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Our client, Global Manufacturers are currently seeking a Process Validation Scientist to be based at their site in the South West. Reporting to the Validation Manager, the main objective of this role will be to Produce Process Validation and performance Qualification Documentation according to site documented procedures as well as Customer and regulatory requirements.
You will be required to;
-Review Process and Analytical Development reports and other supporting documentation relating to the new products, or changes to existing products, or changes to existing products and assess their suitability for validation.
-Write PV protocols and reports, and PQ protocols and reports.
-Write or amend Batch manufacturing records as required when directly related to Validation activities.
-Co-ordinate with other departments with responsibilities for validation activities directly related to Process Validation and performance Qualification.
-Co-ordinate with Customers on Process Validation activities where required.
The preferred candidate will have pharmaceutical industry experience in Quality/Regulatory, production, Manufacturing or Validation. You will be highly organised with sound communication skills, and a proven ability to meet strict deadlines. A Science related HND or Degree would be desirable but not essential.
To apply for this Process Validation role forward your CV to mhall@redlineplc.Com or call Mel on 01614917831 for more information.
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