Role: Validation Engineer - Pharmaceutical
Type: Contract, 3 Months+
Location: West Midlands
Rate: £45.00 - £55.00 P/H
An urgent contract requirement for an experienced Validation Engineer has become available with a leading pharmaceutical manufacturing business in the West Midlands.
The successful Validation Engineer will be responsible for day-to-day Validation System management and compliance.
Working with the Validation Leader you will be is responsible for establishing a close working relationship with Operations, Quality Control and Project Management to actively and effectively manage, optimise and develop the site Validation System, ensuring that GMP compliance is maintained at all times.
Management of the site Validation System in accordance with the Site Validation Master Plan – SVMP - to defined timelines.
Scheduling of programmes of Validation
Management and attendance of FAT and SAT as required.
Management of equipment, process and facility qualification status in accordance with SVMP in collaboration with Operations and QC.
Generation, review and approval of a wide range of documents, including, Validation Plans, URS, DQ, IQ, OQ, PQ, Validation Summary Reports, and maintenance of the SVMP.
Supporting the Quality Director in Regulatory and Client audit preparedness activities, hosting, audit response and action closure.It is essential that applicants have a proven background in GMP Validation from Pharma industry with a broad knowledge of pharmaceutical systems and/or processing equipment in relation to operation and qualification parameters.
Please send your latest CV to apply for this contract opportunity. Successful candidates should be available at short notice to start in this role.
Skills: Validation Engineer, Validation Lead, Equipment Qualification, GMP Qualification, Systems Validation, Process and documentation, GMP Suite, Pharmaceutical, Pharma, Medical Equipment
Product Quality Assurance