4 of 4 GMP Jobs in the North West

activities (IQ/OQ/PQ) for equipment and processes Ensure timely delivery of KPIs and departmental objectives The Person Proven experience within a GMP-regulated environment in a similar QA/Validation role Experience in equipment validations (writing reports), the ideal applicant will have process validation experience too Previous ...

product investigations Coordinate and resolve immediate/urgent customer complaints, ensuring prompt responses/resolution Participate in the internal audit programme to ensure continued GMP compliance of all site activities Utilise scientific resources in order to work on improving quality of products and services To maintain personal training folder … Controls CAPAs Deviations Complaints Recalls OOS/OOT The Person: Will have a Degree in a relevant- Scientific discipline Will have good knowledge of GMP Experience in CAPA, Deviations, OOS, OOT, Internal auditing (preferred), Customer Complaints handling would be very advantageous Strong IT skills (Microsoft applications) Good interpersonal skills ...

client, a growing pharmaceutical organisation, is seeking a Quality Systems Officer to join their Quality team. This is an excellent opportunity for someone with GMP experience looking to develop their career within Quality Assurance and Quality Systems. Key Responsibilities: Supporting the day-to-day maintenance of the Quality Management System … Assessments Assisting with internal audits and audit readiness activities Supporting customer complaints, investigations and quality records management Maintaining training records and ensuring compliance with GMP requirements Participating in continuous improvement initiatives across the business Experience Required: Degree qualified in a Scientific discipline (preferred) Previous GMP experience within Pharmaceutical, Biotechnology ...

more than a "keep the line running" position, it's heavily involved in automation, system setup, validation and continuous improvement within a GMP-regulated setting. The Role You'll play a key role in delivering and supporting automated manufacturing systems across the site, working closely with engineering, projects and operations … platforms Leading and supporting capital projects from concept through to validation Developing technical documentation including SOPs, specifications and validation protocols Supporting GMP compliance, change control and validation activities (IQ/OQ/PQ) Troubleshooting and resolving process control and automation issues Supporting new product and technology introduction from an engineering ...