12 GMP Jobs in Scotland

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 »

Following full training, you will work within a small team, ensuring your daily workload is completed on time whilst working within a highly regulated GMP facility. To be considered for this role you must have: BSc/MSc in a Scientific or Engineering subject A natural interest in maintenance or 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 »

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 »

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 »

a cGMP environment Experience of supplier audits and/or vendor assurance would be beneficial Excellent organisational and time management skills Good knowledge of GMP and ISO regulations Awareness of regulatory requirements more »

role would be responsible for supporting the centralised Customer Quality Technical Agreement (QTA) process in accordance with international regulatory, company and GMP standards (Good Manufacturing Practice). You will work within a cross-site organisational team to support the issuance of new Quality Agreements, amendments to Quality Agreements and revision more »

/revised within the documented revision time span Ensure that all documents are updated and mastered according to existing procedures Assist in compliance with GMP regulations Requirements: Educated to HNC/HND as minimum- degree preferred Experience in document review in a regulated (GMP) environment Excellent written and verbal communication more »

Private Healthcare + Free Parking + Life Insurance + Pension + Ongoing Training + Progression Are you a Laboratory Manager with a background in GMP looking to join a company that is passionate about revolutionizing cancer therapy? You will take on a leadership role where you will receive full product … Your duties will encompass supervising production operations, resolving issues in cell culture processes, and spearheading quality investigations. Your meticulous oversight will ensure adherence to GMP standards and facilitate the seamless integration of novel procedures. This role would suit a Laboratory Manager with a background in GMP looking to join a … role where you will receive full product training, tremendous growth opportunities all while working hybrid. The Role: Manage T cell-based therapy production, maintaining GMP compliance. Lead production, troubleshoot processes, and conduct quality investigations. The Person: Life Sciences or related field background. Regulatory knowledge of T cell Therapy. Demonstrated leadership 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 »

shape, develop and manage your own team, drive quality, improve standards and ensure the development and cell trials are on time and adhere to GMP standards. The company has been established since 2014 with ambitious, yet achievable, plans for growth including expansion into the US market and are a company … operations Perform problem/solving trouble shooting of cell culture production Lead quality investigations/deviations Ensure quality standards are maintained in compliance with GMP standards The Person: Life Sciences discipline background T cell Therapy regulatory knowledge Passionate about making a difference within cancer treatment Cell therapy, pharmaceutical, production, t more »

shape, develop and manage your own team, drive quality, improve standards and ensure the development and cell trials are on time and adhere to GMP standards. The company has been established since 2014 with ambitious, yet achievable, plans for growth including expansion into the US market and are a company … operations Perform problem/solving trouble shooting of cell culture production Lead quality investigations/deviations Ensure quality standards are maintained in compliance with GMP standards The Person: Life Sciences discipline background T cell Therapy regulatory knowledge Passionate about making a difference within cancer treatment Cell therapy, pharmaceutical, Laboratory, production more »