Are you a business? Hire regulatory affairs manager 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...
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...
Alliance Healthcare is a leading international provider of pharmaceutical wholesaling, logistics, support with clinical trials, and other innovative healthcare services and solutions to independent pharmacists and pharmaceutical manufacturers across Europe and beyond. It is an exciting time for A...
Employers want to know
Do you have work experience?
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. ...
Life Sciences degree or equivalent. ...
Senior Manager, Regulatory Affairs. ...
Are you familiar with UK and EU REACH regulations? Looking for a role that provides a work life balance but also a fulfilling career?.An exciting opportunity for an experienced Regulatory Affairs Manager to join a leading manufacturer of high quality biocide products.As a Regulatory Affairs Manag...
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...
Our client, an independent pharmaceutical company who manufacture and specialising in generics, have an opportunity for an experienced EU/ UK Regulatory team leader to join their team in Hampshire.As Regulatory Affairs manager, you will:.Leading a small team, handling the regulatory activity acro...
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...
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...
Reporting to the Regulatory Affairs Manager, you will play a crucial role in ensuring regulatory compliance and supporting the successful submission of our products to global regulatory agencies. As ...
We are looking for a Microbiology Laboratory and Quality Assistant, on a full time basis, to work closely with the Quality Assurance & Regulatory Affairs Manager, to progress ongoing and one-off ...
Top 3 skills needed for this role: * Stakeholder management * Organisation/prioritisation ... About The CompanyVitality is a multi-award-winning UK insurance brand, here to make the world a ...
Reporting to the Regulatory Affairs Manager, you'll take on the crucial responsibility of coordinating all required post-market activities, ensuring compliance with regulatory reporting timelines ...
Interested in joining our team at TCS Biosciences Ltd? We are looking for a Quality Assurance & Regulatory Affairs Manager to join our team on a full time basis. Quality Assurance & Regulatory ...
... products. * Proven experience in creating RA strategies for new MAAs and VA submissions. * Has direct line management experience (3-5 people). * Good communication skills. Regulatory Affairs | RA ...
... Executive (HSE). Customs and Excise regulations and controls apply from the moment cereals are ... We provide a cycle to work scheme, BUPA healthcare, life assurance and group income protection ...
Excellent communication skills both oral and written If you are a highly motivated individual with ... Hybrid working with 2 days in the office and 3 days from home.
... policy into company processes with alignment to regional regulatory strategy. For example key ... Maintenance of existing products in light of growing Safety, Regulatory & Environmental issues and ...
Topics include the holding and movement of excise goods, customs controls and processes, verification and alcohol fraud. The role will provide the opportunity to lead on these two important topics ...
Preparing and delivering reports and summaries of regulatory publications and assisting in preparing responses to regulatory consultations and other such papers * Executing key regulatory processes ...