1 to 25 of 28 GMP Jobs with Hybrid or WFH Options

Ensures that there are robust processes in place for the review and release product for GLP and GCP studies. Ensures appropriate quality oversight of GMP activities performed by the Product Development teams at Dechra or CDMOs and contract laboratories. This may include review and approval of protocols, reports, methods, master more »

the management and improvement of quality systems processes to ensure both EU and US regulatory compliance to relevant company standards and Good Manufacturing Practice (GMP). The successful applicant will: Implement and monitor established policies and procedures to ensure compliance with necessary regulatory bodies in the areas of: Corrective and … Work in accordance with Company Quality Standards, procedures and processes and comply with the requirements of Good Documentation Practice (GDP) and Good Manufacturing Practice (GMP). Deputise for Senior Quality Systems Engineer when required, to ensure progression of departmental commitments. We are looking for someone who has: Minimum A level … Directive MDD 93/42/EEC Knowledge of FDA QSR Part 820 Computer literate to include MS Word, Excel and MRP Knowledge of GMP and audits Ability to work with minimal supervision and use initiative. Good interpersonal skills and the ability to communicate well in English both written and more »

the management and improvement of quality systems processes to ensure both EU and US regulatory compliance to relevant company standards and Good Manufacturing Practice (GMP). The successful applicant will: Implement and monitor established policies and procedures to ensure compliance with necessary regulatory bodies in the areas of: Corrective and … Work in accordance with Company Quality Standards, procedures and processes and comply with the requirements of Good Documentation Practice (GDP) and Good Manufacturing Practice (GMP). Deputise for Senior Quality Systems Engineer when required, to ensure progression of departmental commitments. We are looking for someone who has: Minimum A level … Directive MDD 93/42/EEC Knowledge of FDA QSR Part 820 Computer literate to include MS Word, Excel and MRP Knowledge of GMP and audits Ability to work with minimal supervision and use initiative. Good interpersonal skills and the ability to communicate well in English both written and more »

System by supporting global metrics generation and ‘lessons learned from audit/inspection’ · Cover GxP related Functional Areas, specifically thus related to GCP, GVP, GMP and CSV. · Collaborate with the respective Functional Area Heads/representatives · Collaborate with the respective Global and Regional Quality Leads and functions · Ensure the establishment more »

providing direction and leadership to staff to ensure a quality mindset is embedded in the business Requirements: Expert in GCP with working knowledge of GMP 5 years experience in a QA Manager role within a CRO, Biotech or Pharma company Contract: Hours: 3 days a week - can worked across more »

have requirements: 2-5 years’ experience working with MES/EBR or similar systems in the life sciences industries. Experience deploying MES in a GMP environment, configuring Recipes, MBR’s, Materials, BOMs, Order Management, Equipment management, Batch Review/Approval and other typical components. A background in one or more more »

experience leading IT at a senior management level • Track record of delivering results quickly • Experience in delivering IT services to customers • Work in a GMP or highly regulated environment Preferred Experience: • Experience of agile product development • Experience of Lean Six Sigma • Infrastructure delivery (networking, hardware) to customers • Experience with data more »

development with an understanding of the product life cycle ideally in laboratory automation, or pharmaceutical manufacturing environment following ISO/IEC and/or GMP standards though candidates from other industries will also be considered Hands on experience in electrical engineering in prototyping, engineering, design and testing Working knowledge of more »

development with an understanding of the product life cycle ideally in laboratory automation, or pharmaceutical manufacturing environment following ISO/IEC and/or GMP standards though candidates from other industries will also be considered Hands on experience in electrical engineering in prototyping, engineering, design and testing Working knowledge of more »

engineering or similar. Substantial demonstrable experience leading a company through ISO9001/13485 relating to medical device instrumentation development and manufacture. Further exposure to GMP manufacture for biological products would be desirable. Comprehensive experience with "quality management" within a technology company including instilling a quality-focused culture and maintainable approach more »

as part of the remuneration. Experience: Experienced project engineer or project manager in a pharmaceutical setting A strong understanding and hands on experience of GMP Engineering or validation experience is essential Exposure to the full validation lifecycle and the ability to walk through the full CQV phase Hands on experience more »

and supply chain as well as external partners like CDMOs to achieve objectives and ensure adequate product availability for launch. Ensure compliance with regulatory & GMP/GDP requirements for generic & specialty drug launches in relevant markets. Establish key performance indicators (KPIs) to track launch performance and evaluate post launch success more »

to respond to change environments and high growth, high pressure environments. Experience in managing stakeholders. Ability to track and report issues. Experience & understanding of GMP, FDA & TGA Quality requirements. Culture & Benefits We are fuelled by our commitment to sustainability, quality, efficiency, and an unwavering passion for our customers. Championing solutions more »

background and ideally Team Leading people working on similar projects as listed below:- Skills and experience:- - Pensions Data Transfer - Client Onboarding - Implementation - System Configuration - GMP - BIBO - Buy in - Buy out - Pension projects Unique culture, fully diverse and inclusive, very supportive, with ability to grow and become senior manager. Responsibilities: Takes more »

similar role. Paid, owned, website, & commerce data experience. Strong knowledge of key digital platforms, CRM, data and web analytics providers, including Adobe Marketing Cloud, GMP, GCP, Meta and other partners. Strong knowledge of data management, analytics with experience of deploying data & analytics projects across large accounts. Have managed multi- million more »

to demonstrate the ability to learn the technical aspects of processes. Able to show an understanding and willingness to comply with all food standards (GMP, health & safety etc.) consistent with working in a world class food manufacturing environment. WE SUPPORT AND CARE FOR OUR EMPLOYEES BY PROVIDING YOU WITH We more »

and equipment automationsystems at our Holmes Chapel site. You'll provide hardware and softwaresupport, resolve breakdowns, implement preventative maintenance, and ensurecompliance with GMP (Good Manufacturing Practice), EHS, and company standards.Your role also involves supporting computer system validation, qualityimprovement initiatives, and training other team members. This is a hands-onrole where … support to maintain system performance. Provide hardware,software, and coding support to maintain system performance. Resolve equipmentbreakdowns and conduct root cause analysis. Ensure compliancewith GMP, EHS, and company standards. Support computersystem validation and lifecycle management. Contribute toengineering best practices and project execution. Train team memberson equipment, systems, and procedures. Automation more »

and equipment automationsystems at our Holmes Chapel site. You'll provide hardware and softwaresupport, resolve breakdowns, implement preventative maintenance, and ensurecompliance with GMP (Good Manufacturing Practice), EHS, and company standards.Your role also involves supporting computer system validation, qualityimprovement initiatives, and training other team members. This is a hands-onrole where … support to maintain system performance. Provide hardware,software, and coding support to maintain system performance. Resolve equipmentbreakdowns and conduct root cause analysis. Ensure compliancewith GMP, EHS, and company standards. Support computersystem validation and lifecycle management. Contribute toengineering best practices and project execution. Train team memberson equipment, systems, and procedures. Automation more »

and equipment automationsystems at our Holmes Chapel site. You'll provide hardware and softwaresupport, resolve breakdowns, implement preventative maintenance, and ensurecompliance with GMP (Good Manufacturing Practice), EHS, and company standards.Your role also involves supporting computer system validation, qualityimprovement initiatives, and training other team members. This is a hands-onrole where … support to maintain system performance. Provide hardware,software, and coding support to maintain system performance. Resolve equipmentbreakdowns and conduct root cause analysis. Ensure compliancewith GMP, EHS, and company standards. Support computersystem validation and lifecycle management. Contribute toengineering best practices and project execution. Train team memberson equipment, systems, and procedures. Automation more »

product.The role will be joining the UK team, as a senior individual contributor and part of a global team.Other essential responsibilities include:Management of GMP and GDP complianceManagement of complaints, CAPAs, risk assessments, and validation protocolsReview and manage the QMS systemAble to manage non-compliance issues and escalate when neededHave … the requirement will be that you are able to travel to West London site and to supplier sites.It is a must that you have GMP and GDP experience.The role will be joining a team which is integral to the business and requires strong communication skills. The team are close-knit more »

role will be joining the UK team, as a senior individual contributor and part of a global team. Other essential responsibilities include: Management of GMP and GDP compliance Management of complaints, CAPAs, risk assessments, and validation protocols Review and manage the QMS system Able to manage non-compliance issues and … requirement will be that you are able to travel to West London site and to supplier sites. It is a must that you have GMP and GDP experience. The role will be joining a team which is integral to the business and requires strong communication skills. The team are close more »

company or CRO Experience on CMC documentation for respiratory devices is important Experience in Drug product development from early to late stage inclusive of GMP/clinical supply manufacture Experience with regulatory documentation for CMC activities on drug substance, drug product both towards FDA and EMA is mandatory Solid experience … with working in a regulated environment under GxP and with adherence to Company SOPs, policies and guidelines Updated knowledge of ICH GMP is required Excellent communication, presentation, and interpersonal skills. Self-driven and motivated team player Familiar with working in a virtual set-up Fluent in written and spoken English more »

products reach every corner of the globe with precision and efficiency. Be the guardian of quality, ensuring every launch meets the gold standard of GMP and GDP regulations. Tackle challenges head-on, turning obstacles into opportunities for innovation and growth. Keep stakeholders in the loop with your expert communication skills … Business, Life Sciences, Engineering). Strong experience in the pharmaceutical realm, where you've honed your project management skills. A deep-seated understanding of GMP and GDP guidelines. A proven track record of launching products would be advantageous. Great communication skills, coupled with the ability to navigate complex challenges with more »

Systems, distributed control system, computer validation, CSV, computer system validation, application software, software, hardware, system software, system hardware, automated production equipment, cGMP, cGMP environment, GMP, Good Manufacturing Practices, Manufacturing, Switzerland, Ireland, UK, Netherlands, Austria, Biopharmaceutical, pharmaceutical, GMP environment, sterile manufacturing, API, aseptic processing, Electrical engineering, pharmaceutical manufacturing, capital investment, project more »

build brighter futures for colleagues, clients and communities. The role will form part of the projects team with the current focus being around delivering GMP Equalisation projects on the proposition to clients, which can incorporate or lead onto being involved in de-risking projects for clients over time. This is … with internal teams to deliver a streamlined service to other lines of business. Directly involved with the management of more junior colleagues within the GMP Equalisation team, including supporting with performance reviews, training, and personal development plans. Develop skills to support on various consulting aspects of GMP projects and have … in Pensions, with a focus on Technical aspects and solid exposure to consultants and broader client support teams. Experience of technical calculations required for GMP Rectification and Equalisation projects. more »