1 to 19 of 19 Permanent GMP Jobs in London

team members on best practices and ensure compliance with regulatory standards. Conduct gap analysis, review change controls, and develop revalidation strategies as needed. Ensure GMP, Data Integrity, and GDP compliance, including timely training. Key Competencies: Proven track record in delivering regulatory-compliant validation strategies. Strong understanding of GxP compliance requirements. more »

products reach every corner of the globe with precision and efficiency. Be the guardian of quality, ensuring every launch meets the gold standard of GMP and GDP regulations. Tackle challenges head-on, turning obstacles into opportunities for innovation and growth. Keep stakeholders in the loop with your expert communication skills … Business, Life Sciences, Engineering). Strong experience in the pharmaceutical realm, where you've honed your project management skills. A deep-seated understanding of GMP and GDP guidelines. A proven track record of launching products would be advantageous. Great communication skills, coupled with the ability to navigate complex challenges with more »

to our customers through timely response and effective communication. * Ensuring Engineering standards are maintained, compliant with all legal requirements and factory standards and procedures (GMP, HSE and Process, etc.) are adhered to. * Liaise with department streams through meetings, understanding issues and setting plans to resolve. * Drive PPM's completion to more »

What you'll be doing: Lead on the delivery of assigned projects and scheme events Review the work of Pensions Data Technicians and provide feedback and technical support Regularly review the effectiveness and efficiencies of existing systems and controls and more »

probes, ph probes, etc.). Label verifications. Verify finished product labels and crate/case end labels to ensure correct Use By Dates. Complete GMP & Hygiene Audits. Completing of Daily/Monthly/Quarterly Glass & Hard Plastic Audits. Micro sampling to site schedule and manage an ongoing shelf-life library more »

you a skilled technical assistant with a passion for food manufacturing? Do you have a keen eye for systems and specifications, and experience in GMP and supplier approval? If so, we have an exciting opportunity for you! About the Role: We are seeking a Technical Assistant for our esteemed client … maintaining high standards and ensuring compliance with industry regulations. Key Responsibilities: Manage and maintain technical systems and specifications. Ensure compliance with Good Manufacturing Practices (GMP). Conduct supplier approval processes and audits. Collaborate with various departments to ensure seamless production and quality control. Provide technical support and expertise where needed. … Requirements: Proven experience in a technical role within food manufacturing. Strong understanding of systems and specifications. Knowledge of GMP and experience in supplier approval processes. Excellent attention to detail and organizational skills. Must have an indefinite right to work in the UK. Why Join Us? Competitive salary up to more »

provide Self-inspection report/Self inspection CAPA reports. Inform appropriate internal departments on audit results and work with the necessary staff to achieve GMP &GDP compliance. Ensure the implementation of corrective actions that are raised by deviations, internal audit, or regulatory inspection. Provide Navision and Nice label support. Support …/RA Manager Participate in QA/RA projects as and when requested. Skills & experience Previous min. 5 year experience within a Pharmaceutical Industry, GMP/GDP environment and Quality Assurance Proven experience working in quality control/assurance and/or regulatory assurance Proven experience in Quality Management Systems more »

for scaling up and down of bioprocess operations. - Understanding of how to develop and optimise processes for the purification of biopharmaceutical products. - Understanding of GMP and QbD considerations in a large scale manufacturing environment. - Understanding and experience with statistical and modelling software and tools. - Understanding of in-process assays such more »

Lead best practice in the department and become a key contact for the mentoring and training of more junior members of staff. Act as GMP ambassador, take responsibility for ensuring GMP compliance and adoption of GMP principles e.g., right first time. Lead activities to ensure close working with Analytical development … understanding of cell biology and immunology (preferred) Strong verbal and written communication skills. Flexible, self-motivated, and focused on team outcomes. Strong understanding of GMP regulations. Excellent organisational skills with the ability to present results clearly and logically, working co-operatively as part of a team, as well as independently. more »

data feed. Due diligence on new business transactions. Requirements: Qualified Pensions actuary with experience within a top consultancy or relevant firm. Strong understanding of GMP equalisation, Longevity Swap or risk transfer. Excellent stakeholder skills and ability to lead/drive projects. A tenacity to 'get stuff done' and find ways more »

Proclinical is seeking a dedicated individual for a Director of Quality Assurance position. This role is integral to our mission of developing solutions for some of the most crucial scientific challenges of our age. The successful candidate will be a 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 »

retrieve information from the Council’s various computer systems. Knowledge of current LGPS issues and legislation including but not limited to the McCloud judgement, GMP Rectification, reporting requirements and dispute resolution procedures Minorities, women, LGBTQ+ candidates, and individuals with disabilities are encouraged to apply. Interviews will commence next week, so more »

build brighter futures for colleagues, clients and communities. The role will form part of the projects team with the current focus being around delivering GMP Equalisation projects on the proposition to clients, which can incorporate or lead onto being involved in de-risking projects for clients over time. This is … with internal teams to deliver a streamlined service to other lines of business. Directly involved with the management of more junior colleagues within the GMP Equalisation team, including supporting with performance reviews, training, and personal development plans. Develop skills to support on various consulting aspects of GMP projects and have … in Pensions, with a focus on Technical aspects and solid exposure to consultants and broader client support teams. Experience of technical calculations required for GMP Rectification and Equalisation projects. more »

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 »

research organisations (CROs), staff an patients in accordance with current UK Clinical Trials Regulations and all amendments, Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) guidelines and department procedures. The postholder will support the pharmacy set-up, maintenance, delivery (including dispensing) close-down, archiving and invoicing … include the following: To maintain and support the Pharmacy Clinical Trials service in accordance with current UK Clinical Trials Regulations and all updates, GCP, GMP, GDP guidelines and departmental procedures Performing the operational set-up of all new clinical trials. Day-to-day IMP management activities including shipment receipt, accountability more »

support the Pharmacy Clinical Trials service in accordance with current UK Clinical Trials Regulations and all amendments, Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) guidelines and department procedures, ensuring the provision of a high-quality service to non-commercial and commercial sponsors, clinical trial units … literate and ability to use MSOffice applications e.g. Word and Excel Demonstrates good general clinical knowledge and skills Demonstrates basic knowledge and understanding of GMP Effective pharmaceutical skills Understanding of clinical risk and clinical governance Identifies own training needs and maintains a portfolio of practice Desirable Knowledge of basic IMP 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 »

Haematology wards Lead on and develop elements of the clinical pharmacy service to improve the patient experience. Provide release of chemotherapy products according to GMP Facilitate and promote rational and optimal medicines usage Provide assimilated and relevant medicines information to healthcare professionals and patients To participate in the out of more »