51 to 75 of 90 Permanent GMP Jobs in the UK

skills in previous positions. Worked as an engineer or come from an analytical background carrying out on site support. Experience working in GLP/GMP environment. Be prepared to travel and stay away as required. Package: Salary up to £43,000 D.O.E Bonus Scheme (£6.5k) Company Car + Expenses Covered more »

this time. About The Role Working as a Multi-Skilled Engineer, preferably with an electrical bias you will primarily offer engineering support in the GMP area. You will also handle responsibilities related to site utilities and facilities as needed. Your duties will include completing both scheduled and unscheduled maintenance tasks more »

Job you will do: Ensuring the maintenance of all external certifications including ISO 9001, ISO 45001, ISO 14001, ISO 50001, IATF 16949, AS 9100D & GMP Ability to host and support 2nd and 3rd party audits/inspections over all management systems. Supporting departmental managers in the creation and maintenance of more »

in Electrical Engineering Solid practical electrical/mechanical hands-on experience maintaining machinery, able to work on own initiative. Experience of working in a GMP environment. A strong communicator, working closely with engineering and production teams. Experience working on conveyors, sensors, automation, etc. Experience within FMCG in a process or more »

desirable (comprehensive training will be given). Close attention to detail to produce work of a high standard is essential and documentation completion to GMP standards. A systematic and logical approach to problem solving & ensuring a high level of customer service is delivered. Package: Salary Dependent on Experience! 7% Performance more »

co-ordinate the day to day workload, ensuring items are manufactured in a timely manner and colleagues are supported. To follow good manufacturing practice (GMP) at all times. To generate worksheets and labels, ensuring medicines are charged correctly using the pharmacy computer system. To in process check worksheets and labels more »

services and ensure that all products are appropriately, efficiently and cost effectively prepared within the unit, according to the Guide to Good Manufacturing Practice (GMP) and that pharmaceutical guidelines relevant to aseptic dispensing (production) and departmental procedures are followed To provide pharmaceutical advice to patients/carers/ward staff … training in Technical Services Registered with the GPhC or relevant professional body Up to date CPD portfolio Knowledge: Essential Understanding of the principles of GMP and QA in Aseptics/Production manufacturing environment Understanding of Pharmaceutical Quality Systems Knowledge of Audit and validation Computer and IT competent COSHH Regulations and … Cato aseptic workflow system Experience: Essential Post qualification experience (at least 2 of which have been in hospital preparative services)Working in a Pharmaceutical GMP manufacturing facility or in a manufacturing environment that employs a quality system (Previous Production/Aseptic experience). Demonstrate ability to deliver induction and competency more »

Note: Applicants must be authorised to work in the UK Our client is a leading pharmaceutical distributor with multiple GDP distribution facilities and a GMP assembly unit. They are committed to maintaining the highest standards of Good Manufacturing and Distribution Practice (GDP) and regulatory compliance. Their dedication to quality, safety … to move forward with your application. Other suitable skills and experience include Responsible Person (RP), Quality Affairs Specialist, Compliance Manager, Pharmaceutical Quality Control Manager, GMP Auditor, Distribution Manager, Pharmaceutical Consultant, Quality Systems Coordinator. more »

qualified), with practical QP experience in a UK pharmaceutical setting, certifying product to market Knowledge of relevant EU legislation, particularly around good manufacturing practice (GMP), with experience working in a fast-paced, high volume environment Certifying multiple dosage forms would be beneficial, but solid dose and steriles experience would be more »

of pharmacist as required3.Participation in screening, dispensing and checking of clinical trial prescriptions, and advising others of Good Clinical Practice (GCP), Good Manufacturing Practice (GMP) and requirements relating to Investigational Medicinal Product (IMP) management.4.To participate in the Trust-wide Out of Hours Medicines Advice Service and seven-day medicine supply more »

Oversee multiple QA projects, ensuring timely and effective execution. Compliance and Quality Assurance: Ensure all operations comply with regulatory standards (MHRA, FDA, etc.) and GMP guidelines. Risk Management: Identify and mitigate risks associated with aseptic processing. Continuous Improvement: Drive initiatives to enhance product quality and operational efficiency. Requirements: Experience: Minimum … and developing a team. Project Management: Strong project management skills, with the ability to handle multiple projects simultaneously. Technical Knowledge: In-depth understanding of GMP, aseptic processing, and regulatory requirements. Communication: Excellent interpersonal and communication skills, with the ability to influence and collaborate across all levels of the organization. Problem more »

searching for a Lead Qualified Person (QP) to join a leading Pharmaceutical manufacturer in Northern England. As the Lead Qualified Person, you will ensure GMP compliance for the site and focus on the release of small molecule batches. Your responsibilities as the Qualified Person will be: The batch certification and … on manufacturing floor GEMBA walks. To provide support, guidance and advice on Quality matters to all departments within the company, contributing to the company GMP strategy. The successful candidate for the Qualified Person position will demonstrate the following: Extensive experience in Quality Assurance roles within the Pharmaceutical industry, with on … agile and flexible to enable them to adapt to situations when required. Quality Assurance | QA | QP | Qualified Person | Deviations | OOS | OOT | GEMBA | GMP | Good Manufacturing Practice | Orange Guide | Small molecule more »

s products. Provide US and European regulatory intelligence, train Subject Matter Experts and provide internal consultancy for quality compliance implementation and FDA/EU GMP/GDP remediation projects in the Dechra Internal Manufacturing network. Frequent global travel is required with this role. Main Responsibilities So, what will you be … manufacturing network (as required) across the product's registered lifecycle in compliance with all applicable ISO, ICH, FDA, EU, and national regulatory requirements for GMP/GDP. Lead GMP/GDP audits for Dechra DPMS based on specific expertise, criticality, and complexity. Periodically assess the liability, regulatory and/or … networks are all being adequately monitored. Recruit, lead, train and develop, as required, the team of quality and compliance experts (specialised in auditing different GMP/GDP areas) across the business, to keep the business abreast of ongoing developments through benchmarking activities, whilst proactively identifying and addressing any gaps relating more »

options. Reporting to: CEO Our client is an innovative biotechnology company based outside of the centre of Cambridge. They specialise in the synthesis of GMP grade gene constructs utilising an enzymatic synthesis. Their technology provides exciting possibilities for ensuring cheaper, faster and more accurate DNA/gene constructs than traditional … transfer activities. As a Director of Manufacturing, you will be responsible for: Continuing the expansion and development of manufacturing processes and frameworks across the GMP cleanroom facilities for DNA production. Supporting technology transfer projects from the research and development teams. This will include the review and submission of SOPs. Spearhead … audits, regulatory submissions etc. Build and oversee cross-departmental relationships with R&D, quality, regulatory teams etc. Lead the daily organisational activities of the GMP team and take responsibility for staff training. Act as a point of contact for external clients with respect to project updates and regulatory plans. Manage more »

company dedicated to improving health and wellness through cutting-edge products. Committed to excellence, they operate to the highest standards of Good Manufacturing Practices (GMP). Key Responsibilities: Oversee and maintain the Quality Management System (QMS) to ensure compliance with GMP standards. Conduct thorough internal audits and participate in external … reviews to identify areas for improvement and ensure continuous quality enhancement. Collaborate with cross-functional teams to implement quality processes and provide training on GMP compliance. Develop and update quality policies, procedures, and documentation to align with industry best practices. Requirements: Bachelor's degree in a relevant field (e.g., Life … Sciences, Pharmacy, Quality Management). Proven experience in quality systems management within the Medical Nutrition or Pharmaceutical industries. In-depth knowledge of GMP standards and regulatory requirements. Strong analytical skills with a keen eye for detail. Excellent communication and interpersonal abilities to work effectively with various teams. Experience in leading more »

be responsible for supporting the Quality Management System (QMS) and verifying the adherence of manufactured products for human use, in line with current Good Manufacturing Practice (cGMP). As part of a busy team within a rapidly growing organisation, operating within a challenging industry you will benefit from the numerous … To be successful in this role, were looking for you to have: A-level qualifications (or equivalent Worked within an established Quality System (e.g. GMP, ISO) Writing and producing scientific reports The following criteria would also be beneficial to your application, but is not essential: Bachelors degree (or equivalent) in more »

also oversee the work of junior QC staff, assist in managing the QC laboratory, and participate in assay transfer activities. This role requires maintaining GMP compliance in the QC laboratory. Key Responsibilities Establish, revise, and maintain procedures for QC testing. Maintain QC systems related to in-process, final drug product … and review of reports. Requirements A BA or BS in Chemistry/Biochemistry/Microbiology or other related science. Experience in a GLP/GMP environment. Computer literacy (including MS Word and Excel). Ability to work well with others. Effective communication skills. Good organizational skills. If you are having more »

Essex NHS Foundation. You will be based at Colchester Hospital, however you will be required to work across at Ipswich Hospital. You will have GMP experience within a pharmaceutical manufacturing facility. You will be a team player, joining an established department with a multi-disciplinary team. Our team have various … on raw materials and manufactured products, and maintaining Quality Assurance functions within Pharmacy Technical Services in line with Standard Operating Procedures and current Good Manufacturing Practice (cGMP) requirements. You will be expected to support the Pharmacy Quality Assurance team in ensuring that the regulatory requirements and standards set by the … full details of the responsibilities and duties of this role please see the attached job description. Person Specification Experience Essential Previous experience of pharmaceutical GMP in NHS manufacturing unit or pharmaceutical industry as required by MHRA guidance for specials manufactures for batch release Demonstrated experience of multi- disciplinary working Handling more »

compensated at an enhanced overtime rate) Experience in some or all of the following areas is highly desirable: ISO 9001 Quality systems Working under GMP conditions Maintaining and certifying equipment to British, European, or International Standards (BS EN 12469, ISO 14644, HTM03-01, GMP) PLC-based control systems IIE 18th more »

by performing physical and analytical testing and report accurate results. Duties to include: Being responsible for physical analytical testing. Follow internal methodologies. Adherence to GMP requirements. Accurately record microbiological results within data packages, as received. Execution of protocols. Ensure laboratory housekeeping standards are maintained and documented accurately. Ensure all equipment … detail, able to prioritise workload, positive and flexible approach. One to two years' experience in a similar role would be ideal, but not necessary. GMP experience would be desirable. CVs in Word please. New Appointments Group, Expertly Matching Employers and Jobseekers since 1975. Committed to diversity, equality and opportunity for more »

a Quality Director to head up a Quality department. The Quality Director will promote and integrate quality into every aspect of the business ensuring GMP compliance and meeting the authority's expectation. The role holder will perform all duties required of a Quality Director, provide leadership to the Quality Teams … the business and provide support to sister company for regulatory inspections and conduct self-inspection program Oversee the Pharmaceutical Management System. Implement the current GMP regulations and industry best practices, where applicable Support and develop the QA team Support/lead manufacturing deviation or testing out-of-specification/out … of-trend investigations Audit the contract manufacturing organisation and laboratory against EU GMP and relevant regulations and guideline Qualifications and Skills: Qualified Person (QP) Knowledge and experience in manufacturing and testing of oral dosage forms and topical products Experience in releasing medicinal products in a fast-paced environment Experience in more »

company or CRO Experience on CMC documentation for respiratory devices is important Experience in Drug product development from early to late stage inclusive of GMP/clinical supply manufacture Experience with regulatory documentation for CMC activities on drug substance, drug product both towards FDA and EMA is mandatory Solid experience … with working in a regulated environment under GxP and with adherence to Company SOPs, policies and guidelines Updated knowledge of ICH GMP is required Excellent communication, presentation, and interpersonal skills. Self-driven and motivated team player Familiar with working in a virtual set-up Fluent in written and spoken English more »

Lab Analyst/Senior Lab Analyst Serving Society through Science, Tata Chemicals Europe (TCE) is one of Europes leading producers of sodium carbonate, salt and sodium bicarbonate and other products, from our plants in Cheshire, UK. British Salt has been more »

related to the instruments You will produce timely and detailed reports for equipment Follow the companys procedures and policies as well as ISO and GMP standards on customer sites You will work closely with the technical team such as Field Application Specialist, Technical Sales Specialist, Technical Support Engineer and Sales … in a regulated environment, however training will be provided You may have field service experience working in the pharmaceutical, biological, or chemical industry following GMP or ISO standards in a similar role though candidates from other industries will also be considered (manufacturing, electronics etc.) Ability to work autonomously and unsupervised more »

related to the instruments You will produce timely and detailed reports for equipment Follow the companys procedures and policies as well as ISO and GMP standards on customer sites You will work closely with the technical team such as Field Application Specialist, Technical Sales Specialist, Technical Support Engineer and Sales … in a regulated environment, however training will be provided You may have field service experience working in the pharmaceutical, biological, or chemical industry following GMP or ISO standards in a similar role though candidates from other industries will also be considered (manufacturing, electronics etc.) Ability to work autonomously and unsupervised more »