Validation Engineer
View: 102
Update day: 01-06-2024
Category: Quality Assurance / Quality Control
Industry: Medical Equipment Manufacturing Biotechnology Research Pharmaceutical Manufacturing
Position: Associate
Job type: Full-time
Job content
Experience of validation within a highly regulated business?
Looking for a permanent position within an exciting and growing business?
We are working with our client on a retained basis, who, due to ongoing growth, are looking for a Validation Engineer to join them on a permanent basis.
My client, who are based in the Cambridge area are in need of a Validation Engineer to be responsible for validating and qualifying the systems and equipment used to develop and/or manufacture their sterile products in accordance with cGMP regulations.
Key responsibilities:
• Take part in or lead various validation activities
• Prepare validation and performance qualification protocols for new equipment
• Revalidation of new and/or existing manufacturing equipment and support systems
• Develop, prepare and install new equipment
• Revise test validation protocols and procedures where required
• Coordinate on projects with service providers to ensure all validation and installation requirements are being met
• Create, populate and maintain databased for tracking validation activities
This is an excellent opportunity to join a business that are in a healthy growth phase that can offer a supportive, mature and collaborative working environment
Harris Lord are working as a Recruitment Agency in relation to this position
Deadline: 16-07-2024
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