Energy Jobline ZR
Quality Manager/Responsible Person - Pharmaceuticals in Gloucester
Energy Jobline ZR, Gloucester, Massachusetts, us, 01931
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Job Description
Quality Manager/Responsible Person - Pharmaceuticals - Gloucester\n\nSmart4 Sciences are proud to partner with an established and internationally recognised pharmaceutical company, renowned for their focus on the development, licensing and distribution of high-quality injectable medicines. With almost five decades of trusted service supplying the NHS, private healthcare, and global markets, they continue to lead in injectable and infusion therapies\n\nWe're now supporting them in hiring an experienced Quality Manager/Responsible Person (RP) to lead and continually improve the UK Quality Management System, uphold licence compliance, and embed GDP and ISO9001 best practice across their UK wholesale distribution operations.\n\nKey Responsibilities:\n\nManage and develop the UK Quality Management System (QMS) and eQMS, ensuring documentation, policies and procedures remain compliant and effective.\nMaintain WDA(H), GDP and ISO certifications; host regulatory inspections and manage responses through to closure.\nOversee internal audits, supplier audits and self-inspections, driving continual improvement.\nServe as an additional Responsible Person on the WDA(H) licence, ensuring ongoing compliance with GDP and regulatory expectations.\nLead investigation, change control and CAPA activities, applying ICH Q9 Quality Risk Management principles.\nChampion GDP culture, deliver training, and promote quality awareness across the organisation.\nManage quality complaints and communication with the MAH and customers.\nMonitor KPIs, trends, and supplier performance to drive data-led improvement.About You:\n\nStrong background in pharmaceutical quality management, ideally within a WDA(H) environment.\nComprehensive knowledge of MHRA GDP and ISO9001.\nPrior Responsible Person (RP) experience (training can be provided).\nSkilled in inspection readiness, supplier qualification, risk management and continuous improvement.\nConfident communicator able to influence and promote quality culture across teams.Why Apply?\n\nThis is an exciting opportunity to join a stable, growing organisation with a strong reputation for quality and integrity. You'll be given autonomy, professional development, and the chance to make a real impact on compliance and operational excellence across a respected UK pharmaceutical business.\n\nTo apply or learn more, contact Gareth Gooley @ Smart4 Sciences - specialists in permanent recruitment across Quality and Regulatory Affairs within the life sciences sector
If you are interested in applying for this job please press the Apply Button and follow the application process. Energy Jobline wishes you the very best of luck in your next career move.
We focus on the Oil & Gas, Renewables, Engineering, Power, and Nuclear markets as well as emerging technologies in EV, Battery, and Fusion. We are committed to ensuring that we offer the most exciting career opportunities from around the world for our jobseekers.
Job Description
Quality Manager/Responsible Person - Pharmaceuticals - Gloucester\n\nSmart4 Sciences are proud to partner with an established and internationally recognised pharmaceutical company, renowned for their focus on the development, licensing and distribution of high-quality injectable medicines. With almost five decades of trusted service supplying the NHS, private healthcare, and global markets, they continue to lead in injectable and infusion therapies\n\nWe're now supporting them in hiring an experienced Quality Manager/Responsible Person (RP) to lead and continually improve the UK Quality Management System, uphold licence compliance, and embed GDP and ISO9001 best practice across their UK wholesale distribution operations.\n\nKey Responsibilities:\n\nManage and develop the UK Quality Management System (QMS) and eQMS, ensuring documentation, policies and procedures remain compliant and effective.\nMaintain WDA(H), GDP and ISO certifications; host regulatory inspections and manage responses through to closure.\nOversee internal audits, supplier audits and self-inspections, driving continual improvement.\nServe as an additional Responsible Person on the WDA(H) licence, ensuring ongoing compliance with GDP and regulatory expectations.\nLead investigation, change control and CAPA activities, applying ICH Q9 Quality Risk Management principles.\nChampion GDP culture, deliver training, and promote quality awareness across the organisation.\nManage quality complaints and communication with the MAH and customers.\nMonitor KPIs, trends, and supplier performance to drive data-led improvement.About You:\n\nStrong background in pharmaceutical quality management, ideally within a WDA(H) environment.\nComprehensive knowledge of MHRA GDP and ISO9001.\nPrior Responsible Person (RP) experience (training can be provided).\nSkilled in inspection readiness, supplier qualification, risk management and continuous improvement.\nConfident communicator able to influence and promote quality culture across teams.Why Apply?\n\nThis is an exciting opportunity to join a stable, growing organisation with a strong reputation for quality and integrity. You'll be given autonomy, professional development, and the chance to make a real impact on compliance and operational excellence across a respected UK pharmaceutical business.\n\nTo apply or learn more, contact Gareth Gooley @ Smart4 Sciences - specialists in permanent recruitment across Quality and Regulatory Affairs within the life sciences sector
If you are interested in applying for this job please press the Apply Button and follow the application process. Energy Jobline wishes you the very best of luck in your next career move.