Regulatory Affairs Consultant Would you like to join a dynamic global Regulatory Affairs team and work on exciting projects? My client is looking for a new member of their Regulatory group. They are looking for an experienced pharmaceutical regulatory affairs professional who loves to manage projects Do you possess the following skills? - Pharmaceutical industry regulatory Affairs experience is an ab...
EU Dangerous Goods Safety Specialist / DGSA, Nottingham, Competitive package + Bens We are looking for a Dangerous Goods Safety Specialist / DGSA to join a global chemical business . Your role will be to ensure the business complies with Directives 2008/68/EC and 2000/18/EC to ensure that adequate / compliant processes for loading, unloading and transport of dangerous goods are in...
EU Dangerous Goods Safety Specialist / DGSA, Leicester, Competitive package + Bens We are looking for a Dangerous Goods Safety Specialist / DGSA to join a global chemical business . Your role will be to ensure the business complies with Directives 2008/68/EC and 2000/18/EC to ensure that adequate / compliant processes for loading, unloading and transport of dangerous goods are in ...
EU Dangerous Goods Safety Specialist / DGSA, Loughborough, Competitive package + Bens We are looking for a Dangerous Goods Safety Specialist / DGSA to join a global chemical business . Your role will be to ensure the business complies with Directives 2008/68/EC and 2000/18/EC to ensure that adequate / compliant processes for loading, unloading and transport of dangerous goods are ...
Organisation Description My client are a well respected multinational FMCG manufacturer, and they are looking for a Regulatory Affairs Manager for their fragrances side of the business. Job Description Job Description: 1. Managing materials of concern Regularly review portfolio of materials used with fragrances for potential updates t...
Our client is looking for someone to work within their regulatory team dealing with administration and secretarial duties Key skills required are: -Taking Minutes -Excellent IT skills - word, excel, adobe -Bookmarking in adobe, spreadsheets with formulas in excel, typing (speed and accuracy). -Editing documents. Previous experience within a project environment or technical environment this would be b...
Berkshire £60-80k dependant on experience, plus bonus and excellent benefits package My client is a large, well-established and rapidly growing pharmaceutical company specialising in the sales and marketing of proprietary brands and niche generic medicines. The company has been established for around 20 years and came in to existence though a joint venture between two large pharma manufacturers. They prov...
Do you have experience working in labeling? Are you looking for an exciting opportunity to join a global pharmaceutical company? This is an exciting opportunity to join a global pharmaceutical company working as a Labeling Document Specialist to support products in Research and Development. The main responsibility of the role will be converting labeling documents including core company data sheets and international packa...
Job Description To provide regulatory consultancy services to internal and external clients, including preparation, review, submission and project management of regulatory applications. Consultancy applicants are to act as a central point of contact for assigned key clients and work with other staff to promote and develop the business. Reed Specialist Recruitment Limited is an employment agency and emplo...
Job Description To provide regulatory consultancy services to internal and external clients, including preparation, review, submission and project management of regulatory applications. To act as the central point of contact for assigned key clients. To work with other staff to develop and promote the business. Reed Specialist Recruitment Limited is an employment agency and employment business ...
Our client is a leading pharmaceuticals business, due to rapid growth and expansion we are recruiting for an experienced Regulatory Affair Manager to join the team based in exclusive West London offices. As Regulatory Affairs Manager you will have previous experience and a deep understanding of National Phase procedures. Key responsibilities: Submission of End of Procedure national phase documents for C...
Experience in Pharmaceutical sector SMS experience a bonus Experience of artwork preparation process and organising appropriate processes People management Attention to detail is highly necessary due to nature of business Multi-tasking Batchelors Degree evel preferred in pharmacy or equivalent ...
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...
14 jobs matching this search were posted in the last week
Superb, brand new opportunity for a competent Regulatory and Quality Affairs Manager to join this rapidly growing, global radiotherapy equipment developer. As an experienced Regulatory and Quality Affairs Manager you will assist in extending the company’s expansion into new markets and territories. The Company: Our highly successful North London based client is a fast growing 3D imaging medical technology company speci...
EU Regulatory Labelling Officers, Permanent Based Herts/North London Based in Potters Bar, Herts (15 minutes from Kings Cross), Mylan has global revenues of $6.8 bn, a commercial presence in all EU and international regions and a robust, diverse portfolio of blockbuster products across all dosage forms. The substantial EU Regulatory Teams need support to manage the strategic compliance and generation of EU labelling content...
Regulatory CMC/Documentum Contractors-12 months Based Herts/North London Based in Potters Bar, Herts (15 minutes from Kings Cross), Mylan has global revenues of $6.8 billion, a commercial presence in all EU and international regions and a robust, diverse portfolio of blockbuster products across all dosage forms. The substantial EU Regulatory Teams in the UK need support to manage the strategic compliance and g...
Lab Solutions has an immediate need for a Regulatory Affairs Manager to join a global healthcare company.This role would entail day to day managing of the regulatory team, participating in new product introductions, ensuring products comply with national and European regulatory requirements, ensuring work is compliant with internal procedures.The candidate will have extensive experience managing/leading a team, high degree of technical comp...
Kelly.Diver@kellyservices My client are a leading pharmaceutical company based in West Yorkshire, they are currently seeking a Senior Regulatory Affairs specialist to join their well established team of accomplished scientists. The Role: To Prepare packaging, review against excipient guidelines, Check Packaged items. Braille check and conversant with EU Braille. Liasing with user te...
Job Description My client is looking for an experienced individual to be involved in a range of activities from the global authoring of compliant SDS to delivering regulatory consultancy on behalf of a diverse client base, while also participating or leading in project management and customer contact activities. In this role: The Regulatory Affairs Consultant will be responsible for managi...
Our client is a leading pharmaceuticals business, due to rapid growth and expansion we are recruiting for an experienced Regulatory Affair Manager to join the team based in exclusive West London offices. As Regulatory Affairs Manager you will have previous experience and a deep understanding of National Phase procedures. Key responsibilities: Submission of End of Procedure national phase documents for C...
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 ...
Environmental Risk Assessor, Newcastle-upon-Tyne, Exc Salary + bens We are looking for an Environmental Risk Assessor to join an expanding regulatory affairs and environmental risk assessment group. You will work on all aspects of risk assessment projects to help chemical, biocide and agchem companies register new products. Applications are invited from candidates with an MSc or PhD in an environmental chemistry or toxi...
Aquatic Ecotoxicologist, Suffolk, Negotiable salary + bens An excellent opportunity to join a large established state of the art aquatic ecotoxicology facility that offers a diverse range of indoor and outdoor studies for chemical, agrochemical and pharmaceutical compounds. As Study Director, you will manage and coordinate your own studies from start to finish. Ideally you will have existing aquatic ecotoxicology experience along...
My client is a small but highly successful manufacturing company with T/O of £3million. They work in Food, Industrial and Clinical markets. They are looking for a Technical Director specialising in Quality, Microbiology and R&D. The Role: Technical Director Within this role you would be responsible for quality and regulatory affairs management, and liaising with external bodies. Supporting R&D whi...
Pharmaceutical Head of Quality Management and Compliance - Croydon Opportunity : If you are looking for a new exciting opportunity or your next career change then this is a one off opportunity you do not want to miss out on. Your role as Head of Quality Management and Compliancebased in Croydon will involve leading and managing the quality and regulatory affairs departmentto achieve corporate complian...
