1 to 18 of 18 Permanent GMP Jobs in the UK excluding London

The role is required to ensure GxP compliance is maintained through supporting the operational teams in the delivery of IFM services (e.g. technical maintenance, GMP cleaning & supplier management) This is a critical role which provides wide exposure to both us and Client management, provides a unique opportunity to learn the more »

Head of QA and RA, Responsible Persons and Qualified Persons with the implementation and maintenance of the Quality Management System in accordance with the GMP and GDP guidelines and GPhC, ISO 9001 and ISO 13485 standards. Ensuring ongoing compliance with relevant standards, legal requirements, regulations and the PSDL documented policies more »

testing and manage the calibration system Support the Technical Manager and deputise in their absence, ensuring smooth departmental operations Conduct regular site audits, including GMP, glass, and hard plastic audits, and drive improvements with operational teams Ensure all technical documentation is audit-ready at all times Person Specification A degree more »

activity in ensuring compliance with the site FSQMS, any necessary audit standards and legal requirements Support factory compliance with FSQMS including managing and organising GMP and fabrication audits Support factory compliance with traceability requirements including leading traceability exercises and organising for tests of the system Manage and help maintain documents more »

of theQuality Assurance Officer(QA Officer) Experience working in a QA role in Pharmaceutical,Food, FMCG Knowledge of all relevant practices associated with site GMP, Knowledge of processing, production and packing methods for products Good communication skills to ensure information is taken, used and given at all levels for maximum 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 »

Carry out site audits as part of the internal audit programme and follow up with teams with improvement actions plans in place ·Carry out GMP, hygiene, housekeeping and fabrication audits and identify areas of improvement ·Carry out non-conformance investigations and assisting in resolutions ·Liaise with cross-functional teams (production more »

meals and modern deli products for a dedicated customer. 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 more »

validation, customer audits/quality requests, and material and product disposition. The QA officer is expected to identify, escalate and work to address any GMP/GxP issues with potential impact to product quality or quality compliance. Together we offer fantastic opportunities for committed employees to learn and develop their … of products. Where potential issues exist, these are to be highlighted to the QA manager. Promote and work to ensure compliance with all relevant GMP/GxP requirements. Support and lead as required, quality process improvements and quality management system improvements within the department and on site. Escalate any identified … GMP/GxP areas of concern to Quality Management and QP.Warehouse on call team. more »

business based in North West of England. This is an excellent opportunity to join a well-established and growing organisation. The role will support GMP product manufacture so a degree of flexibility to working is required. Purpose of the Role of QA Compliance Officer Support, input and develop the Quality … working in a QA compliance role in Pharmaceutical or Medical devices or Food or FMCG Knowledge of all relevant practices and compliance associated with GMP or HACCP. Knowledge of delivering QA and compliance to processing, production and packing methods for products Good communication skills to ensure information is taken, used more »

searching for a Lead Qualified Person (QP) to join a leading Pharmaceutical manufacturer in Northern England. As the Lead Qualified Person, you will ensure GMP compliance for the site and focus on the release of small molecule batches. Your responsibilities as the Qualified Person will be: The batch certification and … on manufacturing floor GEMBA walks. To provide support, guidance and advice on Quality matters to all departments within the company, contributing to the company GMP strategy. The successful candidate for the Qualified Person position will demonstrate the following: Extensive experience in Quality Assurance roles within the Pharmaceutical industry, with on … agile and flexible to enable them to adapt to situations when required. Quality Assurance | QA | QP | Qualified Person | Deviations | OOS | OOT | GEMBA | GMP | Good Manufacturing Practice | Orange Guide | Small molecule more »

naturally a flexible mindset is needed for this type of position. As such, I am interested in speaking with people from Production and QC GMP settings, as well as fresh graduates looking to get that key break. This team is very open to your background – it is all about your … experience would be advantageous but is not essential Experience and/or understanding of chromatography techniques including HPLC and GC. A solid understanding of GMP principles – or at least the ability to work to strict regulated procedures Flexible to work shifts Must have own transport to access the site due … to shift work QC, quality, control, analyst, analytical, laboratory, radiopharmaceutical, GMP, entry, graduate, science, pharmaceutical, biotechnology, manufacturing, shift more »

for implementing and maintaining quality standards in line with regulatory requirements and company policies. The role involves overseeing quality-related activities, ensuring compliance with GMP, conducting audits, managing documentation, and contributing to continuous improvement processes. Key Responsibilities: You will: Support daily operations of the Quality Assurance department. Adhere to GMP. … in writing. Demonstrates proficiency in Microsoft Word, Excel, and PowerPoint. Demonstrate attention to detail. Ability to work independently and collaboratively. Comprehensive awareness of EU GMP regulations, directives, and guidance. Desirable Experience working within the Pharmaceutical Manufacturing Industry Experience in use of eQMS systems What you'll get in return Flexible more »

seamless transitions from NPI to production. You’ll lead initiatives to drive continuous improvement. Process Validation: Ensure all processes comply with Good Manufacturing Practice (GMP) and adhere to all quality system documentation standards. Documentation and Compliance: Maintain detailed manufacturing documentation and technical reports, ensuring all work aligns with company quality 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 »

Operational Technology Engineer Role: Operational Technology Engineer or Manufacturing Systems Engineer Specialisms: Operational Technology (OT), Manufacturing Systems, GMP (Good Manufacturing Practice), GPO, IT Security, IT Engineering, Manufacturing, Pharmaceuticals Type: Contract Location: Stevenage Work Pattern: On-Site (shift based) Duration: Rolling Contract (Long-Term) Start: ASAP/Urgent Pay Rate … and working varying shifts (6am – 10pm)* Role Requirements • IT Communication & OT tablet/PC builds • Network patching • Remote access provisioning • Port audits and patching • GMP Change management and document updates • GPO recommendations and deployment • Managing OT PC image and IT communication tablet image with version control • Troubleshoot issues between physical … BAU initiatives Required Skills & Experience • Demonstrable experience in Operational Technology and/or Manufacturing technical support • Core understanding of Operational Technology principles • Appreciation of GMP regulations and how this impacts day-to-day working practices • Understanding of data/meta-data/raw data/data integrity • Appreciation of application 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 »

Job summary You will be joining NHSBT at a particularly exciting time as we embark on a journey of change, enhancing our current IT service provision. You will lead the systems testing required to ensure the NHS Organ Donor Register more »