26 to 50 of 157 GMP Jobs in the UK

other DSP, Facebook, Twitter Experience of managing vendor relationships Regularly contributes to platform best practices and campaign processes Experience with Google stack and have GMP & Adwords certifications (desirable) Experience with running campaigns across multiple countries/languages Experience with managing a mid- to large-sized team across a range of more »

the wider Quality group at Alba Bioscience, part of AliveDx, and its primary role is to ensure that all aspects of Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) compliance are met through effective control of the Quality Management System (QMS). The role is a full-time temporary … by the business . Participate in an 'in-house' programme of continuous training and assessment. Conduct all duties in compliance with Good Manufacturing Practice (GMP), Good Documentation Practice (GDP) and appropriate regulatory requirements including statutory Health & Safety legislation and internal practice. Perform any other duties as reasonably requested from the more »

computer programs to analyse project results Micro biological training Understanding of technology relevant to business area and area of responsibility Understanding of technical KPIs GMP knowledge of techniquesIf this sounds like you join us, grow with Greencore and be a part of driving our future success. What you'll get more »

be key. You will be energetic, punctual, proactive, and reliable with the ability to lead, guide, and motivate others towards achievement whilst maintaining good GMP Standards. What you can expect from us: When joining us you can expect a highly competitive rewards package including group pension and other flexible benefits more »

satisfy the requirements of external agencies. Responsible for timely and accurate reporting of internal Refresco KPIs to the management team. Be responsible for ensuring GMP and Hygiene standards are communicated to the operational teams and processes are in place to effectively monitor and manage them. Partake in site visits and more »

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 »

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 »

at a high level. What are we looking for? Essential Degree Qualified in an area related to an Engineering discipline. Experience gained within a GMP environment (or closely related regulatory environment) from an equipment, facilities, and engineering perspective. Demonstrated working knowledge of BMS, EMS & HVAC systems. Strong interpersonal and communication more »

a BA - circa 5+ years to work independently. Experience with Veeva and other quality systems. Must understand GXP. Order of focus - GCP, GDP/GMP and then GLP. Extensive experience and knowledge in Quality Assurance in Pharma/biotech space to interact with stakeholders. Not a validation specialist but understands more »

site and related functions in maintaining compliance with GxP regulations and applicable quality guidelines, including, but not limited to UK/EU/US GMP/GDP, ICH and other region specific guidance. The individual will have support key quality system elements and compliance improvements, working closely with relevant stakeholders more »

time. Main responsibilities: Use a range of analytical chemistry techniques- predominantly HPLC Ensuring all analysis and documentation are conducted and recorded in compliance with GMP standards Perform stability study programme activities, storage of in process, and final products samples and retention sample management Working to set protocols within a busy 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 »

service, we will do our best to make it work for you. Person Specification KNOWLEDGE Essential Up to date knowledge and understanding of GCP,GMP and its application Evidence of preparing worksheets/procedures Knowledge and understanding of the Law and Ethics relating to the dispensing of medicines. Working knowledge 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 »