26 to 50 of 57 Permanent GMP Jobs

Participate in Technical audits including customer and Group Technical, ensuring all relevant raw material information is available and completed in the required timescale Audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence, effectively communicated to enable the operational teams to take the appropriate and necessary corrective action & to follow More ❯

Participate in Technical audits including customer and Group Technical, ensuring all relevant raw material information is available and completed in the required timescale Audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence, effectively communicated to enable the operational teams to take the appropriate and necessary corrective action & to follow More ❯

checks, supplier and internal non-conformance, customer complaint investigations, glass & plastic audits, and fabrication audits. - Supporting the training of staff and verification against CCPs, policies and procedures. - Conducting internal GMP audits across departments and conducting hygiene verifications. - Assisting with external audits. The role will be a mix of factory and office-based work to meet the needs of the business More ❯

negotiation, and presentation skills. Highly self-motivated, organised, and target-driven. Experience with clients in life sciences, healthcare, or education. Knowledge of cleanroom or controlled environment standards (e.g., ISO, GMP). Technical or engineering background advantageous. Benefits Competitive base salary of £40,000 + performance-related bonus Hybrid working: 3 days in office/2 days from home Pension scheme More ❯

follow-up, and root cause investigations. What We’re Looking For: 5+ years of experience in Site Reliability Engineering or a related field. Hands-on experience with Biosafety and GMP environments. Strong foundation in Lean Six Sigma principles. Proven problem-solving skills with a knack for performance tuning. Effective communicator and team player. Formal education in an engineering-related discipline. More ❯

follow-up, and root cause investigations. What We’re Looking For: 5+ years of experience in Site Reliability Engineering or a related field. Hands-on experience with Biosafety and GMP environments. Strong foundation in Lean Six Sigma principles. Proven problem-solving skills with a knack for performance tuning. Effective communicator and team player. Formal education in an engineering-related discipline. More ❯

equivalent experience in Controls, Mechanical/Electrical, or Software Engineering. Proven experience in Systems Engineering, specification writing, and validation. Strong organisational, communication, and coordination skills. Familiarity with regulatory standards (GMP, ISO, Medical Devices). Experience with MS Project, MS Office, Visio, and 3D CAD or AutoLab. What you'll get in return Competitive salary and benefits package. Opportunity to work More ❯

usage, and downtime. Safety and Compliance Adhere to all required safety practices, including use of PPE, lockout/tagout, and machine guarding procedures. Ensure compliance with facility food safety (GMP), product safety, and quality standards. Engage emergency stop systems and follow protocols during maintenance or mechanical troubleshooting. Communication and Collaboration Effectively communicate with oncoming shift, supervisors, quality control, and support More ❯

our team in Bedford Park, IL. What you ll be doing: The Controls Systems Engineer is responsible for maintaining instrumentation and control systems in support of plant production, quality, GMP and safety goals. Ensuring the instrumentation, control systems, and documentation (and validation or PSM where required) are capable of supporting the quality and production goals of the assigned unit in More ❯

act as point of contact for the Archives facility (Archives Champion) for documentation queries. This will include preservation notices management, capacity monitoring, destruction management and liaison for archive documentation GMP queries. Qualifications & experience: · SVQ Level 3: Highers/higher national certificate/apprenticeship or equivalent More ❯

act as point of contact for the Archives facility (Archives Champion) for documentation queries. This will include preservation notices management, capacity monitoring, destruction management and liaison for archive documentation GMP queries. Qualifications & experience: · SVQ Level 3: Highers/higher national certificate/apprenticeship or equivalent More ❯

Pensions data and transformation projects. You'll work directly with clients to analyse, cleanse and migrate data, design and test Pension calculations, and support key industry programmes such as GMP rectification and equalisation. Key Responsibilities Analyse complex Pensions data using SQL and Excel Deliver data mapping, migration and cleanse activities Produce and test calculation specifications based on scheme rules Present More ❯

act as point of contact for the Archives facility (Archives Champion) for documentation queries. This will include preservation notices management, capacity monitoring, destruction management and liaison for archive documentation GMP queries. Qualifications & experience: · SVQ Level 3: Highers/higher national certificate/apprenticeship or equivalent More ❯

patient outcomes. About the Role We're hiring a QA Compliance Manager to lead a team focused on maintaining and enhancing the Quality Management System (QMS) in compliance with GMP, ISO 9001, ISO 13485, and other regulatory standards. Reporting to the Head of Quality, you'll oversee internal audits, batch record reviews, CAPA systems, and customer audits, while also supporting … opportunity with potential Qualified Person (QP) sponsorship for the right candidate. Key Responsibilities: Lead and develop the QA Compliance team Maintain and improve the QMS in line with EU GMP and ISO standards Oversee internal audits, CAPA management, and batch documentation review Host customer audits and support regulatory inspections Drive continuous improvement and contribute to strategic quality initiatives Support training … change control, and compliance projects Candidate Requirements Essential: Degree in a scientific discipline (e.g. Chemistry, Biology, or related field) 10+ years' experience in GMP-regulated environments Strong leadership and people management skills In-depth knowledge of EU cGMP, ISO 9001, and ISO 13485 Experience supporting or conducting batch release under QP supervision Lead Auditor training and a proactive approach to More ❯

Celonic ist eine "Pure Play" Biologics Contract Development Manufacturing Organization (CDMO). Celonic hat es sich zur Aufgabe gemacht, ihre Kunden, in erster Linie kleine bis große Biotech-Unternehmen, dabei zu unterstützen, lebensrettende und -verbessernde Medikamente unter Einsatz innovativer Bioprozesstechnologien More ❯

Celonic ist eine "Pure Play" Biologics Contract Development Manufacturing Organization (CDMO). Celonic hat es sich zur Aufgabe gemacht, ihre Kunden, in erster Linie kleine bis große Biotech-Unternehmen, dabei zu unterstützen, lebensrettende und -verbessernde Medikamente unter Einsatz innovativer Bioprozesstechnologien More ❯

Set Proven leadership in digital performance, measurement and data strategy roles. Hands-on experience with MMM, incrementality testing and advanced attribution. Strong understanding of ad tech and martech ecosystems (GMP, GA4/BigQuery , Meta CAPI, server-side GTM etc.). Fluent in using data to tell compelling stories and influence both internal teams and C-suite clients. Success Indicators (First More ❯

instructions, change controls, deviations, investigations, 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 career with us. At Piramal … to performing the relevant disposition 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 More ❯

the functioning of the QMS, providing oversight to key stakeholders alike (including senior staff members). Accountability across (but not limited to); change control, stability, documentation control, internal audits, GMP, supplier approval, complaints, PQRs, NPI, route cause analysis and controlled drug returns. Ensuring compliance/correct documentation practices, i.e batch records, laboratory tests and quality agreements too. Overseeing supplier verification … batch review process. Keeping abreast of evolving UK & EU retained regulations (for the purposes of pharmaceutical and/or food/ingredients manufacturing). To ensure compliance with EU GMP standards & BRC food safety requirements. Managing the preparation process (and heavily involved in hosting activities) for MHRA inspections, customer (third party audits) and acting as the lead person. Enrsuring quality … bodies. Deputising for the HOQ when required. The Person:- The ideal Candidate will hold a degree in a STEM related subject Experience managing QA team/s in an GMP/Pharmaceutical setting. Management experience essential (will consider Team Leader or similar). Experienced in batch review and batch release Experience in auditing and audit hosting Experience in CAPA, deviations More ❯

pharmaceutical sector, we want to hear from you! Key Responsibilities: Support the Quality team in maintaining the organisation's Quality Management System (QMS). Ensure compliance with ISO 9001, GMP, and GDP standards, as well as internal procedure Raise non-conformances, deviations, and change requests, ensuring all trackers are meticulously maintained. Manage the supplier controls system, including evaluations and assessments. … Looking For: Proven experience in quality assurance, specifically in a pharmaceutical or healthcare setting. RP qualification. Being named on a Wholesale Distribution Authorisation (WDA). Strong knowledge of GDP, GMP, and ISO standards. Excellent organisational and communication skills. Ability to work independently and collaboratively in a team environment. A proactive approach to problem-solving and continuous improvement. More ❯

Systems Manager Upperton Pharma Solutions is a Nottingham-based CDMO that specialises in the development and manufacture of pharmaceutical products, providing a complete service from early-stage feasibility to GMP clinical manufacture. Formulations cover a range of delivery routes, typically including oral (tablets & capsules), nasal and inhaled. Continued growth and investment into the business has led to the creation of … exciting new job opportunities; in our new GMP Manufacturing headquarters in Beeston, Nottingham. Upperton Pharma Solutions is undergoing a period of significant expansion to meet international customer demand and offer a comprehensive drug development portfolio, so now is a great time to join our team. Reporting to the Quality and Compliance Director this role will be responsible for leading the … support the growth of the business and deliver a compliant IT platform for business-critical systems and processes. Main duties and responsibilities: Ensure compliance with the company quality systems, GMP requirements and all regulatory body requirements. Responsible for ensuring all computerised systems at Upperton remain in a qualified state in accordance with the validation/qualification schedule Responsible for ensuring More ❯

Operation and Maintenance of Automation Systems Overview: Oversee the preventive and corrective maintenance, troubleshooting, and lifecycle management of all site automation systems, ensuring reliability and data integrity in a GMP environment. Responsibilities Ensure timely response and resolution of automation-related breakdowns and deviations. Maintain system documentation (architecture, configuration, change records) in compliance with GMP. Plan and oversee execution of preventive … own Computerized System Validation (CSV) Overview: Ensure all automation systems are validated and maintained in accordance with internal policies and regulatory expectations (GAMP 5, 21 CFR Part 11, EU GMP Annex 11). Responsibilities Oversee CSV activities for new and existing systems. Ensure changes are managed under the site change control process. Partner with QA and Validation to maintain inspection … preparation, execution and reporting of GxP activities. Your Profile Master's degree in Automation Engineering, or a related field. At least ten years of experience in a pharma/GMP regulated environment. Strong background in either PLC, SCADA, DCS or MES; management experience highly preferred. Leadership & Management Skills Strong people leadership and coaching skills; ability to develop technical talent. Able More ❯

Must-Have: 8 + years of experience working in an FDA-regulated, GMP-related environment. Pharma, Biotech, Medical Device industry. Implementation and change management of QMS (Quality Management System) and LIMS (Lab Information Management System). Comprehensive knowledge of GAMP5, 21 CFR Part 11, and EU Annex 11 as well as FDA 21 CFR Parts 210/211 (cGMP), ICH … validation activities are executed in accordance with internal procedures and standards and meet all regulatory requirements. Contributes expertise and provides guidance in 21 CFR Part 11, GAMP5, and EU GMP Annex 11 requirements and data integrity principles and requirements as well as participates in assessments. Develops and evaluates quality processes and system standards to ensure compliance with company standards and More ❯

day: Responsible, Responsive, Resilient, and Respectful . Were currently recruiting for a Manufacturing Equipment & Systems Specialist to join our Manufacturing Team . In this role, you willensure compliance of GMP Equipment & Systems within the manufacturing department enabling efficient batch delivery against production schedule in line with GMP, safety and environmental requirements, playing a key part in advancing our mission and … of QMS records for equipment and Systems We are Looking For: A-Level, preferably science based with previous industrial experience Graduate in STEM subject (preferred) Experience working in a GMP environment Experience working with of Cell & Gene therapy manufacturing equipment and systems. e.g. bioreactors, chromatography, clean rooms etc. Ability to travel across all Oxfordshire sites Willingness to working within Cleanroom More ❯

Trackwise, Veeva Quality Docs, ALM, SmartLab, Empower an advantage. Essential Skills: Minimum 5 years experience in a Pharma/Biotech environment. Strong knowledge of 21 CFR Part 11, EU GMP Annex 11 principles. Ability to write and execute Change Controls, Work Items and CAPAs. Experience implementing changes for IT applications in a GMP environment. Ability to write SOPs and other More ❯