26 to 50 of 195 Permanent GMP Jobs

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 »

and vision systems integrated within packaging equipment including interfaces with enterprise systems. Responsible for providing cGMP compliant control systems as per GAMP5 and EU GMP Annex 11. Key Experience Essential - Practical experience working within manufacturing and packaging environments Experience of the automation project lifecycle including design, configuration, implementation, testing, commissioning 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 »

be considered, to be clear we are looking for someone who has commercial lab experience working to QMS like UKAS 17025 or GLP/GMP/BRC) or GC/MS experience Strong interpersonal, organisation skills Able to work towards deadlines Good IT skills Important Information: We endeavour to process 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 »

site and related functions are in 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 ownership for key quality system elements and will support and execute site quality more »

degree level or above in life sciences, chemistry or a related file with experience of working in a regulated laboratory environment (e.g. GLP or GMP) • Experience in using and troubleshooting ELISA analytical systems as well as the ability to develop and validate analytical methods using ELISA. • The ability to document more »

profile and past history: 1. Relevant degree in a chemistry related discipline. 2. Proven industry experience in development activities for drug development in a GMP environment. 3. A working knowledge and practical experience with management of an analytical chemistry function/facility in the pharmaceutical industry. Hyper Recruitment Solutions Ltd more »

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 »

miles from Peterborough and 12 miles from Spalding. About the role. Participate and direct QA team to observe and audit production processes and GMP, ensuring products are made to specification and within customer codes of practice and Bakkavor standards, reporting findings to managers as appropriate Assist in delivery of site more »

URS, DRR/VRA, IOQ, OCD, C&QR, RTM, and VR. Execution and approval of the corresponding protocols to release the required equipment for GMP production Weekly Validation Report Draft, execution, and approval CSV/CQV validation protocols Qualifications & Requirements: Applicants will have experience of general validation on multiple projects 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 »

your professional growth Employee Assistance Program for holistic support KEY RESPONSIBILITIES: Quality Assurance Audit Program: Oversee all internal and external audits (Quality, Food Safety, GMP, Ethical Certifications, Customer) Create and manage the site audit calendar Support internal audits per BRC requirements Log and address non-conformances Collaborate to resolve audit more »

methodologies, 21 CFR Part 11, and GAMP. Develop detailed specifications, engineering documents, SOPs, and operating standards. Oversee and manage process control automation in a GMP-regulated manufacturing environment. Handle process change control requests according to established SOPs and processes. Lead technical root cause analysis, incident investigations, and troubleshooting for process 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 »

+ 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 »

Quality Assurance analyses/functions in the processing of raw materials to finished goods and ensure compliance to company, customer, FDA, DOC, USDA and GMP specifications and regulations. Perform the Quality Assurance functions of production lines and/or the Quality Assurance bench product analysis for the lines and tankers more »

site & escalate/action where necessary 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 Carrying out sampling and swabbing & leading on investigations corrections -preventative procedures To be the subject matter expert more »

site & escalate/action where necessary 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 Carrying out sampling and swabbing & leading on investigations corrections -preventative procedures To be the subject matter expert more »