51 to 75 of 92 GMP Jobs

clean line sign-off, collection of swabs & water samples Quality checks and then collection of finished product and raw materials for microbiological & nutritional testing Conducting various daily audits (including GMP, Glass & Plastics audits, and ensuring corrective action with the shift manager Conducting internal quality assessment panels (QAS) throughout the shift & raising issues with the senior key-op/shift manager More ❯

Ability to work independently and manage multiple priorities Solid organizational and record-keeping skills Qualifications Experience in customer technical support, ideally in the diagnostics or healthcare industry Knowledge of GMP, ISO, and other relevant quality standards Proficiency with Microsoft Office and customer support tools Education Bachelor's degree in Life Sciences, Biomedical Engineering, Medical Technology, or a related field What More ❯

Automation Engineer Location: London Our client is a gene therapy company that works with gene therapy discovery, development and GMP manufacturing. They have headquarters in London and the USA and have recently redesigned exciting new labs with cutting edge technology and the ability to work to a higher standard and increase their capacity of production. They are currently seeking an … commissioning protocols, user requirement specifications, acceptance test plans, Functional Specifications. Design Specifications, and drawings and diagrams. Work with site Quality and CSV personnel to ensure automation and control system GMP compliance. Raise and complete Quality Events, change controls, CAPAs, and Deviations for automated GMP systems and equipment into the site QMS system. Support training efforts for new equipment installations Responsible … for ensuring that own work complies with GMP, Data Integrity and GDP and is undertaken in accordance with applicable procedures Skills Required: Bachelor's degree in Engineering from an accredited university in mechanical, chemical, or electrical disciplines with minimum 5 years' experience, supporting or developing automated systems. Strong understanding of automation standards and architecture addressing batch process control, such as More ❯

for example). Working collaboratively with all operations teams within the business, such as Quality and Health and Safety to uphold the stringent protocols necessary along with adhering to GMP and Data Integrity at all times. Your background: BSc or equivalent in a Life Science discipline. Demonstrable experience in a business development role, from within the Biologics or Pharmaceutical Manufacturing More ❯

for all pension renewals Requirements: The ideal candidate must have a good DB pension's technical knowledge, ideally 5 year's experience working in a Defined Benefit, knowledge of GMP reconciliation, equalisation calculations and PPF. Excellent computer, communication, and organisation skills. Also being able to work independently as well as part of a team. An excellent opportunity for the right More ❯

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 ❯

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 ❯

instructions Streamline updates of procedures to meet set KPI's Guide project team to meet deadlines, KPI's and bring stakeholders together Your profile Min. 7-8 years of GMP experience Extensive MES knowledge (min. 7-8 years) Proven Project Management experience English mandatory, Dutch is a big plus What we have to offer At ALTEN, we offer you the More ❯

and commissioning activities. Supervise construction works. Create lifecycle documents such as URS, Risk Assessments, IOPQ. Execute and document protocols and summary reports. Perform and document tests in compliance with GMP guidelines, CFR21 Part 11, and testing procedures. Knowledge of data integrity, user access, and security settings. Participate in safety analyses such as SWIFT, HAZOP, FMEA, etc. Document quality incidents, deviations More ❯

environments. Proficiency in Dutch or French preferred. Solid understanding of incident management workflows in line with ITIL/ITSM frameworks. Pharmaceutical industry experience is a must, including familiarity with GMP environments and compliance-driven processes. Familiarity with Siemens PLCs (S7-300, S7-400, S7-1500) and PCS 7 system structure - enough to understand system flow, interpret logic, and assist in More ❯

industry trends and emerging products. In-depth knowledge of backend/middleware development using .NET languages (C++, C#, VB.NET) and proficient in Oracle Databases. Understanding of Good Manufacturing Practices (GMP). About us : At Vulcain Engineering, we transform industrial and technological challenges into opportunities. Whether you are looking for an expert partner for your projects or a stimulating environment to 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 ❯

inclusive work environment Self-motivated and proactive with the ability to take ownership of tasks and drive them to completion Good Experience in 3rd party tracking & analytics solutions, including GMP and Adobe Previous client facing media agency experience Knowledge of running Google shopping campaigns Benefits Bountiful Cow is a unique place to work. It's the best of both worlds. 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 ❯

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 NHSBT Organ and Tissue More ❯

at this time. Responsibilities: Work closely with and follow the instructions of the CSV Lead to ensure compliance with required protocols and regulations Perform all duties in accordance with GMP requirements, SOPs and controlled documents. Support the project team as they work towards execution and handover Requirements: 3+ years experience of life sciences experience Knowledge and illustrated experience of working More ❯

lifecycle to ensure work plans meet client needs effectively and align expectations. As well as playing a key role in attracting and winning new projects for ALTEN. Your profile GMP experience Experience level: medior/senior engineer (+7y of experience) Languages: English mandatory, Dutch is a big plus What we have to offer At ALTEN, we offer you the security More ❯

time and to a high quality In addition, you’ll also: Have experience in Paid Search Hands on experience with Google Ads and Microsoft Ads Possess an understanding of GMP stack, in particular Search Ads 360 Strong Excel skills Experience with running Performance Max/Shopping campaigns for retail clients Paid Social experience is desirable but not a requirement Our 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 ❯

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 ❯

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 ❯

requalification, revalidation, and periodic review activities. Acting as Subject Matter Expert for validation during Regulatory and customer inspections. Key attributes and skills: Essential: Prior experience in a Pharmaceutical/GMP environment Good understanding of Qualification & Validation lifecycles Up-to-date knowledge of current regulatory requirements and industry standards associated with Validation activities Experienced in the execution of validation and qualification More ❯