Chalfont St. Giles, Buckinghamshire, South East, United Kingdom
TREVETT PROFESSIONAL SERVICES LTD
development life cycle methodologies, 21 CFR Part 11, and GAMP. Development of detailed specification, engineering documents, SOP and operating standards. Ownership and administration of process control automation in a GMP regulated manufacturing setting. Lead technical root cause analysis, incident investigations, and troubleshooting on process control issues related to electrical, instrumentation and control systems. Design and test of newly installed and More ❯
with this role involving standing 60% to 100% of the time and lifting heavy weights. Knowledge and experience using computer software including ERP system. and possibly Experience in a GMP environment would be advantageous. Certified to handle and ship Dangerous Goods or willingness and ability to be trained immediately. Supplier account management. Working with couriers, customs and brokers. Experience delivering More ❯
in a fast-moving environment providing excellent service to clients and third parties with a desire to succeed at accomplishing challenging objectives. Desirable Criteria Knowledge of and experience with GMP Reconciliation/Equalisation calculations. Practical knowledge of the Pension Protection Fund (PPF). Circumstances Working hours: Monday to Friday, 37.5 hours per week with additional hours as and when required. More ❯
technical and mathematical skills. Desirable knowledge and skills Possess a strong knowledge of Google Marketing Platform, including Google Tag Manager (GTM). Able to perform high-level analysis within GMP platforms such as GA4 and Floodlight to extract insights and support marketing efforts. Utilise programming languages (e.g., Python, R) and database management tools (e.g., SQL) Awareness of customer data SaaS More ❯
history: Relevant degree in Scientific, Engineering, or a similar subject. Extensive industry experience in validation, engineering, or operations within a cGMP environment. A working knowledge and practical experience with GMP utilities, equipment, DIA, and CSV. Key Words: Senior Validation Engineer/Biotech/Validation/cGMP/CQV/DIA/CSV/Qualification Protocols/Equipment Compliance/Data More ❯
looking to identify the following on your profile and past history: 1. Previous experience working within a Pharmaceutical or Food manufacturing environment. 2. Proven industry experience in GMP (GoodManufacturingPractice) and GDP (Good Distribution Practice). 3. A working knowledge and practical experience with SAP or equivalent ERP systems. More ❯
and implement Siemens automation solutions (PCS7, SIMATIC SCADA, TIA Portal, MES). Program and troubleshoot PLC (S7-1500, S7-1200) and DCS for optimized process control. Ensure compliance with GMP, GAMP, FDA guidelines in automation projects. Oversee commissioning, validation, and maintenance of automation systems. Collaborate with process engineering, IT, and quality teams to enhance automation efficiency. Stay updated on emerging … . Required Technical Skills: 5+ years in pharmaceutical automation with Siemens systems. Strong expertise in PCS7, SCADA, MES, and PLC programming (TIA Portal) . Deep knowledge of regulatory standards (GMP, GAMP, FDA) . Experience managing automation projects, validation, and troubleshooting . More ❯
Understanding of distributed systems concepts. Experience with Python for data processing or image analysis. Background or interest in biology, lab automation, or scientific instrumentation. Any experience with regulated environments (GMP, HIPAA, etc.) Any experience with UI/product design processes and tools (wireframes, mockups, looks-like prototypes, etc.). Why You'll Love Working Here Impact : Your work will directly … complex problems at the intersection of software, hardware, and biology-you'll constantly learn and develop new skills. Autonomy : You'll have the freedom to shape our approach to GMP readiness, with support from a talented cross-disciplinary team. Team : Work with the best engineers and scientists in a collaborative environment where diverse perspectives drive innovation. Salary and Benefits Competitive … re building a team that enjoys moving fast, strives for continuous improvement through learning from mistakes, and is passionate about work that contributes to solving real world problems. No GMP experience? No problem! We want someone who is motivated to deliver an innovative product into a regulated space with creative, efficient solutions. If you're excited about solving interesting problems More ❯
work environment Self-motivated and proactive with the ability to take ownership of tasks and drive them to completion Desirable: Good Experience in 3rd party tracking & analytics solutions, including GMP and Adobe Previous client-facing media agency experience Knowledge of running Google shopping campaigns Experience on retail media platforms such as Criteo and CitrusAd Benefits: Uncounted holiday & wellbeing (Star) days More ❯
product. Verifying finished product label information and managing on the online label verifier, including reel changes and troubleshooting. Develop in-depth knowledge of automatic labeller and verifier machine. Formal GMP and process control document completion. Requirements: Ideally have experience of working within a fast- paced food manufacturing environment. A good level of both written and verbal English. Ideally have Level More ❯
Attleborough, Norfolk, East Anglia, United Kingdom
Galaxy Personnel
product. Verifying finished product label information and managing on the online label verifier, including reel changes and troubleshooting. Develop in-depth knowledge of automatic labeller and verifier machine. Formal GMP and process control document completion. Requirements: Ideally have experience of working within a fast- paced food manufacturing environment. A good level of both written and verbal English. Ideally have Level More ❯
that the relevant documents have been completed, e.g., hold log, non-conformance log. Reporting any complex issues to QA Supervisor. Hygiene Audits, micro swabbing, and micro sampling product Formal GMP and Process Control document completion About the shift pattern: This Monday - Friday QA role is based in our technical department but working in all areas of the factory as required More ❯
informatics software applications and the vision for modernization in this space Ability to travel for customer meetings and presentations up to 40% Nice to Have Industry experience with QC, GMP quality content, training management, quality systems processes, or manufacturing Leadership of global Sales teams to drive opportunities with intensity Seasoned at developing and maintaining relationships with executive-level stakeholders Published More ❯
Qualifications Candidates must have proven experience of automation delivery on multiple projects in the pharmaceutical industry. Knowledge of industry standards and systems is essential, alongside a good understanding of GMP requirements for automated systems. The role requires delivery of results on time, in accordance with client standards and health and safety procedures. The successful candidate will be a self-starter More ❯
Billingham, Stockton-on-Tees, County Durham, United Kingdom
PM Group
Qualifications Candidates must have proven experience of automation delivery on multiple projects in the pharmaceutical industry. Knowledge of industry standards and systems is essential, alongside a good understanding of GMP requirements for automated systems. The role requires delivery of results on time, in accordance with client standards and health and safety procedures. The successful candidate will be a self-starter More ❯
Are you looking for an exciting opportunity to shape our test management process as we transition to a DevSecOps approach? You'll also support current waterfall-based test activities to ensure the delivery of high-quality products into production.This role More ❯
Job summary Are you looking for an exciting opportunity to shape our test management process as we transition to a DevSecOps approach? You'll also support current waterfall-based test activities to ensure the delivery of high-quality products into More ❯
toxicological assessment, extractable and leachable analysis, medical device manufacturing processes, and biocompatibility assessment methodology Basic knowledge of FDA and international medical device regulations/directives and working knowledge of GMP/ISO/GLP guidelines as applied to medical device testing and documentation. Have the ability to work with people and teams in a complex, changing environment and be able More ❯
Developing specifications and leading multidisciplinary 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 You’ll Be Doing Designs, defines More ❯
building and managing cloud-based data pipelines to drive successful business outcomes for large organisations. Your expertise in digital media and marketing platforms, such as Snowflake, Azure, AWS, GCP, GMP, Adobe, and Tealium, enables you to develop scalable data solutions with a customer-centric focus. With a strong technical background and the ability to collaborate effectively with internal and external More ❯
plans that can be presented clearly at every level WHAT WE ARE LOOKING FOR Have extensive, relevant programmatic experience (Google Ads (Display/Video), DSPs (e.g. Adform, Tradedesk, DV360), GMP and Analytics Have experience with, and gain a lot of energy from, guiding other people Have experience with the Dutch and/or Nordic publisher landscape Are analytical, flexible and More ❯
and delivers solutions for wide-ranging issues and a varied customer base. Project & Data Solutions delivers the right, cost-effective strategies and solutions for the following: Guaranteed Minimum Pension (GMP) projects Auditing data, benefits and calculations Bulk data rectification and benefit (re-)construction Data cleansing and improving electronic data Supervising the data workstreams for de-risking projects so data is More ❯
Stockport, Greater Manchester, North West, United Kingdom Hybrid / WFH Options
Vox Recruitment Ltd
and experience ideally across all digital media channels but in particular paid search. You will have excellent knowledge of bid management and core technology platforms such as Google Analytics, GMP Platform, SA360 for example. Data analysis and an understanding of the strategic application of digital marketing channels will be a strength. More ❯
media analytics (agency background preferred) Strong knowledge of measurement frameworks incl. attribution and MMM Proficiency in SQL, Python, R, and leading data viz platforms (e.g., Tableau, Looker) Familiarity with GMP, Meta, CDPs/DMPs, ad servers, and tagging solutions Experience with cloud platforms (AWS/Azure) Confident team leadership and stakeholder management Bonus Points: Knowledge of clean rooms, first-party More ❯
media analytics (agency background preferred) Strong knowledge of measurement frameworks incl. attribution and MMM Proficiency in SQL, Python, R, and leading data viz platforms (e.g., Tableau, Looker) Familiarity with GMP, Meta, CDPs/DMPs, ad servers, and tagging solutions Experience with cloud platforms (AWS/Azure) Confident team leadership and stakeholder management Bonus Points: Knowledge of clean rooms, first-party More ❯