1 to 25 of 125 Permanent GMP Jobs in England

guidelines and methods ensuring quality guidelines are adhered to * Support in routine QA duties to ensure manufacturing and testing activities comply with the local GMP facility processes where products are manufactured * Day to day responsibilities include the following elements of the PQS relating to manufacture and testing of cellular therapies … continuous improvement within team What are we looking for? * Min 2 years’ experience or equivalent experience working in a Quality Assurance role in a GMP environment * Experience in providing pragmatic quality advice to manufacturing and quality control functions * Experience writing and reviewing GxP documents (including SOPs) to ensure good documentation … data integrity, GxP, quality and regulatory requirements are met. * Working knowledge of GMP relating to sterile production, cleanrooms, aseptic technique and hygienic requirements for sterile products is desirable * A working knowledge of regulatory requirements or processes that specifically apply for the manufacture and/or testing of cell therapy products more »

and expert teams as SME. Requirements • Scientific Degree or an equivalent in Chemistry, Biology, Pharmacy or Pharmaceutical Engineering. • Experience in quality operations in the GMP environment. • Knowledge and understanding of regulatory requirements. • Good knowledge of office tools (e.g. Word, Excel, SAP). • Interested candidates should submit an updated CV. Please more »

working. You will manage all company pension schemes and ensure that all legislative requirements are met. This role will involve project work, centred around GMP equalisation buy-in preparations and benefit changes. You will also manage the day-to-day administration of pension schemes. Responsibilities also include communicating and educating more »

who is adaptable, can show initiative and pick up lots of new skills quickly Good general laboratory experience, ideally with GLP and/or GMP certification (not essential) For the chance to join an exciting company on their journey to change the world for the better, please apply today! Bond more »

Senior Actuarial Analyst - GMP London £40,000 - £60,000 per annum Leading mid-sized consultancy in their search for a Senior Actuarial Analyst to join their actuarial technical team | Those wanting to stop or have stopped sitting actuarial exams will also be considered. Company client is working with a leading … mid-sized consultancy in their search for a Senior Actuarial Analyst to join their actuarial technical team with a focus on the delivery of GMP equalisation projects. Within this role, you will check technical calculations, provide technical expertise and support to client teams with a dominant focus on GMP work. … Although GMP work will be your main focus initially, over time this business will incorporate similar technical project work into your role as the demand for specific GMP work reduces. Role requirements: * Part-qualified actuary or technical equivalent skill-set with a desire to not. * GMP equalisation calculation experience, or 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 »

which will include some weekend working as set by the rota. Day to day duties will be: To audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence. Effectively communicating to enable the operational teams to take the appropriate and more »

of working within a Quality Assurance Officer role within a fast-paced environment. You should have at least 2 years' experience of working under GMP or have a degree within a science discipline. Knowledge and understanding of GMP with excellent communication and organisation skills are essential for this role. To … Society, Royal Society of Chemistry or Institute of Biology, GPhC, Science Council. Your duties & responsibilities The final review of pre-manufacture batch documentation, following GMP guidelines. The Approval for Use (final release) of all products manufactured or repackaged according to licensing requirements, GMP and professional discretion Being the primary point … attend any suitable training and update courses as deemed necessary and ensure a high level of competency is achieved. Ensuring that staff comply with GMP, COSHH and Health and Safety regulations and departmental SOP's. Participating in any rota system that may operate within the product release team in order more »

policies. To be proactive in identifying and eliminating faulty processes by implementing long-term fixes. To uphold and exceed standards of product quality and GMP within their area that are appropriate to an industry-leading quality food manufacturer. To play an active role in the shift and be the go more »

QA Auditors in monitoring and evaluating product and processing systems. Duties To 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 To ensure products and … Line Manager, manage QA activities required to deliver improvement of Technical KPIs e.g. audit of non-conforming processes, complaint investigations, update of swab schedules, GMP audits, glass and plastic audits. Lead, motivate and inspire QA team to achieve personal development and continuous improvement To promote a quality culture and help 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 »

focus: Actively participate in the implementation of site quality improvement projects, where necessary providing support to train operation teams and monitor project effectiveness. Complete GMP and Hygiene audits to required schedules. Assist in the investigation of consumer complaints and non-confirming items determining root cause and corrective action necessary to more »

area highlighting any stock issues to the engineering team manager To maintain standards of hygiene and good housekeeping appropriate to a quality food manufacturer. GMP standard of workshops and engineers tool boxes is maintained at a high level About you Strong people management experience A multi skilled background Experience completing more »

Material & Production Planning master data Prior knowledge of manufacturing, production planning & forecasting Have previous experience in a support environment Experience in companies manufacturing to GMP Standards Knowledge of SQL Experience in analytics/dashboarding more »

and equipment automationsystems at our Holmes Chapel site. You'll provide hardware and softwaresupport, resolve breakdowns, implement preventative maintenance, and ensurecompliance with GMP (Good Manufacturing Practice), EHS, and company standards.Your role also involves supporting computer system validation, qualityimprovement initiatives, and training other team members. This is a hands-onrole where … support to maintain system performance. Provide hardware,software, and coding support to maintain system performance. Resolve equipmentbreakdowns and conduct root cause analysis. Ensure compliancewith GMP, EHS, and company standards. Support computersystem validation and lifecycle management. Contribute toengineering best practices and project execution. Train team memberson equipment, systems, and procedures. Automation more »

satisfy the requirements of external agencies. Responsible for timely and accurate reporting of internal Refresco KPIs to the management team. Be responsible for ensuring GMP and Hygiene standards are communicated to the operational teams and processes are in place to effectively monitor and manage them. Partake in site visits and more »

to respond to change environments and high growth, high pressure environments. Experience in managing stakeholders. Ability to track and report issues. Experience & understanding of GMP, FDA & TGA Quality requirements. Culture & Benefits We are fuelled by our commitment to sustainability, quality, efficiency, and an unwavering passion for our customers. Championing solutions more »

and provide corrective action Use root cause analysis to understand and deliver optimal cost maintenance Delivery of the required standards in relation to Engineering GMP and food safety standards Escalate potential consequences to line manager where work may impact on product quality or safety Key skills & experience: Strong engineering qualifications more »

you will be responsible for testing and reporting laboratory activities to enable compliant, on time delivery of products to the customer whilst adhering to GMP standards. Your contribution will be the regular completion of on the bench testing of Asthma Inhalers (MDIs). You will be part of a quality 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 »

focus on compliance within a specific bakery, working with the teams to identify non-compliance and full engagement and support to ensure company processes. GMP and procedures are fully understood. Work with the bakeries to ensure compliance with relevant customer standards and codes of practice. Conduct physical factory audits (outside … safety and quality. Ensure that the Quality Management System internal audit schedule is completed, and all actions closed out in a timely manner. Ensure GMP & QA CCP audits are conducted to schedule and any non-conformances raised to bakery management. Verify that close out actions are robust and complete. Communicate more »

development with an understanding of the product life cycle ideally in laboratory automation, or pharmaceutical manufacturing environment following ISO/IEC and/or GMP standards though candidates from other industries will also be considered Hands on experience in electrical engineering in prototyping, engineering, design and testing Working knowledge of more »

work environment and that all tools are maintained and accounted for. Liaise with the SHEQ team to resolve H&S issues, environmental, internal audits, GMP, COSHH and ISO quality issues, and ensure all compliance checks are complete and correctly filled. Attend all nominated training modules as necessary. Undertaking any other more »

Desirable) Time served Engineer. NVQ Level 3 Qualification or above Electrical Bias The Role Carry out duties ensuring the site achieves and maintains required GMP standards. Ensure all work conforms to statutory & safety requirements. Ensure that risk assessments are completed and actioned. Carry out site maintenance activities and ensure GMP more »

Job summary The Good Manufacturing Practice (GMP) Unit at Guy's Hospital was formed to accelerate the translation of novel approaches to the prevention, diagnosis and therapy of major unmet diseases relevant to the NHS, and will ultimately contribute to the improvement of patient outcomes. Specialising in developing and manufacturing … cell and gene therapies for use in early phase clinical trials, the GMP Unit is looking to appoint a Advanced Therapy Quality Scientist. Main duties of the job The field of Advanced Therapy Medicinal Products is expanding rapidly; this post gives the prospective candidate the opportunity to expand their horizons … a Clean room. Desirable Experience in cellular immunology techniques such as proliferation, LDA, HLA-peptide multimers, cytokine secretion and ELISPOT assays Experience in Good Manufacturing Practice Skills Essential Ability to participate in the organisation of the laboratory Ability to develop novel QC assays and assess suitability Knowledge of: environmental monitoring more »