1 to 12 of 12 Permanent GxP Jobs in the UK excluding London

activities of the company in relation to QMS Compliance. To maintain awareness of existing and new legislation/guidance relating to EU and UK GXP for medicinal products and medical devices including all ISO activities relevant to medical devices including ISO 9001, ISO 13485 and ISO 14971; Controlled Drugs; Nutritional … Products; and General Data Protection Regulations and the UK Data Protection Act. What will you be doing? Maintaining Aspire Pharma Limiteds EU and UK GXP/ISO 9001/ISO 13485/ISO 14971 QMS, including: Staff training. Documentation control. Change control. Non-conformance/deviations. Validation. Corrective and/ more »

be beneficial to your application, but is not essential: Bachelors degree (or equivalent) in a scientific or technical discipline Worked within a pharmaceutical/GxP environment in a Quality related role Familiarity with the production of solid dose oral products Management of electronic & physical documentation systems Reward For the successful more »

to your application, but is not essential: HNC in Engineering or Construction (or equivalent). Previous experience within the pharmaceutical industry and working to GXP compliance. Experience using document control/maintenance management systems. Reward For the successful candidate, we offer an attractive benefits package which includes a competitive salary more »

conduct site visits to ensure project completion and right first time quality is driven. Work with internal team members cross-functionally Uses technical and GXP knowledge to influence and assure Quality and Compliance in Design and develops plans for New Product Development/Post Launch/lifecycle management activities. Act more »

Piramal Grangemouth and maintenance of Regulatory Registrations/Licenses/Certifications. The role will support the site and related functions in maintaining compliance with GxP regulations and applicable quality guidelines, including, but not limited to UK/EU/US GMP/GDP, ICH and other region specific guidance. The … documentation according to internal guidelines and UK/EU/US/ICH and other region specific guidance. Lead Quality Management Review meetings highlighting GxP areas of concern and working to support and track actions that are to be taken. Support quality related investigations, assist in the development and approval more »

do business. The Opportunity Dechra Pharmaceuticals are looking for an experienced auditing professional to join our manufacturing division on a remote basis. Support the GxP and Regulatory compliance of Dechra Products by developing audit systems which will ensure process and product compliance with applicable GMPs/GDPs throughout the product … lifecycle. Develop, approve, and monitor the risk based GxP audit programme and budget for Dechra DPMS. Develop and support inspection readiness at Dechra Internal Manufacturing sites, sustaining their ability to successfully conclude regulatory inspections for Dechra's products. Provide US and European regulatory intelligence, train Subject Matter Experts and provide … and review or preparation of responses to deficiencies) and on-site presence as required. Develop audit systems to ensure key elements of the Dechra GxP Quality Management System and the requirements of the product licences/marketing authorisations are effectively implemented throughout the internal and external manufacturing network (as required more »

RC&QA Leadership Team's delegate Perform other duties, as assigned by management Required profile: Required experience: 10+ years in regulatory environment (experience in GXP roles) Experience & regulatory expertise of industry quality systems/standards Ability to effectively communicate functional strategy with external parties Ability to effectively lead teams through more »

Manage, coach and mentor more junior members of staff. Provide clear scientific and technological leadership to direct reports. Comply with all relevant safety and GxP procedures. Plan and prioritise own, and team’s work with input from senior manager when required. Involve in CRO’s selection process. Provide an oversight more »

support in a team responsible for the delivery of the scientific and technical activities of the Immunoassay Group (IAG) and other groups within the GxP test facility when required. This post sits within the IAG Team. The successful candidate would be educated in degree level in a relevant subject area … of the application of serological assays to support clinical trials and/or product characterisation would be an advantage. Experience of working within a GXP environment is highly desirable. This post is not suitable for biomedical scientist accreditation. About us We pride ourselves as being an employer of choice, where more »

services (e.g. PTQA or Scientific Training Programme) or working towards. Experience Essential Experience of pharmacy manufacturing or other significant experience of working in a GxP environment Quality control and quality assurance experience including environmental monitoring. Experience of working within and maintaining a Pharmaceutical Quality Management System - Change Control, Deviation and … implementing changes as appropriate. Desirable Experience of participation in external audit and hosting external auditors. Experience of line managing personnel Experience of conducting internal GxP quality assurance audits Experience of project management of complex systems Skills Essential Good organisational and time management skills. Able to work independently and show initiative … constructively and deal with issues sensitively. Skill of managing personnel within teams In depth and practical knowledge of the legislation and standards relating to GxP, ability to apply this knowledge to develop and maintain a Pharmaceutical Quality Management System. Knowledge of clean room design and function and HTMs/HBNs more »

Pharmaceutical production or development environment, to include QC and working with staff on issues arising within a production environment. Familiar with the concepts of GxP systems and other pharmaceutical terms and acronyms. Experience of managing Tech transfers, troubleshooting and product development of product change projects including process, analytical, planning, documentation more »

procedures for the development lifecycle. Maintain in-depth knowledge of technical specialisms. Serve as a subject matter expert for architecture domain decisions. Comply with GxP requirements and standards using appropriate SOPs, methods, and tools. Perform additional duties as needed. Your Essential Criteria: BSc in Computer Science, IT, or related field more »