1 to 25 of 154 Permanent GMP Jobs

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 good manufacturing practice (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 »

the management and improvement of quality systems processes to ensure both EU and US regulatory compliance to relevant company standards and Good Manufacturing Practice (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 Good Manufacturing Practice (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 »

the management and improvement of quality systems processes to ensure both EU and US regulatory compliance to relevant company standards and Good Manufacturing Practice (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 Good Manufacturing Practice (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 »

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 »

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 »

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 »

Safety at work regulations. * Carry out all tasks in a safe and controlled manner, adhering to quality requirements. * Consistently comply with Good Manufacturing Practices (GMP) and act as a role model for others on site. * Understand product safety and customer-specific requirements, and help ensure they are always met. Senior 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 »

SOF) Experience in hosting GCP Inspections Experience in IT Systems validation desirable Experience in implementation of general data protection regulations desirable Operational knowledge of GMP, knowledge of GLP and GCLP desirable Northreach is an equal-opportunity employer and we do not discriminate against any employee or applicant for employment based more »

Learn about the Danaher Business System which makes everything possible. The Quality Control Technician Supervisor is responsible for ensuring adherence to Good Manufacturing 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 Good Manufacturing 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 Good Manufacturing 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 Good Manufacturing 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 Good Manufacturing 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 Good Manufacturing 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 Good Manufacturing 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 Good Manufacturing 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 Good Manufacturing 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 Good Manufacturing 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 »

monitoring good manufacturing practices, applying HACCP principles and preventing reoccurrence of non-conformance against these standards. To audit compliance against Quality Management Systems and GMP, raising all non-conformances against relevant standards with objective evidence enabling the operational teams to take the appropriate and necessary corrective action, to follow up more »