26 to 50 of 112 GMP Jobs in England

environment Desirable 1. Experience with catheter-based or similarly complex diagnostic/therapeutic devices 2. Experience managing US FDA regulatory interactions or GLP/GMP study programmes 3. Prior experience in a Series A-B medical device company What's on Offer A pivotal, high-impact role in a well ...

coach, develop and inspire technical teams. Desirable Experience within medical devices, healthcare technology or other safety-critical industries. Knowledge of IEC 62304, ISO 13485, GMP and FDA-regulated environments. Experience with cloud platforms such as Azure, AWS or GCP. Understanding of cybersecurity for connected devices and IoT systems. Exposure ...

analytics, CRO, A/B testing, and site optimisation. Awareness of DCO platforms (Flashtalking, Sizmek, Jivox, RevJet). Understanding of attribution solutions (GMP, Neustar, Visual IQ, etc.). Experience working within regulated industries (pharma experience advantageous). Additional Information Zenith International has fantastic benefits on offer ...

MedPharm Ltd in Guildford is seeking a CSV Specialist to govern and manage validated computerised systems (GxP) across the site, ensuring compliance with EU GMP Annex 11 and MHRA guidance. You will oversee the validation lifecycle (URS, IQ/OQ/PQ, reports), assess updates, perform risk assessments, and support ...

electrical schematics and technical drawings Good understanding of mechanical systems (gearboxes, bearings, conveyors, pneumatics) Knowledge of food safety standards such as BRC, HACCP, or GMP Strong problem-solving skills and ability to work independently Benefits Opportunity to work in a modern food manufacturing facility Ongoing training and development Pension scheme ...

will have experience in raw materials, technical or quality roles within food manufacturing. Bringing a strong understanding of food safety, legality, allergens, HACCP, GMP and customer codes. Being confident working with technical systems, specifications and supplier documents. You will have good analytical skills and the ability to spot risks early. ...

. Experience with process control and automated systems for production lines. Familiarilty with PID tuning for production lines. Familiarity with industry-specific regulations (HACCP, GMP, etc.) and food safety standards. Knowledge of instrumentation and process equipment . Knowledge of Java, Python, C++ and VB Scripting Familiarity with Flow Charts ...

Catalent Swindon site seeks an Associate Director, QMS & Compliance to lead the Quality Management System and regulatory affairs, ensuring GMP/FDA/MHRA compliance and continuous improvement at a leading biologics/pharmaceutical operations hub in Swindon, UK. You will develop high-performing teams, manage QMS budgets, and partner ...

backup/restore, or diagnostics standards for complex software-enabled products.Experience working in regulated or validated environments, including exposure to SAT, IQ/OQ, GMP, or automation validation practices.Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether ...

/restore, or diagnostics standards for complex software-enabled products. Experience working in regulated or validated environments, including exposure to SAT, IQ/OQ, GMP, or automation validation practices. Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether ...

Management System (QMS) design, transformation and implementation.In this role, you will advise clients across pharmaceutical, biotechnology and related life sciences environments, supporting compliance with GMP, GDP, GCP and GLP requirements. You will lead and deliver quality transformation initiatives, combining strong hands‐on expertise with a pragmatic, client‐focused consulting approach.What … clinical and distribution environments.Conducting process mapping and gap assessments, and supporting the rollout of new or enhanced systems aligned to global regulatory standards (including GMP, GDP, GCP, GLP, FDA 21 CFR 210/211, EU GMP/EudraLex, ICH Q7/Q10).Authoring, reviewing and maintaining quality policies, standards, SOPs ...

Management System (QMS) design, transformation and implementation.In this role, you will advise clients across pharmaceutical, biotechnology and related life sciences environments, supporting compliance with GMP, GDP, GCP and GLP requirements. You will lead and deliver quality transformation initiatives, combining strong hands‐on expertise with a pragmatic, client‐focused consulting approach.What … clinical and distribution environments.Conducting process mapping and gap assessments, and supporting the rollout of new or enhanced systems aligned to global regulatory standards (including GMP, GDP, GCP, GLP, FDA 21 CFR 210/211, EU GMP/EudraLex, ICH Q7/Q10).Authoring, reviewing and maintaining quality policies, standards, SOPs ...

LGBTQ+ business community. Please do not contact the recruiter directly. Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description How will you make ...

within a QA, Quality Assurance, or Quality Control role. Experience within the food manufacturing industry is essential. Good understanding of HACCP, Food Safety, and GMP standards. Strong attention to detail and excellent record-keeping skills. Confident communication skills and ability to work collaboratively. Ability to work independently and make informed ...

people flow within production environments -Experience across food, chemical, industrial or pharmaceutical sectors -Ability to develop site masterplans and concept studies -Knowledge of GMP or similarly regulated design environments (desirable) -Strong communication skills, and the ability to work across multidisciplinary teams We appreciate your ...

beneficial.Experience working with health authorities and supporting regulatory discussions and responses, underpinned by a solid understanding of global development and post-approval requirements, GMP expectations and regulatory practices in at least one ICH region.Able to analyse technical data, create clear regulatory narratives, identify gaps early and manage traceable content across ...

complex technical issues and simplifying them for audiences ranging from practitioners to executives. Responsibilities: Partner with Account teams to drive adoption of our Ads, GMP, and our client solutions with our largest Agencies and Partners (A/Ps). Utilize designingand storytelling to design data-driven marketing architectures and long ...

complex technical issues and simplifying them for audiences ranging from practitioners to executives. Responsibilities: Partner with Account teams to drive adoption of our Ads, GMP, and our client solutions with our largest Agencies and Partners (A/Ps). Utilize designingand storytelling to design data-driven marketing architectures and long ...

ensure the continued operation of the calibration systems and equipment within the company. To ensure that all work is performed in full compliance with GMP, SOPs, FDA, MHRA, work instructions and established safety standards. The primary focus of the role will be instrumentation and calibration but the candidate will ...

conforming products, QA holds and product releases. Assisting with and carrying out audits, including BRC internal audits, Glass and Plastic audits, CCP checks, GMP inspections, product and process audits, temperature monitoring, pH testing, cleaning audits and metal detection checks. Monitoring equipment performance through internal calibration of scales, pH meters ...

Supporting Bakery and Packing teams with the correct completion of CCP and food safety checks - Checking packaging, labels, date codes and product identification - Monitoring GMP, hygiene and general factory standards - Supporting the control of non-conforming product and escalation of food safety or quality issues Our Perfect Worker Our perfect ...

regulated environment. You will lead technical activities across serialisation, diagnostics, data integrity and validation support, contributing to compliant, efficient manufacturing operations. Prior experience in GMP-like settings is highly desirable. #J-18808-Ljbffr ...

pipeline management. Full UK driving licence and willingness to travel nationally. Desirable: Experience in pharmaceutical packaging, labels, folding cartons, medical devices or GMP-regulated environments. What We Offer Competitive bonus Car allowance 25 days' holiday International career opportunities Modern manufacturing environment Free onsite parking Location: Royston (SG8 5HN) Ready ...

electrical experience within the FMCG sector. Experience and a good understanding of PLCs, fault finding, 3 phase, DC motors, relays, contractors, sensors, and drives. GMP experience. ...

ready, and completed right the first time. You will also support the management of deviations and data integrity requirements, ensuring all activities comply with GMP and regulatory expectations. As a valued technical specialist, you will work closely with the Validation Team Leader and other stakeholders to deliver projects safely, compliantly ...