26 to 50 of 145 GMP Jobs in England

to detail and flexibility. Strong communication skills. Ability to handle stressful situations and controversial issues. Willingness to learn and develop new skills. Knowledge of GMP, GDPR, LSAS, and ethical trade issues. Key Tasks: Prepare and submit regulatory documentation for market registration. Support root cause identification and solution resolution. Conduct and more »

maintained and up to date. Education and experience : *Degree in chemistry, analytical chemistry or equivalent *Previous experience of HPLC, GC analysis with pharmaceutical/GMP regulated environment *Previous experience in analytical method transfer, cleaning validation *your previous experience could be QC analyst, stability analyst, development analyst, principal analyst and raw more »

in Chemistry/Biochemistry/other related science or equivalent experience in a similar setup. - Competent analytical skills, attention to detail, and understanding of GMP requirements. - Ability to work independently and in a team, with strong computer literacy and communication skills. - 1 year of lab based experience is necessary. Are 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 »

+ 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 »

Job summary This position presents an exciting opportunity for an experienced radiochemist or radiopharmacist proficient in PET radiopharmaceutical production to GMP standards. As the Production Manager, you will lead our team of radiochemists at the Positron Emitting Radiopharmaceutical Laboratory (PERL), located within St Thomas Hospital. The ideal candidate must possess … expert knowledge in relevant regulatory governance areas, particularly Good Manufacturing Practice (GMP), as well as Health and Safety, Environmental Safety, and Radiation Protection Regulations (IRR2017 and IR(ME)R). This expertise will ensure adherence to these regulations within the PERL facility. Main duties of the job The role entails … managing radiochemists within PERL to ensure timely, safe, and efficient completion of production duties. Emphasis will be placed on compliance with GMP regulations, development of new procedures and radio tracers, and streamlining processes while maintaining safety standards. This includes supporting the installation and validation of new production equipment. The successful 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 »

least 3 years industrial experience and be able to work on a number of product development projects. Previous industrial experience within a regulated environment GMP environment, pharmaceuticals, food, electronics . Demonstrate project control, with evidence on how you achieved the business goal. Provide support to design operatives to aid in 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 »

in place to meet legal and statutory requirements. Keep records and provide reports in accordance with good engineering practices to external audit standards. Upholding GMP engineering standards across site, statutory inspections are compliant, and any non-conformances are closed out with root cause analysis to avoid repeat failure. Lead the more »

part of the process. * Engage regularly with multi disciplined teams/training and mentoring. * Worked within an Automotive/Pharmaceutical/Medical device/GMP environment. * Bachelors degree or equivalent in Engineering. * DMAIC (desirable). * Lean/Six Sigma qualifications. Travel requirements; Travel between local manufacturing sites is required – no more »

patients, healthcare professionals and other agencies relating to pharmaceutical aspects of clinical trials. To understand EU and UK Clinical Trial legislation relating to GCP, GMP and medicines management and ensure incorporation into the implementation of new clinical trials. To deliver specialist education and training in Clinical Trials to other healthcare more »

for scaling up and down of bioprocess operations. - Understanding of how to develop and optimise processes for the purification of biopharmaceutical products. - Understanding of GMP and QbD considerations in a large scale manufacturing environment. - Understanding and experience with statistical and modelling software and tools. - Understanding of in-process assays such more »

engineering or similar. Substantial demonstrable experience leading a company through ISO9001/13485 relating to medical device instrumentation development and manufacture. Further exposure to GMP manufacture for biological products would be desirable. Comprehensive experience with "quality management" within a technology company including instilling a quality-focused culture and maintainable approach more »

team members on best practices and ensure compliance with regulatory standards. Conduct gap analysis, review change controls, and develop revalidation strategies as needed. Ensure GMP, Data Integrity, and GDP compliance, including timely training. Key Competencies: Proven track record in delivering regulatory-compliant validation strategies. Strong understanding of GxP compliance requirements. more »

as part of the remuneration. Experience: Experienced project engineer or project manager in a pharmaceutical setting A strong understanding and hands on experience of GMP Engineering or validation experience is essential Exposure to the full validation lifecycle and the ability to walk through the full CQV phase Hands on experience more »

safety guidelines and protocols. Continuous Improvement: Driving factory process improvements through techniques like root cause analysis and downtime analysis. Contributing to plant housekeeping and GMP audits and managing logistics team standard tasks. Measures of Success: Clear logistics strategy and plans. Adherence to logistics budget. Decrease in logistic complaints. On-time 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 »

The site Head of Quality will lead the designated site in terms of GMDP quality and compliance, including in the areas of: QA, QC, GMP, GDP, QP activities and RP activities in line with the business goals and plan. Responsibilities: Establish clear and compliant GMDP standards for all site activities more »

and supply chain as well as external partners like CDMOs to achieve objectives and ensure adequate product availability for launch. Ensure compliance with regulatory & GMP/GDP requirements for generic & specialty drug launches in relevant markets. Establish key performance indicators (KPIs) to track launch performance and evaluate post launch success 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 »

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 »

retrieve information from the Council’s various computer systems. Knowledge of current LGPS issues and legislation including but not limited to the McCloud judgement, GMP Rectification, reporting requirements and dispute resolution procedures Minorities, women, LGBTQ+ candidates, and individuals with disabilities are encouraged to apply. Interviews will commence next week, so more »