceuticals industry
- Experience working within a team
- Experience working in a GMP environment including clean rooms and facilities
- Good understanding of validation principles and a risk-based approach
- Good understanding of GMP in biopharmaceuticals
- Experience of Pharmaceutical quality systems including change control, deviation, CAPAs.
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