Northwich, Cheshire, North West, United Kingdom Hybrid / WFH Options
Dechra
Ensures that there are robust processes in place for the review and release product for GLP and GCP studies. Ensures appropriate quality oversight of GMP activities performed by the Product Development teams at Dechra or CDMOs and contract laboratories. This may include review and approval of protocols, reports, methods, master more »
operations of process development (PD) activities for Advanced Therapy Medicinal Products (ATMPs) in the London area. Additionally, the role involves supporting goodmanufacturingpractice (GMP) activities as needed, to enhance both existing and new ATMPs and contribute to the continuous improvement of the pipeline. Key Responsibilities : Process Development Management: Manage … and oversee daily PD activities in the London lab, GMP Support: Support GMP activities where required to facilitate the development and improvement of ATMPs. Collaboration: Work closely with the Lead of Process Development to expand PD capabilities within budget constraints. Project Development: Lead the development of new PD projects, focusing … on the commercialization of PSC RPE and the tech transfer of new ATMPs to GMP manufacturing. Documentation: Develop and maintain operating procedures and PD activity records to ensure accurate documentation for regulatory submissions for clinical trial approvals. Clinical Trial Support: Continue the development process as new ATMPs advance from early more »
Cardiff, South Glamorgan, Wales, United Kingdom Hybrid / WFH Options
Gyrus Medical Ltd An ATL Technology Company
the management and improvement of quality systems processes to ensure both EU and US regulatory compliance to relevant company standards and GoodManufacturingPractice (GMP). The successful applicant will: Implement and monitor established policies and procedures to ensure compliance with necessary regulatory bodies in the areas of: Corrective and … Work in accordance with Company Quality Standards, procedures and processes and comply with the requirements of Good Documentation Practice (GDP) and GoodManufacturingPractice (GMP). Deputise for Senior Quality Systems Engineer when required, to ensure progression of departmental commitments. We are looking for someone who has: Minimum A level … Directive MDD 93/42/EEC Knowledge of FDA QSR Part 820 Computer literate to include MS Word, Excel and MRP Knowledge of GMP and audits Ability to work with minimal supervision and use initiative. Good interpersonal skills and the ability to communicate well in English both written and more »
Cardiff, Wales, United Kingdom Hybrid / WFH Options
Gyrus Medical Ltd An ATL Technology Company
the management and improvement of quality systems processes to ensure both EU and US regulatory compliance to relevant company standards and GoodManufacturingPractice (GMP). The successful applicant will: Implement and monitor established policies and procedures to ensure compliance with necessary regulatory bodies in the areas of: Corrective and … Work in accordance with Company Quality Standards, procedures and processes and comply with the requirements of Good Documentation Practice (GDP) and GoodManufacturingPractice (GMP). Deputise for Senior Quality Systems Engineer when required, to ensure progression of departmental commitments. We are looking for someone who has: Minimum A level … Directive MDD 93/42/EEC Knowledge of FDA QSR Part 820 Computer literate to include MS Word, Excel and MRP Knowledge of GMP and audits Ability to work with minimal supervision and use initiative. Good interpersonal skills and the ability to communicate well in English both written and more »
Develop and implement comprehensive quality management strategies, policies, and procedures to ensure compliance with regulatory requirements (e.g. FDA, EMA, etc.) and industry standards (e.g. GMP, GDP, GCP). Provide leadership and direction to the quality assurance and quality control teams, fostering a culture of quality excellence, accountability, and continuous improvement. more »
Develop and implement comprehensive quality management strategies, policies, and procedures to ensure compliance with regulatory requirements (e.g., FDA, EMA, etc.) and industry standards (e.g., GMP, GDP, GCP). Provide leadership and direction to the quality assurance and quality control teams, fostering a culture of quality excellence, accountability, and continuous improvement. more »
Proactively address stakeholder concerns, resolve conflicts, and facilitate effective communication channels throughout the project lifecycle. Quality Assurance and Compliance Ensure compliance with regulatory requirements, GMP, and other relevant standards within the pharmaceutical industry. Implement robust quality assurance processes to monitor and evaluate project deliverables, ensuring adherence to specified quality standards. more »
City of London, London, United Kingdom Hybrid / WFH Options
Connect With Ltd
promoted internally. We need someone who has experience working in a Pharma/life science environment who has good knowledge of working in a GMP/GxP environment. This is a strategic role and requires someone who has previous regional experience with some auditing experience. The role is based from more »
pharmacy areas ensuring adherence to cGMP and Standard Operating Procedures Perform assessments during operations activities to ensure all work is performed in compliance with GMP, SOP and regulatory requirements Review cleanroom and supporting area documentation for accuracy and contemporaneous completion in batch records and logbooks Review executed batch records Proactively more »
as developing action plans to drive improvement. Your main accountabilities will include: Participate and direct QA team to observe and audit production processes and GMP, ensuring products are made to specification and within customer codes of practice and Bakkavor standards, reporting findings to managers as appropriate Assist in delivery of more »
Manchester Area, United Kingdom Hybrid / WFH Options
Factorytalk
have requirements: 2-5 years’ experience working with MES/EBR or similar systems in the life sciences industries. Experience deploying MES in a GMP environment, configuring Recipes, MBR’s, Materials, BOMs, Order Management, Equipment management, Batch Review/Approval and other typical components. A background in one or more more »
staff on quality protocols. Responsibilities: Develop and improve quality assurance policies and procedures to ensure compliance with regulatory requirements and industry standards (e.g. BRC, GMP) Conduct regular audits and inspections of laboratory and manufacturing processes, equipment, and documentation to identify areas for improvement. Gain expert knowledge of the business management more »
Undertake other duties in relation to the position as the Company requires, including working additional hours as requested by the Systems Delivery Manager Ensure GMP is adhered to in all areas of work. Understand Company’s Health & Safety Policy and follow all company HSE procedures.Report all accidents or any unsafe more »
and relevant experience within a food/drink or pharmaceutical industry, including experience working within a quality function. A thorough knowledge of FDA, MHRA, GMP requirements, auditing and legislation is desirable. Other essential behaviours are the ability to work independently, good communication, facilitation skills and attention to detail. This is more »
business case for new R&D developments. Regulatory Intelligence: Maintaining awareness of existing and new legislation/guidance relating to ensuring developments comply with GMP/GDP/GCP and GXP, HMR, MDD and MDR where applicable. Quality Policy: To maintain an awareness of, and compliance with the company Quality more »
Learn about the Danaher Business System which makes everything possible. The Quality Control Technician Supervisor is responsible for ensuring adherence to GoodManufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills more »
Learn about the Danaher Business System which makes everything possible. The Quality Control Technician Supervisor is responsible for ensuring adherence to GoodManufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills more »
Learn about the Danaher Business System which makes everything possible. The Quality Control Technician Supervisor is responsible for ensuring adherence to GoodManufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills more »
Learn about the Danaher Business System which makes everything possible. The Quality Control Technician Supervisor is responsible for ensuring adherence to GoodManufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills more »
Learn about the Danaher Business System which makes everything possible. The Quality Control Technician Supervisor is responsible for ensuring adherence to GoodManufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills more »
Learn about the Danaher Business System which makes everything possible. The Quality Control Technician Supervisor is responsible for ensuring adherence to GoodManufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills more »
Learn about the Danaher Business System which makes everything possible. The Quality Control Technician Supervisor is responsible for ensuring adherence to GoodManufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills more »
Learn about the Danaher Business System which makes everything possible. The Quality Control Technician Supervisor is responsible for ensuring adherence to GoodManufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills more »
Learn about the Danaher Business System which makes everything possible. The Quality Control Technician Supervisor is responsible for ensuring adherence to GoodManufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills more »
Great Ormond Street Hospital for Children NHS Foundation Trust
manufactured at GOSH as a named person on the licence . In particular the quality assurance service provides support to ensure the delivery of GMP across the MHRA-licensed pharmacy production service, the delivery of GDP in the MHRA-licensed pharmacy distribution service and the delivery of GCP related to more »