1 to 25 of 31 Permanent GMP Jobs in the North of England

Ensures that there are robust processes in place for the review and release product for GLP and GCP studies. Ensures appropriate quality oversight of GMP activities performed by the Product Development teams at Dechra or CDMOs and contract laboratories. This may include review and approval of protocols, reports, methods, master more »

have requirements: 2-5 years’ experience working with MES/EBR or similar systems in the life sciences industries. Experience deploying MES in a GMP environment, configuring Recipes, MBR’s, Materials, BOMs, Order Management, Equipment management, Batch Review/Approval and other typical components. A background in one or more more »

PhD or relevant degree in any chemistry or life science related subject. The ideal candidate will have previous experience of working to GLP/GMP Must be IT literate with competent use of the Microsoft systems. The ideal candidate will have previous experience of using LC-MS/MS. Previous more »

with all company policies and procedures. Employee works in accordance with the installed ISO 9001 quality system and, if applicable, works in accordance with GMP-API. Your Profile BSc with previous working experience in a peptide lab is essential, MSc preferred Previous experience in a similar role would be desirable 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 »

+ 8 Bank Holiday Cycle to Work Scheme Skills and Qualifications Required for Analyst BSc or higher in Chemistry or related field Experience within GMP environment Physical characterisation including; particle sizing (image and laser diffraction), specific surface area, XRD, thermal analysis, water content Chemical ID analysis including; UV-vis, FTIR 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 »

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 »

Middlesbrough area. Salary and Benefits of QC Analyst Salary up to £27,000 Permanent Role Skills and Qualifications needed for QC Analyst Awareness of GMP/GLP Standards Pharmaceutical or Chemistry Degree 2 Years Experience in a relevant role Fine Chemistry/Pharmaceutical Experience 2 years of HPLC and GC more »

Middlesbrough area. Salary and Benefits of QC Analyst Salary up to £27,000 Permanent Role Skills and Qualifications needed for QC Analyst Awareness of GMP/GLP Standards Pharmaceutical or Chemistry Degree 2 Years Experience in a relevant role Fine Chemistry/Pharmaceutical Experience 2 years of HPLC and GC more »

correctly. Ensure that the aseptic process is carried out in compliance with current Standard Operating Procedures following the principles of the Good Manufacturing Practice (GMP). About us Liverpool University Hospitals NHS Foundation Trust was created on 1 October 2019 following the merger of two adult acute Trusts, Aintree University … correctly. Ensure that the aseptic process is carried out in compliance with current Standard Operating Procedures following the principles of the Good Manufacturing Practice (GMP). See Job Description for further information. Person Specification Experience Desirable Experience working in Healthcare Environment Experience of stock rotation Experience of working in stores more »

all levels - work under own initiative 2+ Years QA experience within Food Manufacturing, ideally with both private label and branded product experience. Proficient in GMP and Quality Standards. Level 3 HACCP Level 3 Food Safety Auditor qualification Recognised allergen qualification Recognised microbiology qualification Working hours: 18:00/ 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 »

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 »

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 »

all maintenance activities across the drifferent shifts * Ensure all work is carried out and documented to the highest standards to meet Lonza GMP (Good Manufacturing Practice) requirements * Solve technical problem following RCA (Root Cause Analysis) techniques * Ensure all engineering work is carried out to Lonza EHS, standards * Take an ownership … and the equipment the department maintains Requirements: * Willingness to participate in a shift rota including Nights and Weekends * Experience in working to GMP (Good Manufacturing Practice) standards is preferable but not essential * Calibration and instrumentation experience * Understanding of mechanical production equipment i.e. pumps, centrifuges,line running, pressure-reducing sets etc 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 »

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 »

clinical trials and practice research. Experience of supervision of staff. Experience in delivering training and education to staff. Understanding of the principles of Good Manufacturing Practice and Quality Assurance Understanding of Section 10 exemption of the Medicines Act and the requirements that this brings Understanding of Good Clinical Practice and … Band 8a - Sound understanding of the principles of Oncology/haematology Band 8a - Evidence of delivering service improvements. Band 8a - Working knowledge of current GMP and QAAPS standards and legislation. Band 8a - Enhanced knowledge of Good Clinical Practice and experience of handling clinical trial material (IMP) in an aseptic unit. more »

naturally a flexible mindset is needed for this type of position. As such, I am interested in speaking with people from Production and QC GMP settings, as well as fresh graduates looking to get that key break. This team is very open to your background – it is all about your … experience would be advantageous but is not essential Experience and/or understanding of chromatography techniques including HPLC and GC. A solid understanding of GMP principles – or at least the ability to work to strict regulated procedures Flexible to work shifts Must have own transport to access the site due … to shift work QC, quality, control, analyst, analytical, laboratory, radiopharmaceutical, GMP, entry, graduate, science, pharmaceutical, biotechnology, manufacturing, shift 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 »

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 »

global pharmaceutical company who require a QA Production Support Supervisor/RP to join their well-established Quality and Operations team, focusing on the GMP and GDP requirements. This role involves the supervision and mentoring of a team of very capable Quality Assurance Production Support Officers. Responsibilities: Qualified RP/… systems (including, but not limited to the complaints and batch release processes) Write, implement, review and maintain SOPs, policies and other documentation for QA GMP and GDP activities. Act as Quality GMP and GDP advisor on site projects such as new product introductions or CAPEX projects. Host training sessions on … GMP and GDP QA related topics. Requirements Extensive GMP Quality Assurance experience, preferably in production support Experience of line management and leadership Qualified RP/RPi SRG is UK’s number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices more »

ABOUT YOU Are you a Quality professional with experience in a GMP laboratory, looking for a role that will challenge you, and help you develop new skills? You will possess rigorous attention to detail and be hungry for a challenge out of the lab. We need you to have: BSc …/MSc/PhD in Chemistry (or related scientific discipline) A sound working knowledge of relevant quality standards; GMP, GLP, GCP and other analytical related quality standards Good working knowledge of Quality Assurance in the Chemical and Pharmaceutical Industry Quality Assurance background which includes some specialist knowledge within a defined … Excellent attention to detail Impressive written and verbal communication ABOUT THE OPPORTUNITY You will provide general support to Quality Assurance activities relating to GLP, GMP, GCP, and other similar Quality Systems established to ensure that the appropriate standards and effective working systems and relationships are maintained and where necessary improved. 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 »