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📑 Responsibilities: The Pharmacovigilance & Regulatory Quality Assurance (PVRQA) Lead / PV Auditor is responsible for leading and coordinating the Global PVRQA activities in the respective region (Americas, Asia-Pacific (APAC), European Economic Area (EEA), ECI) under the general direction of the PVRQA Regional Head, to ensure th ...

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📑 Overview At Kyowa Kirin International (KKI), our purpose is to make people smile. This means more than drug discovery and development; it is about embedding care into everything we do to make a difference every day for those that need it most. We’re an inclusive pharmaceutical company that takes time to understand what really matters to our ...

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📑 We are looking to add a new critical reporting directly to the Executive Director of Global Patient Safety (GPS) within our Quality and Compliance Centers of Excellence (CoE). As the GPS Pharmacovigilance Intelligence Leader, you'll become a central figure in ensuring patient safety by navigating the evolving landscape of international pharmacovigi ...

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📑 Senior Manager Global Quality Operations (Senior PV Auditor)This is a home-based role offering a fantastic package including generous salary, incentive bonus, home based allowance plus much more. My client a Global pharmaceutical company are seeking an experienced Senior Manager, Global Quality Operations to manage and perform audits with focus on ...

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📑 Senior Manager Global Quality Operations (Senior PV Auditor)This is a home-based role offering a fantastic package including generous salary, incentive bonus, home based allowance plus much more. My client a Global pharmaceutical company are seeking an experienced Senior Manager, Global Quality Operations to manage and perform audits with focus on ...

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📑 Overview At Kyowa Kirin International (KKI), our purpose is to make people smile. This means more than drug discovery and development; it is about embedding care into everything we do to make a difference every day for those that need it most. We’re an inclusive pharmaceutical company that takes time to understand wha ...

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📑 Manager QA PV Auditor - 2406183539W **Description** At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promis ...

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📑 Brief Description: The Manager of Quality & Compliance (Q&C) for Pharmacovigilance (PV) is responsible for performing quality assurance activities to ensure that Jazz is adhering to Global applicable regulations, industry standards, Jazz policies, procedures and quality standards in support of the Quality Management System within the Researc ...

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📑 Why Patients Need You Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analy ...

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📑 Brief Description: The Manager of Quality & Compliance (Q&C) for Pharmacovigilance (PV) is responsible for performing quality assurance activities to ensure that Jazz is adhering to Global applicable regulations, industry standards, Jazz policies, procedures and quality standards in support of the Quality Management S ...

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📑 Brief Description: To lead Jazz’s Pharmacovigilance QA (GvP) function to assure regulatory compliance and data integrity in all Jazz activities related to Pharmacovigilance. Essential Functions In collaboration with the Sr Dir, Clinical & PV QA, ensures the implementation of the Global Quality strategy, as relevant to pharmacovigilance (P ...

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📑 Brief Description: To lead Jazz’s Pharmacovigilance QA (GvP) function to assure regulatory compliance and data integrity in all Jazz activities related to Pharmacovigilance. Essential Functions In collaboration with the Sr Dir, Clinical & PV QA, ensures the implementation of the Global Quali ...

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📑 Why Patients Need You Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, m ...

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📑 Brief Description: Prepare, perform, report and follow-up independent clinical quality assurance audits including associated quality management activities and provide input into the audit schedule. Acts as Lead auditor as applicable. To support Clinical Quality Assurance in its application and development of the Quality Management System and ...

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📑 We are looking to add a new critical reporting directly to the Executive Director of Global Patient Safety (GPS) within our Quality and Compliance Centers of Excellence (CoE). As the GPS Pharmacovigilance Intelligence Leader, you'll become a central figure in ensuring patient safety by navigating the evolving landscape of international pharmacovigi ...

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📑 We are looking to add a new critical reporting directly to the Executive Director of Global Patient Safety (GPS) within our Quality and Compliance Centers of Excellence (CoE). As the GPS Pharmacovigilance Intelligence Leader, you'll become a central figure in ensuring patient safety by navigating the evolving landscape of international pharmacovigi ...

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📑 We are looking to add a new critical reporting directly to the Executive Director of Global Patient Safety (GPS) within our Quality and Compliance Centers of Excellence (CoE). As the GPS Pharmacovigilance Intelligence Leader, you'll become a central figure in ensuring patient safety by navigating the evolving landscape of international pharmaco ...

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📑 The Manager, Global Aggregate Reports Quality and Compliance is an integral member of the Global Aggregate Report office and PV Writing Organization. The position holder responsibility includes the entire CSL product portfolio and development pipeline. Responsibilities include: - Acts as a Regulatory Intelligence Triage Manager, responsible for ...

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📑 Brief Description: Prepare, perform, report and follow-up independent clinical quality assurance audits including associated quality management activities and provide input into the audit schedule. Acts as Lead auditor as applicable. To support Clinical Quality Assurance in its application and development of the Qualit ...

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📑 The Manager, Global Aggregate Reports Quality and Compliance is an integral member of the Global Aggregate Report office and PV Writing Organization. The position holder responsibility includes the entire CSL product portfolio and development pipeline. Responsibilities include: - Acts as a Regulatory Intelligence Triage Manager ...

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📑 Job DescriptionReporting to Associate Director, Medical Safety Surveillance.Homebased role available in UK, Spain or US.Comprehensive salary, bonus and benefits package. Role overview:The Affiliate PV Partner Compliance Specialist supports the establishment and maintenance of effective compliance & oversight of external providers of pharmacovigilan ...

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📑 The GCSP Regions Head of Europe is a leadership position for providing end-to-end pharmacovigilance (PV) strategic insight and operational oversight for CSL enterprise affiliates and guiding PV operations in the Affiliates. The role directly manages personnel including Regions Territory Managers, and indirectly Safety Officers (SOs) in the regi ...

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📑 QA Specialist – Bio-pharmaceutical - Slough We are looking for an experienced QA Specialist for a fantastic 12 month contract based in Slough. Working with our client, a global bio-pharmaceutical organisation committed to improving the lives of people afflicted with neurological and immunological disease, you will b ...

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📑 Job Title: Quality Manager, Global Quality ManagementLocation: UK (preferably located near Windsor)Are you a Pharmacovigilance professional with a keen eye for quality management? Do you possess experience in audits, inspections, and CAPA management, and aspire to transition into a broader Quality role? We have an exciting opportunity for you to jo ...

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📑 Job Title: Quality Manager, Global Quality ManagementLocation: UK (preferably located near Windsor)Are you a Pharmacovigilance professional with a keen eye for quality management? Do you possess experience in audits, inspections, and CAPA management, and aspire to transition into a broader Quality role? We have an exciting opportunity for you to jo ...

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📑 **For Current Gilead Employees and Contractors:** Please log onto your Internal Career Site (~/cacheable-task/2997$2151.htmld#backheader=true) to apply for this job. At Gilead, we’re creating a healthier world for all people. For more ...

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📑 Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization ...

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📑 Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization ...

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📑 Description FUNCTION: Inflammation Therapeutic Area (TA) Global Safety Leader POSITION OVERVIEW: The ideal candidate will lead and champion the voice of patients in development programs. The candidate should be able to effectively strategize and implement benefit-risk activities across the product lifecycle. The candidate will also p ...

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📑 We are PrimeVigilance (part of Ergomed PLC), a specialized mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality A ...

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📑 We are PrimeVigilance (part of Ergomed PLC), a specialized mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality A ...

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📑 Job Title: Senior Regulatory Affairs & PV ManagerEmployment Type: Permanent positionLocation: East London, 3 days on-site. (Hybrid)Remuneration: Competitive salary and packageSenior Regulatory Affairs & PV Manager opportunity working for a growing pharmaceutical company specialising in medicinal, non-medicinal, medical devices, and OTC products. Th ...

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📑 Job Title: Senior Regulatory Affairs & PV ManagerEmployment Type: Permanent positionLocation: East London, 3 days on-site. (Hybrid)Remuneration: Competitive salary and packageSenior Regulatory Affairs & PV Manager opportunity working for a growing pharmaceutical company specialising in medicinal, non-medicinal, medical devices, and OTC products. Th ...

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📑 Our client, based in Dartford, were established in 2011. UK owned they are now expanding and are looking to recruit a Pharmacovigilance Co-ordinator.Job Description: * Develop and approve artwork components and patient information (SPC, PIL, cartons and labelling) and associated mock-ups. * Liaise with project managers for ...

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📑 Our client, based in Dartford, were established in 2011. UK owned they are now expanding and are looking to recruit a Pharmacovigilance Co-ordinator.Job Description: * Develop and approve artwork components and patient information (SPC, PIL, cartons and labelling) and associated mock-ups. * Liaise with project managers for ...

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📑 Description FUNCTION: Inflammation Therapeutic Area (TA) Global Safety Leader POSITION OVERVIEW: The ideal candidate will lead and champion the voice of patients in development programs. The candidate should be able to effectively strategize and implement benefit-risk activities acr ...

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📑 Role Overview We are currently looking for a Head of Regulatory Affairs and Pharmacovigilance to join a leading Pharmaceutical company based in the Kent area. As the Head of Regulatory Affairs and Pharmacovigilance you will be responsible for providing organisation with strategic advice for the launch of new products in EU & UK. Key Duti ...

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📑 My client specialises in the licensing and marketing cost-effective generic pharmaceuticals and is focused on growth through product launches and EU expansion. They want to increase their commercial foothold in the EU and expand their UK PV team.They are looking for a QPPV to ensure constant compliance with UK PV Legislation and UK Regulations and ...

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📑 My client specialises in the licensing and marketing cost-effective generic pharmaceuticals and is focused on growth through product launches and EU expansion. They want to increase their commercial foothold in the EU and expand their UK PV team.They are looking for a QPPV to ensure constant compliance with UK PV Legislation and UK Regulations and ...

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📑 Description FUNCTION: Medical Safety Science (MSS) / Global Therapeutic Area (TA) Safety Scientists POSITION OVERVIEW: You will develop or oversee and ensure that strategic scientific input relative to safety is incorporated into product development and lifecycle management as well a ...

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📑 Role Overview We are currently looking for a Head of Regulatory Affairs and Pharmacovigilance to join a leading Pharmaceutical company based in the Kent area. As the Head of Regulatory Affairs and Pharmacovigilance you will be responsible for providing organisation with strategic advice for the launch of new products in E ...

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📑 Job Description Job Title: Trainee Medical Device Lead Auditor Job Type: Permanent Hours: hours per week Job Location: Field-based (UK, South Region) Travel: Within the UK, a Company car or car allowance provided At SGS, we ...

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📑 Northreach is a dynamic recruitment agency that connects businesses with top talent in the Advanced therapy, fintech, and digital sectors. Our mission is to provide a seamless and personalised recruitment experience for clients and candidates, and to create a positive work environment that encourages equality, innovation, and professional growth.Jo ...

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📑 Northreach is a dynamic recruitment agency that connects businesses with top talent in the Advanced therapy, fintech, and digital sectors. Our mission is to provide a seamless and personalised recruitment experience for clients and candidates, and to create a positive work environment that encourages equality, innovation, and professional growth.Jo ...

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📑 About This Job : As we further build our Global Clinical development structure, we have a new opportunity for a Senior Director - Lead Clinical Development Scientist for Immuno- Oncology. The primary focus for this role is the management and input into the development of clinical strategies for assigned modalities or indications within the ...

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📑 About This Job : As we further build our Global Clinical development structure, we have a new opportunity for a Lead Clinical Development Scientist (Senior Director) for Oncology. The primary focus for this role is the management and input into the development of clinical strategies for assigned modalities or indications within the divisio ...

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📑 BioTalent is headhunting for a UK or Germany based Senior (Global) Drug Safety Physician who is fluent or business level professional in both English and French language. The role is remote with the option of office sites (in UK and Germany) to work from. Responsibilities: Lead clinical safety activities for assigned studies, ensuring compliance wi ...

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📑 BioTalent is headhunting for a UK or Germany based Senior (Global) Drug Safety Physician who is fluent or business level professional in both English and French language. The role is remote with the option of office sites (in UK and Germany) to work from. Responsibilities: Lead clinical safety activities for assigned studies, ensuring compliance wi ...

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📑 PV Systems Product Owner - PharmaceuticalsLocation: Paddington or Staffordshire Contract Type: PermanentSalary: £50,000 - £60,000 per annumOur client, an international organisation operating within the pharmaceutical industry, is seeking a PV Systems Product Owner to join their team. With a focus on providing bespoke end-to-end ...

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📑 PV Systems Product Owner - PharmaceuticalsLocation: Paddington or Staffordshire Contract Type: PermanentSalary: £50,000 - £60,000 per annumOur client, an international organisation operating within the pharmaceutical industry, is seeking a PV Systems Product Owner to join their team. With a focus on providing bespoke end-to-end ...

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