1 to 3 of 3 Permanent Validation Jobs in Suffolk

monitoring of funding requests for NHS payment scheme excluded medicines and medical devices. This will include the management and processing of prior approvals, invoice validation and development and maintenance of monitoring systems. The job description and person specification are an outline of the tasks, responsibilities and outcomes required of the more »

PM Group is seeking a Validation Engineer to join an API Manufacturing facility in Suffolk for 3-4 months. Responsibilities: Work closing with Capital Project, Production, QA, and R&D departments to get the validation scopes and agreements to release the desired production status in the agreed timelines. Weekly update … to report the progress status of the validation works. Update and draft the required validation documentation, including but not limited to CSV/CQV validation protocols, VP, C&QP, SIA, URS, DRR/VRA, IOQ, OCD, C&QR, RTM, and VR. Execution and approval of the corresponding protocols to release … the required equipment for GMP production Weekly Validation Report Draft, execution, and approval CSV/CQV validation protocols Qualifications & Requirements: Applicants will have experience of general validation on multiple projects in the pharmaceutical and/or biopharmaceutical sectors. Working with other departments and key stakeholders Good communication skills and be more »

the on-going success of this ever growing business. DUTIES & RESPONSIBILITIES: Oversee the commissioning process for new repeat-build machines. Supervise the installation and validation of upgrades on machines. Document Overall Equipment Effectiveness. Develop and update related documentation. Manage and revise logs of machine settings and modifications. Analyze machine performance more »