This Medical Device Manufacturing Client is looking for a Quality Specialist with 'batch release' experience to work at their Farnham site, although a perm role (with benefits) for 12 months, it comes with a 10% completion bonus. For this role, you would report to the QA Manager on site, and liaise with several other departments and Client sites. For this role you must have: * Working in a GMP environment making pharmaceutical products * QA batch release experience * Pharmaceutical quality system experience The primary responsibility of the role is to perform key quality activities relating to batch manufacturing documentation, customer complaint management and to support the Quality Assurance Function with overseeing the core quality system processes, therefore ensuring that quality standards and business needs are met at the site in Farnham. Responsibilities · To coordinate and maintain all activities required for the disposition of finished product by Qualified Persons. This includes partnering closely with manufacturing / operations team; diligent review of batch records for pharmaceutical drug products. · To review, check and approve completed batch and ancillary quality documentation to ensure compliance with GXP and assist the disposition of finished product by Qualified Persons. · Liaise with external contractors and third-party service providers regarding the review and approval of quality docume...