Search scientific have been chosen to work with a panel of clients throughout the UK to assist in the process of recruiting for a regulatory affairs associate. As a regulatory affairs associate you will be responsible for compiling and submitting regulatory submissions for approval. You will also be responsible for maintaining technical files and design dossiers as well as being responsible for regulatory review and approval of key c...
Regulatory Affairs Associate, Agrochemical. Switzerland or UK. Salary based on experience. Leading global provider of essential non-clinical contract research and services to the chemical, agrochemical, pharmaceutical, biotech and medical device industries is seeking for a Regulatory Affairs Associate to join their growing Regulatory Affairs Department based in their laboratories in Shardlow, England or in Itingen, Switzerland. <br ...
Regulatory Affairs Associate, Chemical. Shardlow, UK. Salary based on experience. Leading global provider of essential non-clinical contract research and services to the chemical, agrochemical, pharmaceutical, biotech and medical device industries is seeking for a Regulatory Affairs Associate to join their Department of Registration Services based in their laboratories in Shardlow, England. Responsibilities include provi...
Regulatory Associate - Agrochemicals, Crop Protection, PPP Our client is a leading research organisation with an established history in offering high quality service and contribute in helping companies discover a solution to a certain medical need. For a quarter century they have offered consulting services to the Chemical/Agrochemical industry and now are the leading providers in training people within Regulatory. Therefore, you wil...
My client are a leading pharmaceutical company based in the East Midlands, they are currently looking for a Regulatory Affairs associate to join their well established team. The Role: You will be responsible for coordinating regulatory directives. You'll answer to governing bodies such as the MHRA on behalf of the company. You'll be responsible for both external and internal regulations in accord...
My client has a number of opportunities within their business from Regulatory Associate to Senior Affairs Associate and Manager. - Ideal candidates will have a Science Degree, at least 2-3 years experience within Regulatory Affairs, but not from clinical trials background. - Would also be preferred if you have a CMC or EU procedural experience for New Product submission. Purpose of these roles are to obtain and maintain ...
Job Description: Our client is seeking a Regulatory Affairs Associate II based in Berkshire Duties will include: Supports regulatory affairs and technical writing activities. Compiles and submits clinical trial applications and notifications to regulatory authorities and ethics committees. Ensures clinical trials are conducted such that subject's rights, safety and well being are protected and that the clinica...
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Date: 18 April
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Abingdon, Oxfordshire
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£30,000 - £40,000 per annum, negotiable, pro-rata, inc benefits
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4 applications
SENIOR RA ASSOCIATE - Medical Devices - Oxfordshire - Circa 35-40k Type: Permanent Reports to: RA Manager Purpose: Provide Regulatory and Quality Assurance support to the business. To operate as a member of the RA team with a mandate to promote a regulatory sound business practice and support the continuous improvement ethic throughout the organisation. Responsibilities: Reporting duties to RA ...
Regulatory Affairs Associate (REACh) £c23k North/Midlands AF/016458 A Regulatory Affairs Associate with experience in REACh and registration of chemicals is urgently required for a key service provider to the pharmaceutical, agrochemical and chemical, and government research organisations. Their focus is to optimise the discovery and safety of new medicines and compounds. The ...
Regulatory Affairs Associate (REACh) £c23k North/Midlands AF/016458 A Regulatory Affairs Associate with experience in REACh and registration of chemicals is urgently required for a key service provider to the pharmaceutical, agrochemical and chemical, and government research organisations. Their focus is to optimise the discovery and safety of new medicines and compounds. The r...
Regulatory Affairs Associate (REACh) £c23k North/Midlands AF/016458 A Regulatory Affairs Associate with experience in REACh and registration of chemicals is urgently required for a key service provider to the pharmaceutical, agrochemical and chemical, and government research organisations. Their focus is to optimise the discovery and safety of new medicines and compounds. The r...
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Date: 2 February 2010
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Dublin, Ireland
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€80,000 - €100,000 per annum
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19 applications
Ref: 45442 Location: Dublin North, Dublin West, Dublin City Centre Sal: Negotiable Edu: Degree Exp: 10 - 15 years Keywords: Regulatory Affairs Officer, Regulatory Affairs Co-ordinator, Regulatory Affairs Manager Associate Director of Regulatory Affairs My client is a provider of services and solutions to the pharmaceutical, medical devices, biopharmaceutical, healthcar...
6 jobs matching this search were posted in the last week
Organisation Description Reed Scientific are recruiting a Regulatory Affairs Associate to work for a growing and reputable Medical Device manufacturer in South Wales. Job Description Primary Work closely with process development teams to integrate Safety Assurance activities into product development processes. Construct Safety Assur...
Organisation Description Reed Scientific are recruiting a Regulatory Affairs Associate to work for a growing and reputable Medical Device manufacturer in South Wales. Job Description Primary Work closely with process development teams to integrate Safety Assurance activities into product development processes. Construct Safety Assur...
A leading provider of innovative medical technologies is looking to expand its North West based Clinical Affairs team, presenting an exciting opportunity for a Clinical Trials and Regulatory Associate. Based within their impressive site on the outskirts of Chester, the role is critical for the effective. Planning through to completion of clinical trials, and supports management of contract and finance Regulatory Affairs documentation and co...
Job Description: Our client is seeking a Senior Regulatory Affairs Associate based in Berkshire. - Compiles and submits clinical trial applications and notifications to regulatory authorities and ethics committees. - Ensures clinical trials are conducted such that subjects’ rights, safety and well being are protected and that the clinical trial data are reliable. - Provides regulatory affairs advice and support...
Job Description This position acts as the regional regulatory lead for assigned products and provides regulatory strategy and submission support to help drive the drug development process to bring innovative medicines to market. The job holder will be a key member of the regulatory sub-teams. The submission support could include the full spectrum of regulatory activities during the life cycle of a product, for example...
About Us From Huggies® diapers to Kleenex® facial tissues, Kimberly-Clark makes the essentials for a better life. Our 57,000 global employees are changing the world for the better with innovative products that create new categories and push existing ones to a higher level. While building our business, we’re also building careers through first-class education, engaging experiences and exposure to some of the world’s m...
About Us From Huggies® diapers to Kleenex® facial tissues, Kimberly-Clark makes the essentials for a better life. Our 57,000 global employees are changing the world for the better with innovative products that create new categories and push existing ones to a higher level. While building our business, we’re also building careers through first-class education, engaging experiences and exposure to some of the world’s m...
QLAB, based in Livingston, is a central laboratory where clinical trial samples collected from patients are sent for analysis. Our world-class laboratory provides full analytical support for a huge variety of analytical techniques. Our team of Project Service staff organize, set up and run these clinical trials both regionally and globally. They are involved in all aspects of trials working alongside Finance, Contracts, Regulatory Affairs,...
Regulatory Associate - (Ingredient Evaluation/ Risk Assessment /Toxicology) c22,800 + Bonus South East AF\016473 A regulatory executive is urgently required to provide regulatory support and ingredients evaluation within the Regulatory Affairs department across the R&D function of a global company. Working alongside a large team of regu...
Regulatory Associate - (Ingredient Evaluation/ Risk Assessment /Toxicology) c22,800 + Bonus South East AF\016473 A regulatory executive is urgently required to provide regulatory support and ingredients evaluation within the Regulatory Affairs department across the R&D function of a global company. Working alongside a large team of regul...
Regulatory Associate - (Ingredient Evaluation/ Risk Assessment /Toxicology) c22,800 + Bonus South East AF\016473 A regulatory executive is urgently required to provide regulatory support and ingredients evaluation within the Regulatory Affairs department across the R&D function of a global company. Working alongside a large team of regul...
