1 to 25 of 40 GMP Jobs in the UK

validation computer systems - very desirable. Quality experience in a pharmaceutical environment A degree (or equivalent) in a scientific discipline (desirable). Clear understanding of GMP or any other GxP area, regulatory and accreditation systems, and quality management. Excellent analytical thinking to evaluate information and understand complicated issues. Excellent interpersonal skills ...

active role in solving quality issues, continuous improvement programmes, and other quality and/or Food Safety projects Carry-out audit activities such as GMP audits, GHP audits and Internal audits as required Additional Responsibilities Support Food Defence activities such as Horizon Scanning, facilitating communication within the site to mitigate ...

Profile Essential ~5 years’ experience in pharmaceutical or medical device manufacturing Background in production, process engineering, or quality Strong understanding of manufacturing operations in GMP environments across multiple products and processes. Excellent communication and problem-solving skills Desirable Exposure to MES or manufacturing digitalisation initiatives Quality Assurance, process improvement ...

initiatives at site level What They’re Looking For Strong experience in IT project/delivery management Experience working in GxP-regulated environments (e.g. GMP, CSV) Background supporting manufacturing or site-based systems (e.g. MES, ERP, shop floor systems) Hands-on approach to delivery (not just governance) Ability to manage ...

activities (IQ/OQ/PQ) for equipment and processes Ensure timely delivery of KPIs and departmental objectives The Person Proven experience within a GMP-regulated environment in a similar QA/Validation role Experience in equipment validations (writing reports), the ideal applicant will have process validation experience too Previous ...

system rules. Familiarity with relational databases. Experience with DC schemes. Experience with buy-in/buyout data requirements. Exposure to pensions projects such as GMP Equalisation or Pensions Dashboard. What you can expect in return A competitive salary and market leading bonus scheme with stretch targets for high performance Study ...

system rules. Familiarity with relational databases. Experience with DC schemes. Experience with buy-in/buyout data requirements. Exposure to pensions projects such as GMP Equalisation or Pensions Dashboard. What you can expect in return A competitive salary and market leading bonus scheme with stretch targets for high performance Study ...

product assessments Support product launches, data tracking and continuous improvement initiatives Maintain responsibility for site pest control and audit readiness Ensure completion of hygiene, GMP, fabrication and calibration audits through the QA team Manage microbiological sampling, swabbing and testing programmes Conduct traceability exercises and support complaint investigations Drive improvements ...

customer audits Act as key QA contact for retailer and supermarket requirements Manage non-conformance investigations, complaints, and product release decisions Drive GMP compliance and continuous improvement across quality systems Lead, coach, and develop the QA team Ensure full compliance with food safety legislation and customer standards Support NPD, trials ...

embedding Greencore, customer, and legal standards, ensuring compliance is consistently achieved and maintained. This role plays a critical part in driving improvements in GMP performance and audit readiness, helping to raise quality standards and strengthen food safety culture across the site. Role Accountabilities • Understand and apply Greencore, customer ...

boxes. What you'll be doing Owning food safety, HACCP, and BRC compliance Leading audits with confidence (not scrambling before them) Driving improvements across GMP, suppliers, and systems Managing complaints, trends, and root cause (properly) Coaching and influencing teams across the site Why this role stands out You'll have ...

rectifying issues when required Participating in team meetings and personal development sessions Testing and maintaining internal spreadsheets Supporting large projects, including Guaranteed Minimum Pension (GMP) equalisation Carrying out manual pension calculations to validate system calculations Assisting with basic system maintenance, including resetting passwords and running reports Person Specification Good organisational ...

continuous improvement across the site. What you will be doing: Lead, coach and develop the site Quality team Ensure full compliance to the FSQMS, GMP, CCPs and process controls Assure all finished products are safe, legal and produced to specification Manage customer complaints, concessions, incidents and escalations Oversee raw material ...

teams to clearly communicate the requirements for the Store and capture client requirements. The industries we serve have growing requirements for regulatory quality control (GMP, Medical Devices, ISO etc). The System Engineering role provides opportunity to develop the fully documented lifecycle to support adherence to these standards. What ...

collected for testing schedules and testing schedules are met Logging micro samples Accurate carrying out of positive release checks for all finished products GMP audits/Glass and plastic audits, including generation of improvement areas, completing database Ensure close outs of non-conformances Sampling and recording of finished product shelf ...

Produce detailed documentation including FDS, FAT reports, and user manuals Promote teamwork and contribute to a positive working culture Ensure compliance with quality standards, GMP, and health & safety regulations Support lean manufacturing and continuous improvement initiatives Undertake any additional tasks as required by the business Requirements for the role: Minimum ...

About the Company TechYard are currently recruiting on behalf of the Google platform partner, specialising in strategy and development of client solutions across GMP, GCP and Google AI. As a certified Google Cloud and Google Marketing Partner, their teams provide cutting-edge data and AI services. About the Role ...

business. The successful candidate will play a key role in maintaining and continuously improving the Quality Management System (QMS), ensuring compliance with GDP/GMP requirements, and supporting regulatory obligations in line with MHRA, Home Office, and EU regulations. This role requires a strong understanding of pharmaceutical quality systems, supplier … maintaining GDP compliance and WDA obligations Ensure continuous monitoring and improvement of the Quality Management System (QMS) Ensure compliance with MHRA, Home Office, GDP, GMP, and EU regulatory requirements Provide QA support across all departments to ensure regulatory compliance is maintained Support recall management, incident handling, and escalation processes Quality ...

agency or client side). Highly organised, calm under pressure and confident communicating performance insights. Experience in lead generation, Google Ads/Microsoft Ads, GMP or Meta Blueprint is an advantage. Why Join Us: Competitive Salary 31 days holiday, increasing to 33 days after 2 years of service plus have ...

completed Collecting micro samples as per schedule Traceability Investigations into complaints Daily auditing of CCPs Daily label checks Calibration Auditing of processing records GMP/Fabric audits Temperature checks Quality checks The nature of the role requires a flexible approach to working hours. Core working hours are: Monday to Friday ...

essential. Previous QA experience in the management of (CAPA, Deviation, Change Controls, Complaints, PQRs, Management Reviews, recalls, Strong knowledge of: Good Manufacturing Practice (GMP) and GxP EU Annex 11 21 CFR Part 11 GAMP 5 Data integrity principles and MHRA expectations Experience supporting or leading regulatory inspections and audits Required ...

Document Management System (DMS) in preparation to a migration to Veeva Vault system. This role is critical to ensuring documentation related to GMP manufacturing processes is current, compliant, and readily accessible. The System Specialist will support cleanup activities related to the DMS, manage the review and approval workflows of global … Periodic Review Monitoring: Track, monitor and update the Past Overdue Periodic Review Reported, and create monthly reports of periodic document reviews in accordance with GMP and internal procedures. Escalate overdue tasks and non-compliance issues to department leads and Quality leadership. • Translation Coordination: Oversee the translation of controlled documents ...

ensuring effective corrective action. * Approve suppliers and ensure raw material compliance through risk-based assessment and documentation review. 5. Production * Ensure Good Manufacturing Practice (GMP) standards are consistently maintained across the site. * Oversee hygiene standards and environmental monitoring programmes. * Promote a strong food safety and quality culture throughout the business. … support and training to production and operational teams. Knowledge, Skills & Experience * Minimum 3-5 years' experience in food manufacturing * Strong working knowledge of HACCP, GMP, allergen management, and UK food legislation. * Experience managing BRC audits. * Proven leadership and people management skills. * Advanced HACCP qualification. * Internal/Lead Auditor qualification. * Experience ...

through the QMS. Conduct audit trail reviews. · Perform area walkthroughs to identify and resolve non-compliance. Audit raw data, protocols and validation reports for GMP compliance. Maintain and promote audit readiness. Ensure protocols and validation reports are approved according to project schedules. Lead process audits and support GMP audit activities. … Local Quality Councils and project meetings. Provide QA SME support for Operations, QC, MSAT and Development Services. Mentor and coach business partners in GMP practices. Advise scientists on documentation and follow-up expectations. Provide out-of-hours QA support where required. Act as a GMP SME enforcing site quality processes. ...

impact digital transformation projects in the Pharmaceutical industry? This opportunity offers the chance to work on cutting-edge MES implementations and validation strategies within GMP-regulated environments in the UK. Due to upcoming project needs, we are looking for a Senior Consultant – MES & Validation (Siemens Opcenter Execution Pharma … Opcenter Execution Pharma Contribute to the definition of Validation Master Plans and overall validation strategy Review and assess validation documentation to ensure compliance with GMP requirements and project standards Evaluate the system integrator’s project methodology and assess the quality and consistency of deliverables Ensure alignment with project expectations, regulatory ...