📑 Overview Job Title: Regulatory Affairs Manager (Food & Beverages) Job Type: Permanent position Location: Chiswick, Cambridge, or Manchester – 2 days on-site per week. Remuneration: £50,000 – £55,000 + benefits This is an excellent opportunity to join a family-owned, Japanese business started in 1804, which is the number one sus ...
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📑 Job description Cyber Response & Recovery – Manager - 103539 Base Location: London/Manchester plus network of 20 offices nationally: The KPMG Risk Consulting function is a cornerstone of our business. Operating from locations across the UK we do work that matters, serving the country with diligence and expertise. KPMG is one of ...
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📑 Cambridge Environmental Assessments (CEA) is looking for a Regulatory Ecotoxicologist on a full-time or part-time, permanent basis. We are based in Boxworth, Cambridge however as the business has offices throughout the UK, we are happy to consider hybrid or fully remote working, depending on candidate preference. As the Ecotoxicologist, you will jo ...
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📑 Cambridge Environmental Assessments (CEA) is looking for a Regulatory Ecotoxicologist on a full-time or part-time, permanent basis. We are based in Boxworth, Cambridge however as the business has offices throughout the UK, we are happy to consider hybrid or ful ...
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📑 Job description Job Title/Req Number: Procurement Transformation Lead / Training Facilitator (103652) Base Location: London, Manchester or Bristol plus network of 20 offices nationally: The KPMG Infrastructure, Government and Healthcare – Procurement Operational Transformation practice (IGH-POT) function is a cornerstone of our busi ...
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📑 Are you interested in working on innovative projects such as Erebus, Salamander and Dolphyn? ERM is a leading consultancy in consenting floating offshore wind projects and we need your skills! We are seeking a Senior to Principal EIA Consultant (depending on experience) in offshore wind. Experience of consenting Scottish offshore wind projects ...
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📑 Are you interested in working on innovative projects such as Erebus, Salamander and Dolphyn? ERM is a leading consultancy in consenting floating offshore wind projects and we need your skills! We are seeking a Senior to Principal EIA Consultant (depending on experience) in offshore wind. Experience of consenting Scottish offsh ...
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📑 Job description Job Title/Req Number: Procurement Transformation Lead / Training Facilitator (103652) Base Location: London, Manchester or Bristol plus network of 20 offices nationally: The KPMG Infrastructure, Government and Healthcare – Procurement Operational Transform ...
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📑 Regulatory Affairs Specialist - Fully RemoteThis is an excellent Regulatory Affairs Specialist / RA Specialist, working for a company with a growing reputation in their field. The successful Regulatory Affairs Specialist / RA Specialist will have hands-on knowledge of FDA regulations, ISO standards & SaMD - as well as proven experience working with ...
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📑 Regulatory Affairs Specialist - Fully RemoteThis is an excellent Regulatory Affairs Specialist / RA Specialist, working for a company with a growing reputation in their field. The successful Regulatory Affairs Specialist / RA Specialist will have hands-on knowledge of FDA regulations, ISO standards & SaMD - as well as proven experience working with ...
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📑 The Opportunity: We are looking for a strategic regulatory leader to join our growing regulatory team at Relay Tx. You will have the opportunity to help define and implement innovative regulatory strategies to expedite the development and approval of our transformative pipeline. You will serve as the regulatory representative on relevant proje ...
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📑 The Opportunity: We are looking for a strategic regulatory leader to join our growing regulatory team at Relay Tx. You will have the opportunity to define and implement innovative regulatory strategies to expedite the development and approval of our transformative pipeline. You will serve as the global regulatory lead on relevant project teams ...
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📑 The Opportunity: We are looking for a strategic regulatory leader to join our growing regulatory team at Relay Tx. You will have the opportunity to define and implement innovative regulatory strategies to expedite the development and approval of our transformative pipeline. You will serve as the global regulatory lead on relev ...
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📑 My client is a global biopharma company. They are seeking a Regulatory Affairs Manager (CMC) to join our Regulatory Affairs Team based in Cambridge on a 12 month contract. Hybrid working Key Responsibilities Co-ordinate the preparation of high quality CMC documents to support regulatory submissions in International regions, (Asia, Latin Amer ...
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📑 My client is a global biopharma company. They are seeking a Regulatory Affairs Manager (CMC) to join our Regulatory Affairs Team based in Cambridge on a 12 month contract. Hybrid working Key Responsibilities Co-ordinate the preparation of high quality CMC documents to support regulatory submissions in International r ...
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📑 Description We are looking for a driven individual who is passionate about bringing transformational medicines to those in Europe and international countries with continued unmet medical need. This is an exciting opportunity for a Regulatory Affairs Associate Director to join the Gilead Global Regulatory Affairs Oncology team to suppor ...
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📑 Description We are looking for a driven individual who is passionate about bringing transformational medicines to those in Europe and international countries with continued unmet medical need. This is an exciting opportunity for a Regulatory Affairs Associate Director to join the Gilead Global Regulatory Affairs Oncology team to suppor ...
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📑 Location: Cambridge (Hybrid working - On average two or three times a month in the office) Job type: Permanent At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees. < ...
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📑 Location: Cambridge (Hybrid working - On average two or three times a month in the office) Job type: Permanent At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, ...
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📑 Job PurposeThe Manager, Medical & Regulatory Writing will be an integral part of MoonLake’s Clinical Development team. You will lead the development of content for submissions to regulatory agencies and other external stakeholders.This role will partner closely with key internal and external stakeho ...
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📑 About the job In the context of our growing activities, we are looking for a Regulatory Affairs Specialist to join our teams in the United Kingdom. You will integrate a team of dedicated Regulatory Affairs professionals and will have the mission to develop PLG’s local UK Regulatory Affairs presence, taking res ...
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📑 Location: Cambridge (Hybrid working - On average two or three times a month in the office) Job type: Permanent At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees. < ...
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📑 Location: Cambridge (Hybrid working - On average two or three times a month in the office) Job type: Permanent At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees. The Global Regulator ...
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📑 Job Description At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s bigg ...
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📑 Job PurposeThe Manager, Medical & Regulatory Writing will be an integral part of MoonLake’s Clinical Development team. You will lead the development of content for submissions to regulatory agencies and other external stakeholders.This role will partner closely with key internal and external stakeholders and requires critical thinking along with e ...
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📑 Description Regulatory Affairs Associate Director Gilead Sciences, Inc. is a research-based biopharmaceutical company founded in 1987, that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. Together we deliver life-saving therapies to patients in n ...
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📑 About the job In the context of our growing activities, we are looking for a Regulatory Affairs Specialist to join our teams in the United Kingdom. You will integrate a team of dedicated Regulatory Affairs professionals and will have the mission to develop PLG’s local UK Regulatory Affairs presence, taking responsibility for new regulatory ...
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📑 Description We are looking for a driven individual who is passionate about bringing transformational medicines to those in Europe and international countries with continued unmet medical need. This is an exciting opportunity for a Regulatory Affairs Associate Director to join the Gilead Glob ...
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📑 Job PurposeAs a Senior Manager, Regulatory Affairs CMC, you are an integral part of MoonLake’s Clinical Development team responsible for the development, execution and tracking of regulatory CMC and medical device activities.You will be responsible for the development of a CMC and device regulatory strategy, working closely with Technical Operation ...
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📑 About the job To strengthen our regulatory affairs division in the UK and Europe, RNI (a ProductLife Group Company) is urgently looking for a Regulatory Affairs Consultant with experience working on nutrition & health products in the UK and Europe. About us Group 10 Responsibilities The candidate will have 7+ years’ experience i ...
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📑 Job Description At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s bigg ...
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📑 Regulatory Affairs Labelling Associate Project Manager contract job Your newpany This well-known biopharmaceuticalpany is looking for a Regulatory Affairs Labelling Associate Project Manager to join their Labelling team on a contracting basis. This is a 12-month contract job with scope for extension and is fully remote. Your new role As part of t ...
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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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Great News! We have discovered exciting live Regulatory manchester job opportunities in Cambridge just for you at UK Jobs. You can even download the search results for Regulatory manchester jobs in cambridge here.
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