Are you a business? Hire regulatory affairs candidates in United Kingdom
Review, approve and/or issue technical Regulatory documentation to support EU/UK launches to ensure complete and accurate of Cosmetic Product Information Files (PIFs), CPNP/SCPN notifications, registration dossiers, claims substantiation and the management of Cosmetic Product Safety Reports (CPSRs). Act as the expert on PIF requirements, train and guide other team members as applicable. Carry out maintenance and product lifecycle related activities Provide UK-specific support, including UK REACH related activities Follow-up with other internal functions (Product Development, Artwork planners, Initiative leaders, packaging, MD…) as to resolve questions related to the documentation. Commission and oversee third party partners to ensure that all products have been assessed for consumer safety and regulatory compliance and take accountability for the quality of the output. Design, maintain and update internal guidelines and processes. Ensure all Farla & customer requirements are met. This includes the requirements of; The Vegan Society, Cruelty Free International (CFI) and Round Table for Sustainable Palm Oil (RSPO) etc. Managing an effective global regulatory horizon scanning process to ensure our regulatory processes remain future-fit. Competencies An experienced regulatory professional with a minimum of 2-3 years in a Cosmetic industry with detailed knowledge and understanding of the UK/EU Cosmetic regulations, US FDA (MoCRA) and other global regulations. Master the European cosmetic regulation and requirements for product registration in various countries, including China. Are fluent in English Self-starter, you like to learn about new area and develop your expertise. proficiency with MS-Office and high command of IT in general. Quick learner of new software and systems and good ability to present and train others.
The Manager, Global Aggregate Reports Quality and Compliance is an integral member of the Global Aggregate Report office and PV Writing Organization. The position holder responsibility includes the entire CSL product portfolio and development pipeline. Responsibilities include: - Acts as a Regu...
Location: Addlestone, Surrey KT15 3LS \n\nSalary: £35,857 - £38,551 per annum + 25 days Annual leave + Pension Scheme \n\nContract type: Permanent \n\nWorking pattern: Flexible working, Full-time, Job share, Part-time \n\nThe Veterinary Medicines Directorate (VMD) is an Executive Agency of the De...
Regulatory Affairs Advisor) reporting into the Technical Manager. Based at our Gravesend site.Joining us on a full time, permanent basis (Monday to Friday, 8.30-5.30, 40hours), you will receive a competitive salary. Moove is a leading provider of automotive lubricants, oils, and chemicals throug...
CK Group are recruiting for a Regulatory Consultant to join a company in the Pharmaceutical industry at their site based in High Wycombe on a contract basis for 6 months. Salary: Up to £64.00 per hour PAYE or £86.00 per hour UMB Regulatory Consultant Role: Regulatory review and appro...
Planet Pharma are currently partnered with a global pharmaceutical manufacturing company who are actively seeking a Automation Project Manager for a permanent position in their UK team. The ideal candidate : experience working within manufacturing and packaging. knowledge of the automation projec...
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Cobalt Housing is a registered housing association based in North Liverpool. Cobalt was formed in February 2003 following the transfer of our homes from Liverpool City Council. The organisation manages and maintains around 6000 affordable homes in the Fazakerley & Sparrow Hall, Croxteth and Norri...
Reporting to the Senior Regulatory Affairs Officer, this role supports the Regulatory team with post-approval activities for the product portfolio. Able to demonstrate a genuine interest and knowledge of the regulatory environment and a desire to succeed in a regulatory affairs role in the pharma...
Role: Labelling Manager Duration: 6 Months Location: 2 days on site at High Wycombe Responsibilities and Deliverables: • Regulatory review and approval of product labelling for Cosmetics and other non-OTC classes per the company portfolio in mainly UK & Ireland • Regulatory review and approval an...
Acting as the mentor for less experienced staff, the Regulatory Affairs Manager will be leading the communication and negotiation with other regulatory bodies. An exciting opportunity for an experienced Regulatory Affairs Manager to join a leading manufacturer of high quality biocide products. As...
Regulatory Affairs Specialist .Month Contract – Outside IR35.Buckinghamshire, UK – 2 days on-site per week.Per Hour via Limited or Umbrella.An opportunity to join a global leading consumer health business and be responsible for supporting UK and Ireland Cosmetic and non-OTC submissions.The role w...
Life Sciences degree or equivalent. ...
Regulatory Affairs Advisor (French Speaking).At Campden BRI, we have a dedicated Regulatory Affairs Team who offer a valuable and expert advisory service, as we're the leading authority, helping our clients stay compliant with food regulations in more than 80 countries! We are widely recognised f...
The Manager, Regulatory Affairs International supports our ambitious geographical expansion plans. Develop International regulatory strategies and filing plans, in partnership with the Global Regulatory Lead, and country leads, for assigned products in development. Develop regulatory strategies i...
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. Ensure the submission str...
Regulatory Affairs Advisor (Arabic Speaking). At Campden BRI, we have a dedicated Regulatory Affairs Team who offer a valuable and expert advisory service, as we're the leading authority, helping our clients stay compliant with food regulations in more than 80 countries! We are widely recognised ...
The Director, Strategy, Regulatory Sciences will be responsible for formulation and implementation of regulatory strategies and recommendations for the resolution of complex issues for clients and will lead the process in the development of regulatory submissions, including but not limited to sci...
Conducts regulatory impact assessment and provide appropriate regulatory strategy for these changes that requires regulatory actions. Working with internal concerned departments, prepares appendices attached to regulatory CMC documents to be submitted to regulatory authority and submits them. CMC...
They are recruiting for a Regulatory Affairs Officer to join their Regulatory Affairs & Quality team; the role is a full permanent position working flexible working hours and with hybrid working. You will be responsible for building regulatory strategy, applicable regulatory requirements, solutio...
Lead Design Engineers and Graduate Engineers within the technical team and be accountable for scheme design, consultancy / feasibility studies, technical standards, regulatory affairs and associated legal processes. The Senior Designer Engineers will have overall responsibility for creating desig...
The business is currently looking for a Regulatory Affairs Manager to join the business and take the lead on all Regulatory Affairs activities. Regulatory Affairs Manager (Food & Beverages). The role will support a number of UK, European, and global projects supporting end-to-end regulatory proce...
... Advisor (Fluent in german) to join our client's team to check and approve specifications and ... You will be accountable for quality, accurate and timely risk-based advice, which enables our ...
Senior Director or Director of Regulatory Affairs Strategy Location: Harwell, UK Hybrid Working ... Experience in the regulation of biologics, including immunomodulating therapies and vaccines, is ...