1 to 10 of 10 GMP Jobs in Scotland

as developing action plans to drive improvement. Your main accountabilities will include: 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 more »

and relevant experience within a food/drink or pharmaceutical industry, including experience working within a quality function. A thorough knowledge of FDA, MHRA, GMP requirements, auditing and legislation is desirable. Other essential behaviours are the ability to work independently, good communication, facilitation skills and attention to detail. This is more »

ready state. Who you are: - Ideally degree qualified in life science or equivalent qualification, you will have worked in a similar position within a GMP or other highly regulated environment. - You will possess effective numeracy and literacy skills and be well versed in ensuring accurate work is always maintained. - Previous 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 »

and validation testing activities. QC Analyst Requirements: Substantial experience in chromatographic (HPLC and/or C), spectroscopic and classical techniques Confident and knowledgeable of GMP and Data Integrity requirements in QC environments Skilled in troubleshooting Pharmaceutical, laboratory or related environment industry experience If you are interested in the above QC more »

safety compliance. Lead and investigate safety incidents to ensure compliance with standards and close out actions. Oversee and manage process control automation in a GMP-regulated manufacturing environment. Lead WAH activities and projects to improve WAH tasks, and support high-pressure washing activities. Ensure compliance with packaging, transport of dangerous more »

operating procedures currently in use, and verifying that study documentation meets the requirements for compliance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) standards. You will manage your workload to ensure that tasks are adequately resourced and scheduled efficiently and effectively, with all work audited and carried out … in line with GLP and GMP principles. You will provide compliance advice and guidance to staff when needed and support Study Directors in resolving issues and discussing projects with clients. Additionally, you will engage with clients regarding any deviations, investigations, or out-of-specification events to ensure that any resulting more »

proactive and timely manner which includes Quality Control testing and reporting of raw materials, in process, bulk drug substance, final products andstability products to GMP and in accordance with Annex 11 Computerised Systems and 21CFRpart11 Good Documentation Practices for Electronic Data. Perform stability study programme activities, storage of in process … timely manner of any failure of calibration Maintain Quality Control information systems Maintain a technical ability, knowledge and understanding of relevant regulatory requirements for GMP, safety and environmental policies required in order to perform role as QC Analyst Assist in investigation of quality incidents and other problem solving forums and … and conferences where appropriate Carry out general maintenance and house keeping of equipment and laboratories Essential Experience Experience within a QC laboratory working to GMP within a recognised quality system. Ability to organise work within a busy laboratory with experience of writing and working to SOP documentation. Knowledge of GMP more »

laboratory tasks and data analysis promptly and to an exceptional standard, adhering to all relevant procedures, Study Plans, and SOPs. - Comply with GLP/GMP standards, ensuring all activities meet health and safety guidelines and understanding all risk assessments related to the tasks (COSHH, GMO, etc.). - Maintain GMP compliance more »

the Technicians area of responsibility (e.g., a request for some dispensed material). Maintaining the cleanliness and housekeeping within the operations adhering to the GMP standard within the facility — the Process Support Operators are responsible for this being maintained (with the support of Technical, Engineering and Quality staff as appropriate … at any scale, subject to the prerequisite training and safety inductions. Essential Skills and Experience Experience working in a similar operational position within a GMP or other highly regulated environment You will possess effective numeracy and literacy skills and be well versed in ensuring accurate work is maintained at all more »