Our client is an API and intermediate manufacturer based in Hertfordshire. They are currently looking for a Regulatory Affairs Officer to join their regulatory department. Responsibilities: - You will assist in the compilation, assembly and submission of Drug Master Files and Certificate of Suitability for our clients existing and new Active Pharmaceutical Ingredients. - To assist in...
This well established family owned Japanese Pharmaceutical business in Slough, that has seen rapid growth over the past year to eighteen months, is seeking an experienced Regulatory Affairs officer to help take them forward to the next stage of their development. Roles and Responsibility - Liaising with MHRA (Medicines and Healthcare products Regulatory Agency) and EMEA. - Obtain information of regulatory a...
Your overall mission as Regulatory Affairs Officer within the healthcare / Pharma division of a global organisation is to support the business in the development of a range of pharmaceutical products for customers on a global basis. Looking for experience in the coordination of regulatory documentation including CTD and CEP documents to support new submission. Degree educated and a diploma in Regulatory Affairs would be advantageous. Full JD av...
Our Client is a Pharmaceutical Manufacturer. They are now seeking a Regulatory Affairs Officer . The position will be based in Hertfordshire and is a full-time permanent role. Responsibilities Assist in the completion, assembly and submission of Drug Master Files and Certificates of Suitability for existing and new Active Pharmaceutical Ingredients Working as part of a small team you will quickly be ...
Quality Assurance Officer - GLP, North Yorkshire, Competitive Salary + Bens An opportunity for a GLP Quality Assurance professional or, an Environmental Scientist with experience in a GLP environmental testing facility and a strong interest in auditing and QA. You will join an expanding quality assurance / QA team within a GLP regulated environmental testing and risk assessment group. Your role will be to work closely with...
Quality Assurance Officer - GLP, North Yorkshire, Competitive Salary + Bens An opportunity for a GLP Quality Assurance professional or, an Environmental Scientist with experience in a GLP environmental testing facility and a strong interest in auditing and QA. You will join an expanding quality assurance / QA team within a GLP regulated environmental testing and risk assessment group. Your role will be to work closely with...
QA Officer Pharmaceutical manufacturer based in Hertfordshire currently requires a 12 month Fixed Term QA Compliance Officer Specifics of the role include: Undertaking QA inspections of facilities and activities. Ensuring that procedures are complied with Undertaking internal quality audits Requesting, discussing and agreeing actions in response to a range of Quality events including deviat...
Amazing QARA Officer RA & QA Officer- ISO13485- Lancashire Regulatory Affairs (Tech Files) and Quality Assurance(ISO13485) Benefits: Upto30K - Starting Salary Pension Healthcare Annual Holidays SAYE Life Assurance x 4 Bonus Client: Based in the North West England my client is a small but a progressive Medical Device business. They owe their success enti...
Amazing QARA Officer RA & QA Officer- ISO13485- Lancashire Regulatory Affairs (Tech Files) and Quality Assurance(ISO13485) Benefits: Upto30K - Starting Salary Pension Healthcare Annual Holidays SAYE Life Assurance x 4 Bonus Client: Based in the North West England my client is a small but a progressive Medical Device business. They owe their success enti...
We have a number of opportunities available with a gene based biopharmaceutical company in Oxford who’s activities span research, clinical development, regulatory affairs and manufacturing. Vacancies exist for: Product Analysis and Release/Analytical Development Scientists Research Scientist - Vector Engineering Research Scientist - Cell Engineering (maternity cover) Biotechnologists Lab ...
We are working with a niche contract provider of regulatory, quality management and project management services to the pharmaceutical and medical device industries. The position will mainly be based at their head office, however the successful candidate should be expected to travel to client's sites as and when the need arises. We are looking for Regulatory Affairs Consultants with a range of knowledge in Regulatory Aff...
Our client are an established GMP pharmaceutical company who are looking for an experienced Regulatory Officer for a long term contract. Your position in this role who be focussed on providing regulatory support to marketed products for a range of products across the EU including inhalation, transdermal and conventional dosage forms. Responsibilities include: • Completion of renewals and associated follow up • Completion ...
Circa £30,000 per annum plus excellent benefits package Permanent - 35 hours per week Based in Houghton Regis, Nr Dunstable, Bedfordshire Certsure LLP is the joint venture between the Electrical Safety Council (ESC) and the Electrical Contractors’ Association (ECA) which acts as the sole certification and registration body for the NICEIC and ELECSA brands, serving over 36,000 electrical and Bu...
Amazing QARA Officer RA & QA Officer- ISO13485- Lancashire Regulatory Affairs (Tech Files) and Quality Assurance(ISO13485) Benefits: Upto30K - Starting Salary Pension Healthcare Annual Holidays SAYE Life Assurance x 4 Bonus Client: Based in the North West England my client is a small but a progressive Medical Device business. They owe their success enti...
Permanent Headcount East Midlands (may be option for partially home-based or part time) Our client is a rapidly growing global specialty pharmaceutical company focused on the development, in and out-licensing and marketing of innovative gastroenterology products. They are a very passionate company who treat their employees with fairness and respect, rewarding excellent performance, honesty and entrepreneurship. ...
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Date: 2 February 2010
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Galway, Ireland
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€100,000 - €120,000 per annum
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18 applications
ob Ref: 43873 Location: Offaly, Westmeath, Laois Sal: Negotiable Edu: Degree Exp: 7+ year Keywords: Regulatory Affairs Manager, Regulatory Affairs Specialist, Regulatory Affairs Officer DESCRIPTION: Director of Regulatory Affairs Applications are invited for the permanent opportunity of Director, Regulatory Affairs based in Athlone. The role will be respons...
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Date: 12 June 2009
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Dublin, Ireland
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€120,000 - €160,000 per annum
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19 applications
Job Ref: 44597 Location: Westmeath, Dublin City Centre, Nationwide Edu: Degree Exp: 10 + year Keywords: Regulatory Affairs Manager, Regulatory Affairs Specialist, Regulatory Affairs Officer DESCRIPTION: VP of Global Regulatory Affairs Applications are invited for the permanent opportunity of VP of Global Regualtory Affairs. The role will be responsible for ensuri...
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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...
Sental Recruitment are currently seeking an experienced regulatory affairs officer for our global client. The role offers a fantastic salary of 35- 40K plus excellent benefits. This is a truly fantastic company to work for. Experience required in the following: Product licensing/dossier completion Pharma or medical device Providing regulatory strategy Global registration labelling ...
Reporting to the Product Development Manager, this post controls all technical documentation activities relating to formulated products and purchased or customer supplied raw materials. You will ensure that all new products comply with relevant regulations and internal policies, can be legally sold in all markets, solve registration problems in existing markets, maintain product files and ensure regulatory approval of all NPD formula...
