76 to 100 of 155 GMP Jobs in the UK

include understanding and applying relevant standards so that Bakkavor, Customer and Legal requirements are achieved and maintained. This role is key to driving improve GMP standards and audit results across the site. You will influence and work collaboratively with the operational teams and agree solutions together. Duties include: <... more »

biopharmaceutical company in the North of the UK. Looking for a CSV Engineer who has experience in: Testing analytical and lab support systems to GMP requirements. Working closely with IT & Laboratory departments to interface lab equipment with company network for secure storage of generated test data and backup of test 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 »

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 »

ConsultancyAuto, Energy and/or FMCG experience preferred Skills & CompetenciesStrong understanding of and competency with Ad/MarTech platforms like:Adobe (AAM and CDP)GMP and GA4Understanding of media effectiveness measurement techniques through advanced analytics (modeling) solutions like:MMMIncrementalityBrand Equity ModelingProficiency in building 1st party data strategies including the associated 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 »

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 Be the Engineering point of contact during & out of hours Respond to more »

criteria outlined in personal specification Disposition, attitude and motivation Essential Demonstrates criteria outlined in personal specification KNOWLEDGE & EXPERIENCE Essential Interest in Science Understanding of GMP Understanding of environmental monitoring techniques Desirable Demonstrable experience in a medical or health related environment or clean room environment. Previous demonstrable aseptic experience Computer literate 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 »

Desirable JAC computer system knowledge Qualifications Essential GCSE grade 4-9 Math and English or equivalent Desirable NVQ2 in Pharmacy Services or evidence meeting GMP standards Other Essential Upholds and models Trust Values Desirable Willing to be flexible to service needs Disclosure and Barring Service Check This post is subject 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 »

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 »

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 ... APCT1_UKTJ 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 »

in investigation and corrective action implementation. * Working as a support function to operations to ensure hygiene levels of the facility are maintained by conducting GMP/Glass and Hard Plastic and Fabrication audits in conjunction with departments leads to assess compliance and improve standards. Report findings as identified within the 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 »

bench to bedside concept.Working under the trusts Pharmaceutical Quality System, the post holder will use their experience and specialist knowledge in Good Manufacturing Practice (GMP), immune cell culture, immune cell purification by high end multicolour flow Cytometry and or other methods to take responsibility for developing and delivering the manufacturing … expansion. Required to work with collaborators in developing processes by taking pre-clinical ideas and technology transferring to the unit and ensuring phase appropriate GMP compliance Lead Validation and qualification procedures for processes and equipments used for manufacture of immune cell products3 Provide specialist knowledge of the latest developments within … implementing independently controlled documents: Investigational Medicinal Product Dossiers, Product Specification Files, Batch Manufacturing Records and Standard Operating Procedures (SOPs) for Production activities in the GMP unit. Ensure adequate maintenance and supervision of equipment, and ensure compliance with Planned Preventive Maintenance (PPM) Undertake strategic judgements based upon specialist knowledge of the 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 »

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 »

to demonstrate the ability to learn the technical aspects of processes. Able to show an understanding and willingness to comply with all food standards (GMP, health & safety etc.) consistent with working in a world class food manufacturing environment. WE SUPPORT AND CARE FOR OUR EMPLOYEES BY PROVIDING YOU WITH We 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 »

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 »