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📑 We are currently seeking a talented and experienced Regulatory Affairs Project Manager to join our client's team in Surrey. Our client is an established cosmetics/pharmaceuticals company looking for someone with expertise in global cosmetic regulations. In collaboration with a highly skilled international team you will support in the pr ...

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📑 Title : Senior Medical Science Liaison Territory : Southwestern US An evolving international research focused pharmaceutical company dedicated to the advancement and advocacy of products tailored for the hospital, related specialty, and rare disease sectors is seeking a highly motivated and well experienced Senio ...

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📑 We are currently seeking a talented and experienced Senior Regulatory Affairs Manager to join our client's team in Surrey. Our client is an established cosmetics/pharmaceuticals company looking for someone with expertise in global cosmetic regulations. In collaboration with a highly skilled international team you will help to manage the ...

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📑 The Operations Systems Engineering team provide software and hardware integrated solutions to support the manufacture and testing. Working with teams across Quality Assurance, Operations, Technical Investigation and R&D and the product software design and Third Party Manufacturing groups, the Systems team deliver best in class systems solutions wit ...

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📑 Responsibilities:• Conduct Human Factors studies to assess the usability of medical devices, including designing and implementing formative and summative studies, as well as managing project plans and third-party support.• Conducting research (interviewing study participants and gathering data). • Conducting quality checks on study data and analysi ...

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📑 Responsibilities:• Conduct Human Factors studies to assess the usability of medical devices, including designing and implementing formative and summative studies, as well as managing project plans and third-party support.• Conducting research (interviewing study participants and gathering data). • Conducting quality checks on study data and analysi ...

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📑 The Operations Systems Engineering team provide software and hardware integrated solutions to support the manufacture and testing. Working with teams across Quality Assurance, Operations, Technical Investigation and R&D and the product software design and Third Party Manufacturing groups, the Systems team deliver best in class systems solutions wit ...

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📑 Position OverviewConsolidations, Planning, and Essbase professional with direct responsibility of managing and maintaining the Oracle EPM platform, which includes FCCS, EPBCS and Essbase applications. You will also be responsible to liaise between business teams and IT.What You'll DoMaintenance, administration and development of EPM applications, i ...

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📑 Position OverviewConsolidations, Planning, and Essbase professional with direct responsibility of managing and maintaining the Oracle EPM platform, which includes FCCS, EPBCS and Essbase applications. You will also be responsible to liaise between business teams and IT.What You'll DoMaintenance, administration and development of EPM applications, i ...

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📑 SailPoint is the leader in identity security for the cloud enterprise. Our identity security solutions secure and enable thousands of companies worldwide, giving our customers unmatched visibility into the entirety of their digital workforce, ensuring workers have the right access to do their job – no more, no less. Built on a foundatio ...

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📑 Oracle EPM Architect Are you an Oracle EPM Architect who is passionate about selling and delivering innovative EPM solutions? This is a fantastic opportunity to work with a Big 4 firm who have the internal Partner networks to bring unlimited warm opportunity to their EPM Practice. Our client’s capability has multiple in-flight Programmes and a rich ...

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📑 Oracle EPM Architect Are you an Oracle EPM Architect who is passionate about selling and delivering innovative EPM solutions? This is a fantastic opportunity to work with a Big 4 firm who have the internal Partner networks to bring unlimited warm opportunity to their EPM Practice. Our client’s capability has multiple in-flight Programmes and a rich ...

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📑 About SailPoint: SailPoint is the leader in identity security for the cloud enterprise. Our identity security solutions secure and enable thousands of companies worldwide, giving our customers unmatched visibility into the entirety of their digital workforce, ensuring workers have the right access to do their job – no more, no ...

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📑 Oracle EPM Senior Consultant - Planning / PCMOracle EPM Senior Consultant urgently required by a rapidly expanding global boutique consultancy.This role will see you work on a major Government project and therefore ideally requires someone who holds SC level Security Clearance (or someone who is clearable).You must have experience of Planning and P ...

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📑 Oracle EPM Senior Consultant - Planning / PCMOracle EPM Senior Consultant urgently required by a rapidly expanding global boutique consultancy.This role will see you work on a major Government project and therefore ideally requires someone who holds SC level Security Clearance (or someone who is clearable).You must have experience of Planning and P ...

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📑 Oracle EPM Senior Consultant Oracle EPM Senior Consultant required by a rapidly expanding global boutique consultancy.Do you have experience in Oracle EPM? Are you skilled in one or more of Planning, PCM, Consolidation, OneStream or Tax? Joining a team of EPM experts who are working with the Oracle EPM cloud suite, this is a fantastic opportunity t ...

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📑 Oracle EPM Senior Consultant Oracle EPM Senior Consultant required by a rapidly expanding global boutique consultancy.Do you have experience in Oracle EPM? Are you skilled in one or more of Planning, PCM, Consolidation, OneStream or Tax? Joining a team of EPM experts who are working with the Oracle EPM cloud suite, this is a fantastic opportunity t ...

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📑 Senior Scientist - Analytical Development Location: Coventry, RI Working situation: On-site Level: Senior Scientist Our client, a well-known pharmaceuticals firm, is working to produce innovative drug therapies with multiple products in pipeline from pre-clinical to the ...

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📑 Key Responsibilities: Documentation: Draft and revise procedures to meet regulations, cGMPs, and internal policies. Quality Standards: Apply and maintain quality standards and procedures for quality systems. cGMP Documentation: Review cGMP documents and lead or participat ...

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📑 Senior Compliance Auditor Role Description: Oversee and participate in audits, reporting on findings. Manage Quality Technical Agreements with critical suppliers. Conduct internal audits to meet GMPs, 820 standards, and company requirements. Lead and support supplier audits (onsit ...

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📑 Job Responsibilities : Lead and develop a team of Quality Assurance Specialists. Oversee final product release and adherence to cGMP regulations. Conduct inspections, review deviations, and manage corrective actions. Provide training and mentorship to team members. Collaborate ef ...

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📑 Title: Senior Clinical Project ManagerSalary: Highly CompetitiveLocation: Surrey area (Hybrid)If you have a clinical background and are interested in joining an exciting international organisation then this could be the role for you!This company is a leading biotech with products on the market. They are a well funded organisation that is continuous ...

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📑 The Director, Global Regulatory Affairs will be responsible for developing, implementing, and advising on global regulatory strategies for development programs to secure and maintain market access for product(s) in line with business objectives.DESCRIPTION OF THE ROLE• Provide high level strategic and operational regulatory direction and mentorship ...

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📑 Regulatory Affairs AssociateThe Regulatory Affairs Associate will be responsible for:• Managing the clinical trial applications in Europe and other selected countries • Keeping up to date with regulatory and legal changes in EU• Preparing pre- and post-authorisation regulatory documentation and applications • Assisting in marketing access activitie ...

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📑 Title: Senior Clinical Project ManagerSalary: Highly CompetitiveLocation: Surrey area (Hybrid)If you have a clinical background and are interested in joining an exciting international organisation then this could be the role for you!This company is a leading biotech with products on the market. They are a well funded organisation that is continuous ...

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📑 Title: Senior Medical Director of Clinical Development & Medical Affairs Location: New Jersey, USA OR Remote (Continental USA only) A mid-size pharmaceutical company is hiring a Senior Medical Director to join the Global Clinical Development and Medical Affairs team. As Senior Medical Director, you will have oversight of a multi-disciplinary ...

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📑 Senior Compliance Auditor Role Description: Oversee and participate in audits, reporting on findings. Manage Quality Technical Agreements with critical suppliers. Conduct internal audits to meet GMPs, 820 standards, and company requirements. Lead and support supplier audits (onsite and remote) for GMP and regulatory compliance. Uphold th ...

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📑 Senior Global Market Access Manager Wanted for Leading Pharmaceuticals CompanyWe are currently seeking an experienced and highly skilled Senior Global Market Access Manager to join our client's team in London, UK. Our client is a leading pharmaceuticals company that specializes in developing innovative treatments for patients worldwide.Responsibili ...

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📑 Senior Global Market Access Manager Wanted for Leading Pharmaceuticals CompanyWe are currently seeking an experienced and highly skilled Senior Global Market Access Manager to join our client's team in London, UK. Our client is a leading pharmaceuticals company that specializes in developing innovative treatments for patients worldwide.Responsibili ...

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📑 Key Responsibilities: Develop product strategies aligned with business objectives Conduct market research and analysis to identify customer needs and trends Collaborate cross-functionally with R&D, marketing, sales teams etc. Manage entire product lifecycle from ideation through launch till end-of-life management Qualifications: B ...

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📑 Job Title: Sales Specialist Company Type: Small Biotech Territory: Birmingham, AL Therapy Area: Rare Disease / Endocrinology Why This Role: Visibility- Join a growing small biotech Stability - Strong pipeline across Oncology, Endocrinology, and Neuro ...

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📑 Regulatory Affairs AssociateThe Regulatory Affairs Associate will be responsible for:• Managing the clinical trial applications in Europe and other selected countries • Keeping up to date with regulatory and legal changes in EU• Preparing pre- and post-authorisation regulatory documentation and applications • Assisting in marketing access activitie ...

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📑 Key Responsibilities: Develop product strategies aligned with business objectives Conduct market research and analysis to identify customer needs and trends Collaborate cross-functionally with R&D, marketing, sales teams etc. Manage entire product lifecycle from ideation throu ...

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