51 to 75 of 124 GMP Jobs in the UK excluding London

fixed weekly rotation. Responsibilities: Perform routine quality control examinations. Conduct routine analysis of raw materials and products using various techniques. Ensure all work is GMP compliant. Use a variety of instrumental and wet chemistry techniques to ensure analysis is accurate. Ensure consistent production of high-quality self-care products. Key more »

corrective actions Collecting micro-samples as per schedule Traceability Investigations into complaints Daily auditing of CCPs Daily label checks Calibration Auditing of processing records GMP/fabric audits Temperature checks Quality checks The nature of this role requires a flexible approach to working hours. Core working hours are: Monday to more »

safety and legality can be assured and that all the necessary information is accurately recorded and retained The Position: Carry out Daily/weekly GMP audits as required. To complete a detailed shift report at the end of every shift. To audit daily process documents including monitoring weights on line more »

on a permanent basis. The Validation Manager will be leading the validation function to be able to execute report activities within the framework of GMP - Annex 11 & 15 in compliance with QMS requirements. In addition, they will be supporting multiple validation projects, liaising with the project departments and the associated more »

in using industry-standard software lifecycle management tools such as Jira, Confluence, and AHA! Previous exposure to applying industry compliance and quality standards (GLP, GMP, 21CFRPart11) in software products. Effective communication and stakeholder management skills to facilitate seamless collaboration and alignment across diverse stakeholders. If you possess a passion for more »

Search knowledge and experience with up-to-date certifications (Google and Microsoft ads). Understanding of bid management and core PPC platforms (Google Analytics, GMP platform, SA360 or Skai). Analytic mindset and an affinity for numbers. At least one year of PPC experience (ideally from an agency background). more »

Manager in the Process Engineering department. You will ensure that operations are performed in accordance with the requirements of company standards, industry standards, and GMP/GDP guidelines. Whats on offer? Excellent Salary & Benefits: You will receive compelling salary DOE, along with an exceptional benefits package. Innovative Leadership in Automation more »

background and ideally Team Leading people working on similar projects as listed below:- Skills and experience:- - Pensions Data Transfer - Client Onboarding - Implementation - System Configuration - GMP - BIBO - Buy in - Buy out - Pension projects Unique culture, fully diverse and inclusive, very supportive, with ability to grow and become senior manager. Responsibilities: Takes more »

the team's size and operational scope. Key qualifications: Extensive experience in Quality Assurance across diverse responsibilities Preferably, a background in pharmaceuticals, though other GMP environments will be considered Bachelor's degree or equivalent in a relevant technical field Strong proficiency across various quality functions such as batch review, investigations … into a senior leadership role within a fast-paced pharmaceutical environment, apply now to become part of a dedicated team. Keywords: Quality, QA, assurance, GMP, manufacturing, distribution, packaging, CDMO, pharmaceutical, batch release, systems, compliance, regulatory, specialist, investigations, CAPA, deviation, change control, operations, senior, leader, supervisor, manager, coach, mentor. more »

standards and key performance indicators. Support sensory activities: taste panels, sample preparation, sample collection, sample submissions, processing of results. Adhere to good manufacturing practices (GMP), good laboratory practices (GLP) and master cleaning schedules (MCS). Comply with Company, third party and Customer standards demonstrated by successful completion of Inter-lab more »

and on occasions as required If you would like to discuss this further, please contact Mark Bux-Ryan for further information. QP, qualified, person, GMP, manufacturing, sterile, terminally, sterility, aseptic, quality, assurance, manager, leader, MHRA, audit, release more »

and on occasions as required If you would like to discuss this further, please contact Mark Bux-Ryan for further information. QP, qualified, person, GMP, manufacturing, sterile, terminally, sterility, aseptic, quality, assurance, manager, leader, MHRA, audit, release more »

and on occasions as required If you would like to discuss this further, please contact Mark Bux-Ryan for further information. QP, qualified, person, GMP, manufacturing, sterile, terminally, sterility, aseptic, quality, assurance, manager, leader, MHRA, audit, release 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 »

safety and legality can be assured and that all the necessary information is accurately recorded and retained The Position: Carry out Daily/weekly GMP audits as required. To complete a detailed shift ... more »

from a Pensions background and ideally Team Leading people working on similar projects as listed below. - Pensions Data Transfer - Client Onboarding - Implementation - System Configuration - GMP - BIBO - Buy in - Buy out - Pension projects Unique culture, fully diverse and inclusive, very supportive, with ability to grow and become senior manager. Responsibilities: Takes more »

of swabs & water samples Quality checks and then collection of finished product and raw materials for microbiological & nutritional testing Conducting various daily audits (including GMP, Glass & Plastics audits, and ensuring corrective action with the shift manager Conducting internal quality assessment panels (QAS) throughout the shift & raising issues with the senior more »

are seeking a dynamic individual with experience of working in radiopharmacy and/or technical services. Experience of working in Quality Assurance or a GMP-controlled environment is desirable. Please note that the vacancy may close early if a suitable amount of applications are received. Main duties of the job … part of the overall Radiopharmacy Pharmaceutical Quality System. The post-holder will contribute to ensuring that the department complies with the requirements for Good Manufacturing Practice, as defined in The Rules and Guidance for Pharmaceutical Manufacturers and Distributors (Medicines and Healthcare products Regulatory Agency). The post-holder will contribute … units or at least 1 year in Radiopharmacy units. Desirable Experience as releasing officer in MHRA "Specials" Unit Experience in Education and Training within GMP and Radiopharmacy environment Experience in validation of equipment Experience in validation of processes Experience in project management and service development Knowledge Essential Good practical knowledge more »

and improvement of the Quality Management System (QMS). Assure the compliance of all activities with Good Distribution Practice (GDP) and Good Manufacturing practice (GMP) requirements. Responding to medical information enquiries from healthcare professionals, community pharmacies, patients, and wholesalers. Ensuring the completion of checks for new products; having the appropriate more »

repairs 5. Assists in the operation and maintenance of the flow and tracking of devices through the Affiliate. 6. Maintain good departmental housekeeping to GMP/GLP standards and ensure compliance with safety recommendations regarding the use of Personal Protective Equipment (PPE). 7. Identify potential process and documentation improvements more »

time-served Mechanical Engineer in a manufacturing/engineering . Experience ideally gained over a period of 3+ years in FMCG and/or GMP environment Health and Safety knowledge If this position sounds as if it could be of interest, then please apply here and Jamie Lunn from D more »

Supporting seal samples. * Release of components and ingredients to Good Stock. * Ensure all operating areas and equipment are maintained to the required levels of GMP and cleanliness. * Ensure all health and safety and environmental standards are maintained. Key Responsibilities and accountabilities: * Supporting the Quality System and the continual improvement philosophy. more »

including HR duties eg: PDRs Organising the safe and efficient production of aseptically prepared products Delivering full training to production staff taking part in GMP activities, ensuring proficient and safe working within an Aseptic Services Unit Supporting co-ordination of operator validations and competency checks. Co-ordinating workflow and workforce … precision required for aseptic manipulations. Long periods of concentration performing accuracy checks. Responsibility for Patient Care Maintains compliance with Rules and Guidance to Good Manufacturing Practice and any other local, regional and national guidance documents. Assists with the maintaining Quality Assurance Standards in accordance with National, Regional and local requirements. … and reporting any deficiencies. Responsibilities for Human Resources Supervises Band 4 Technicians and Assistants groups within the aseptic suite to ensure compliance with Good Manufacturing Practice and departmental procedures and protocols. Participates in the recruitment process for Band 4 Pharmacy Technicians, Science Manufacturing Technicians and Assistants. Performs appraisals with junior more »

equipment. You can troubleshoot test processes. You can perform periodic equipment inspections and preventative maintenance work. Your Experience: Lab-based experience would be advantageous GMP or GDP experience You will have high attention to detail Able to work both on individual tasks and as part of a wider team IT more »

to help our patients. We value and encourage learning and development. As the Quality Assurance officer you will support the QA Manager in overseeing GMP compliance, contribute to the management of QMS and ensure the maintenance of quality certifications and standards throughout the manufacturing, testing and release of the product. … companies QMS. · Support with assessment of deviation event investigations. · Support closure to plan of Change Controls and CAPA actions. · Issue, review and approval of GMP batch manufacturing records to support certification and release. · Assist in performance of internal self-inspection audits. · Support the Company’s Quality Meetings. · Assist in maintaining … the Company’s quality certifications, e.g. GMP, GDP, HO approvals, etc. · Assist in preparation for inspections from MHRA and other Competent Authorities · Provide quality review and input to manufacturing and business activities. · Ensure compliance with the Company’s Quality Standards. · Engage with the wider team and sector to gain wider more »