📑 Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you! The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and s ...
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📑 Supply Chain Quality Associate - Maidenhead, England - PermanentProclinical is seeking a dedicated QA Associate for our Supply Chain Quality Assurance team. This is a permanent position located in Maidenhead, England.Primary Responsibilities:The primary focus of this role is to work with internal and external stakeholders to ensure the timely relea ...
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📑 Supply Chain Quality Associate - Maidenhead, England - Permanent Proclinical is seeking a dedicated QA Associate for our Supply Chain Quality Assurance team. This is a permanent position located in Maidenhead, England. Primary Responsibilities: The primary focus of this role is to work with internal and external stakeholders to ensure th ...
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📑 Supply Chain Quality Associate - Maidenhead, England - PermanentProclinical is seeking a dedicated QA Associate for our Supply Chain Quality Assurance team. This is a permanent position located in Maidenhead, England.Primary Responsibilities:The primary focus of this role is to work with internal and external stakeholders to ensure the timely relea ...
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📑 Supply Chain Quality Associate - Maidenhead, England - Permanent Proclinical is seeking a dedicated QA Associate for our Supply Chain Quality Assurance team. This is a permanent position located in Maidenhead, England. Primary Responsibilities: The primary focus of this role is to work with in ...
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📑 SUMMARYThe QHSE Associate/Professional is responsible for reviewing and verifying the Safety and Health Policies, Procedures, Plans and training requirements on behalf of AVETTA Operators and Contractor Members. They help maintain the ISO9001 Quality Management System, Avetta’s SSIP Membership and ISO17020 UKAS Accreditation. The QHSE Associate/Pro ...
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📑 Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you! The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and s ...
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📑 SUMMARYThe QHSE Associate/Professional is responsible for reviewing and verifying the Safety and Health Policies, Procedures, Plans and training requirements on behalf of AVETTA Operators and Contractor Members. They help maintain the ISO9001 Quality Management System, Avetta’s SSIP Membership and ISO17020 UKAS Accreditation. The Q ...
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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,0 ...
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📑 SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote. The Role: The Regulatory Associate is responsible for providing global regulatory expe ...
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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 1 ...
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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,00 ...
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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,00 ...
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📑 Working within the Global Marine and Navy business unit you will provide technical writing support to JCI and our customers. Client portfolio will cover UK and international navies but also commercial vessels such as cargo ships, tankers, ferries, and yachts. The role will involve developing technical documentation across several contracts. The ...
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📑 AVK is a leading player in the energy sector, committed to driving innovation and sustainability in critical power installations. We are on a mission to transform the industry, aligning our strategies with a sustainable future.We are seeking an Administrator with Document Control experience to join our busy Engineering team at Head Office ...
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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 1 ...
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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,0 ...
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📑 We’re currently recruiting for a Regulatory Clinical Trial Strategy & Submissions Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead/hybrid.The Role:Deliver CTA regulatory strategies and operations for a designated port ...
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📑 We’re currently recruiting for a Regulatory Clinical Trial Strategy & Submissions Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead/hybrid.The Role:Deliver CTA regulatory strategies and operations for a designated port ...
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📑 This well-known firm is looking to expand their Employment team in Maidenhead with a 4+ years PQE Solicitor who shares their passion for client care to join at either the Associate or Senior associate level. The firm: This firm has built-up an excellent reputation and have set themselves apart from their competitors as the 'go to' firm for ...
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📑 This position is responsible for working with internal and external stakeholders to ensure timely release of finished product and high standards of compliance for transportation, storage and commercial distribution. Provide Quality support to the commercial affiliates and oversight of in-country distribution and Global Logistics providers includin ...
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📑 This well-known firm is looking to expand their Employment team in Maidenhead with a 4+ years PQE Solicitor who shares their passion for client care to join at either the Associate or Senior associate level. The firm: This firm has built-up an excellent reputation and have set themselves apart from their ...
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📑 Role: Regulatory Affairs Associate Location: Maidenhead / M4 corridor. Salary: Very competitive salary on offerPlanet Pharma are supporting a leading large global pharma company with the search for a new Regulatory Affairs Associate to join them during an exciting period of growth! Perfect for a junior regulatory professional with 6-24 months regul ...
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📑 Role: Regulatory Affairs Associate Location: Maidenhead / M4 corridor. Salary: Very competitive salary on offerPlanet Pharma are supporting a leading large global pharma company with the search for a new Regulatory Affairs Associate to join them during an exciting period of growth! Perfect for a junior regulatory professional with 6-24 months regul ...
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📑 Estate Agent | Lister/Valuer | Premium Homes Fine & Country Marlow & Maidenhead Are you an experienced Estate Agent, Manager, Lister or Valuer? Fine & Country have an immediate opening for an Associate to work the premium housing market in Marlow & Maidenhead. What you do:</ ...
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📑 This position is responsible for working with internal and external stakeholders to ensure timely release of finished product and high standards of compliance for transportation, storage and commercial distribution. Provide Quality support to the commercial affiliates and oversight of in-country distribution and Global Logistics providers inclu ...
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📑 A Qualified (ACA,ACCA,CIMA) Finance Manager is required to join an exceptional company based in Maidenhead on a permanent basis. We are excited to be partnering with a fun, vibrant and diverse business who are continually striving to develop their staff and business.They are based in very modern offices in Maidenhead and offer hybrid working, 3 day ...
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📑 Corporate Support Specialist EMEA - SalesOur client is a world renowned American software company that empowers creatives and businesses worldwide with a diverse range of innovative digital tools and solutions aimed at enhancing productivity, creativity, and digital experiences across various industries and they have an immediate requirement for a ...
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📑 Corporate Support Specialist EMEA - SalesOur client is a world renowned American software company that empowers creatives and businesses worldwide with a diverse range of innovative digital tools and solutions aimed at enhancing productivity, creativity, and digital experiences across various industries and they have an immediate requirement for a ...
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📑 Description Role purposeDefine, architect, design, develop, document and test complex FPGA firmware functions and algorithms within the Cyber UK Business Unit.ScopeDefine, architect, design, develop, document and test FPGA firmware as part of our 20 strong firmware engineering team, with ...
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📑 Description Hybrid working options available.As Quality Engineer working within Ultra Cyber and based in our brand new Maidenhead facility, you will develop and implement project quality plans in line with Cyber and customer’s specifications/requirements whilst ensuring that defined quality object ...
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📑 Corporate Sales Associate, EMEALocation: Maidenhead office (hybrid role with minimum 1-2 days per week onsite)Contract Length: 12 months with potential for extensionYou’ll provide essential administrative and coordination support to the Director of Corporate Sales. Your role will be instrumental in executing their corporate sales strategy and ensur ...
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📑 Corporate Sales Associate, EMEALocation: Maidenhead office (hybrid role with minimum 1-2 days per week onsite)Contract Length: 12 months with potential for extensionYou’ll provide essential administrative and coordination support to the Director of Corporate Sales. Your role will be instrumental in executing their corporate sales strategy and ensur ...
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📑 SRG are currently looking for a Payroll Manager for a Global Pharmaceutical Company who have opened a new vacancy within their team on an initial 6 Month basis to be based at their offices in either Maidenhead or Liverpool. Hybrid role with 1-2 days in the office. The Role:Overall responsibility for payroll processing for large volu ...
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📑 A Qualified (ACA,ACCA,CIMA) Finance Manager is required to join an exceptional company based in Maidenhead on a permanent basis. We are excited to be partnering with a fun, vibrant and diverse business who are continually striving to develop their staff and business.They are based in very modern offices in Maidenhead and offer hybrid working, 3 day ...
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📑 A Qualified (ACA,ACCA,CIMA) Finance Manager is required to join an exceptional company based in Maidenhead on a permanent basis. We are excited to be partnering with a fun, vibrant and diverse business who are continually striving to develop their staff and business.They are based in very modern offices in Maidenhead and offer hybrid working, 3 day ...
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📑 A Qualified (ACA,ACCA,CIMA) Finance Manager is required to join an exceptional company based in Maidenhead on a permanent basis. We are excited to be partnering with a fun, vibrant and diverse business who are continually striving to develop their staff and business.They are based in very modern offices in Maidenhead and offer hybrid ...
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📑 **About Abbott** Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. **Working at Abbott** At Abbott, you can do work that matters, grow, and learn, care for yourself and family, b ...
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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 1 ...
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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 1 ...
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📑 With over 90 years’ combined experience of delivering workforce solutions to the global energy industry, NES Fircroft is proud to be the world’s leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Infrastructure, Life Sciences, Mining, Automotive and Chemicals sectors worldwide.We provide tailored staffing solutions, s ...
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📑 A market leading company based in Maidenhead are looking for a Senior Credit Underwriter Analyst to join their growing team. This is a fantastic experience for someone with 2 years plus experience in Credit Control. The company has an amazing culture with fantastic offices, excellent benefits and incentives.Responsibilities:Report d ...
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📑 A market leading company based in Maidenhead are looking for a Senior Credit Underwriter Analyst to join their growing team. This is a fantastic experience for someone with 2 years plus experience in Credit Control. The company has an amazing culture with fantastic offices, excellent benefits and incentives.Responsibilities:Report d ...
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📑 A market leading company based in Maidenhead are looking for a Senior Credit Underwriter Analyst to join their growing team. This is a fantastic experience for someone with 2 years plus experience in Credit Control. The company has an amazing culture with fantastic offices, excellent benefits and incentives.Responsibilities:Report d ...
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📑 Our client is a leading manufacturer, supplier and installers of high-end acoustic blinds, curtains and window shadings into commercial construction and refurbishment projects.They have an exciting career opportunity for a Project Coordinator to join the business on a permanent basis. The core of this role will be to support the project manager ...
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📑 Our client is a leading manufacturer, supplier and installers of high-end acoustic blinds, curtains and window shadings into commercial construction and refurbishment projects.They have an exciting career opportunity for a Project Coordinator to join the business on a permanent basis. The core of this role will be to support the project manager ...
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📑 A Qualified (ACA,ACCA,CIMA) Finance Manager is required to join an exceptional company based in Maidenhead on a permanent basis. We are excited to be partnering with a fun, vibrant and diverse business who are continually striving to develop their staff and business.They are based in very modern offices in Maidenhead and offer hybrid work ...
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📑 A Qualified (ACA,ACCA,CIMA) Finance Manager is required to join an exceptional company based in Maidenhead on a permanent basis. We are excited to be partnering with a fun, vibrant and diverse business who are continually striving to develop their staff and business.They are based in very modern offices in Maidenhead and offer hybrid work ...
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📑 Role: Regulatory Affairs AssociateLocation: Maidenhead / M4 corridor.Salary: Very competitive salary on offerPlanet Pharma are supporting a leading large global pharma company with the search for a new Regulatory Affairs Associate to join them during an exciting period of growth! Perfect for a junior regulatory professional with 6-24 months regulat ...
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📑 Role: Regulatory Affairs AssociateLocation: Maidenhead / M4 corridor.Salary: Very competitive salary on offerPlanet Pharma are supporting a leading large global pharma company with the search for a new Regulatory Affairs Associate to join them during an exciting period of growth! Perfect for a junior regulatory professional with 6-24 months regulat ...
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Great News! We have discovered exciting live Associate quality document manager job opportunities in Maidenhead just for you at United Kingdom Jobs Expertini. You can even download the search results for Associate quality document manager jobs in maidenhead here.
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There are currently 1040 live jobs available for Associate quality document manager in Maidenhead according to United Kingdom Jobs Expertini.
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The average salary range for your role varies, but the standard pay scale is rated "Standard" for Maidenhead within United Kingdom. As said, salary levels may vary depending on your industry, experience, and skills, so it's essential to research and negotiate effectively.
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