6-12 Months- REACH Registration Specialist- Chemicals- IUCLID, SIEFs + Product Stewardship. Based in the West Midlands our client is a renowned chemical solutions business seeing a surge in the demand and growth simultaneously. To ensure that REACH Registration projects of customers and appropriate regulatory projects run smoothly, additional talent is being sought in REACH - Regulatory Affairs segment. For dossier preparations ...
Job Description Job description The Regulatory Manager will play a key role in delivering the regulatory strategy in the UK for the product portfolio. Reporting to the Head of Medical and Regulatory Affairs, you will be responsible for managing a team of Regulatory Advisors in order to maintain the existing product portfolio and get new products to market. You will provide Regulatory input to the busi...
6-12 Months- REACH Registration Specialist- Chemicals- IUCLID, SIEFs + Product Stewardship. Based in the West Midlands our client is a renowned chemical solutions business seeing a surge in the demand and growth simultaneously. To ensure that REACH Registration projects of customers and appropriate regulatory projects run smoothly, additional talent is being sought in REACH - Regulatory Affairs segment. For dossier preparations ...
Our client a Global leader in the development of revolutionary veterinary and animal health medicines is currently seeking a passionate Licensing Manager to deliver the regulatory and safety strategy for all products across Global markets and to ensure ongoing compliance. The role will require the successful candidate to deliver assigned brands to new markets with maximum competitive advantage focusing on the use of regulatory knowledge to ...
An opportunity has arisen for a Materials Officer to focus on monitoring voluntary and regulatory actions relating to these sustainability issues which impact the tin market in a positive or negative way. This work will also entail assisting in providing an appropriate response to regulators, industry or other stakeholders in order to obtain the optimal outcome for the tin industry as a whole. The successful candidate will also be...
Experienced Regulatory Affairs Assistant required for our client, a professional and leading company within its field. This is a long term temporary assignment paying around £13 per hour. You will be providing comprehensive secretarial and administrative support to a large regulatory affairs team, ensuring the department runs smoothly and efficiently during this busy time. Your main focus will be to offer the following; <b...
Organisation Description Reed Scientific are currently recruiting a Regulatory Specialist, to support validation activities associated with the delivery of product transfer project work. The roles will be part of a team supporting site transfer projects from one facility to another and are intended to be for a fixed 2 year period with flexibility to extend the contract. Job Description <br /...
6-12 Months- REACH Registration Specialist- Chemicals- IUCLID, SIEFs + Product Stewardship. Based in the West Midlands our client is a renowned chemical solutions business seeing a surge in the demand and growth simultaneously. To ensure that REACH Registration projects of customers and appropriate regulatory projects run smoothly, additional talent is being sought in REACH - Regulatory Affairs segment. For dossier preparations ...
Regulatory Affairs Specialist - REACH - Toxicology - Eco toxicology - Pharmacology - Cosmetics / Personal Care - London - Permanent - £30-35K + Benefits An international leader in the Cosmetics and Personal Care market is currently seeking to appoint a Regulatory Affairs Specialist to work as part of the groups Compliance Division, Product Safety and Regulatory Affairs Dept. based in West London. You will need to...
The Company: A global biopharmaceutical company involved in the discovery, development & commercialisation of treatments for severe conditions. They currently have hundreds of clinical trials active globally focusing on mostly incurable conditions. They employ thousands of people world wide and has grown to this size from relatively humble beginnings over 30 years ago. The Role This is a new role that wi...
Job Description Our client – a risk management services company based in Buckinghamshire, are currently seeking part-time, home based workers to write COSHH risk assessments for them. The computer programme you will be using will be web-based, so all you need is a PC and internet access to complete the work. A minimum weekly number of assessments you need to complete will be set, though it is thought that ...
CMC Regulatory Consultant - part time; Home Based, Negotiable Rate A rare opportunity for a CMC Regulatory Affairs professional who would like completely flexible, part-time hours. The role is with a small but successful and expanding consultancy providing regulatory services to the pharma and consumer health industries. The role can be home based and has totally flexible hours, subject to project deadlines. The work wi...
CMC Regulatory Consultant - part time; Home Based, Negotiable Rate A rare opportunity for a CMC Regulatory Affairs professional who would like completely flexible, part-time hours. The role is with a small but successful and expanding consultancy providing regulatory services to the pharma and consumer health industries. The role can be home based and has totally flexible hours, subject to project deadlines. The work wi...
CMC Regulatory Consultant - part time; Home Based, Negotiable Rate A rare opportunity for a CMC Regulatory Affairs professional who would like completely flexible, part-time hours. The role is with a small but successful and expanding consultancy providing regulatory services to the pharma and consumer health industries. The role can be home based and has totally flexible hours, subject to project deadlines. The work wi...
CMC Regulatory Consultant - part time; Home Based, Negotiable Rate A rare opportunity for a CMC Regulatory Affairs professional who would like completely flexible, part-time hours. The role is with a small but successful and expanding consultancy providing regulatory services to the pharma and consumer health industries. The role can be home based and has totally flexible hours, subject to project deadlines. The work wi...
CMC Regulatory Consultant - part time; Home Based, Negotiable Rate A rare opportunity for a CMC Regulatory Affairs professional who would like completely flexible, part-time hours. The role is with a small but successful and expanding consultancy providing regulatory services to the pharma and consumer health industries. The role can be home based and has totally flexible hours, subject to project deadlines. The work wi...
CMC Regulatory Consultant - part time; Home Based, Negotiable Rate A rare opportunity for a CMC Regulatory Affairs professional who would like completely flexible, part-time hours. The role is with a small but successful and expanding consultancy providing regulatory services to the pharma and consumer health industries. The role can be home based and has totally flexible hours, subject to project deadlines. The work wi...
Job Description My client is looking for a Regulatory Affairs Assistant to assist the Regulatory Affairs Manager in providing regulatory support for domestic and international registrations of their manufactured product. Key duties include: - Liaising with the International Commercial team to organise, prepare and assist with submitting documentation to support international product ...
Outcomes Research Manager - initial 6 months contract Office based near Tadworth, Surrey Major international pharmaceutical organisation Plan, design and conduct multi-national OR studies Ongoing contract position with competitive hourly rate Summary A "top three" global pharmaceutical company is seeking an experience...
Regulatory Affairs -Medical devices This permanent position and great opportunity at a global business, you will principally be responsible for providing input and support to RA of medical device, IVD and Class I to III, including: Advising on appropriate regulatory pathways Risk management throughout the product lifecycle Review and approval of design inputs and requirements Design va...
Due to expansion there is now a vacancy for a Regulatory Affairs Officer to join a global pharmaceutical company at their site in Slough, Berkshire. Regulatory Affairs Officer will be offered a salary of c£35,000 + pension + healthcare + life assurance. Role reports to the Regulatory Affairs Manager. MAIN PURPOSE: To provide regulatory advice and support to the UK affili...
Due to expansion there is now a vacancy for a Regulatory Affairs Officer to join a global pharmaceutical company at their site in Southampton, Hampshire. Regulatory Affairs Officer will be offered a salary of c£35,000 + pension + healthcare + life assurance. Role reports to the Regulatory Affairs Manager. MAIN PURPOSE: To provide regulatory advice and support to the UK ...
Our established Pharmaceutical client based in Walton Oaks, Surrey is looking for an Artwork Change Specialist to join their team on a 1 year long contract. Job purpose: · This is a pure Artwork role. · Working on current Product portfolios. · P...
Job Description Our client, a leading CRO based in Berkshire, urgently requires an Ecotoxicology Section Manager to join its technical function. You will be familiar with working within a GLP environment to OECD/US EPA OPPTS/JMAFF guidelines, and have knowledge of terrestrial and aquatic ecotoxicology. The ideal candidate will have knowledge and/or experience of the Home-office licencing system, preferably ...
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Date: 17 May
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Norwich, Norfolk
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£40,000 per annum, negotiable, pro-rata, inc benefits
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0 applications
Regulatory Affairs Manager - PHARMA - Norfolk - Circa 40k Position: Regulatory Affairs Manager OR Senior Regulatory Officer Type:  ...
