Average Regulatory Specialist salary in the UK

My client, a forward-thinking medical device company at the forefront of bioelectronic medicine. Their mission is simple, they're set to revolutionise healthcare by developing cutting-edge therapies for individuals battling chronic diseases. With their breakthrough, they have been granted the Breakthrough Device Designation by the United States FDA, enabling accelerated market access for devices addressing life-threatening or irreversibly debilitating conditions. Senior Regulatory Affairs Specialist As the Senior Regulatory Affairs Specialist, you will serve as the regulatory expert responsible for guiding the development and launch of an innovative medical device system. Your role involves collaborating with international regulatory consultants to enhance the organisations global regulatory strategy. You will closely coordinate with R&D, clinical, market access, and quality teams to ensure adherence to regulatory and legal requirements for successful market authorisation across the EU, USA, and other regions. As the primary point of contact with competent authorities, notified body, EU expert panel, and FDA, you will oversee the preparation and follow-up of FDA pre submissions, CE-mark dossiers, and other regulatory submissions, taking ownership of these critical processes. Senior Regulatory Affairs Specialist Responsibilities: Spearhead the development and execution of the regulatory strategy to secure approvals from regulatory agencies such as the FDA and CE-marking, ensuring continuous compliance across the product lifecycleAct as the primary point of contact for regulatory submissions, reporting, and follow-ups with Competent Authorities, FDA, Notified Body, and other regulatory entitiesLead the coordination, preparation, and submission of regulatory documents, ensuring accuracy and completenessOffer regulatory guidance and assistance for post-market surveillance activities, including the management of adverse event reporting and product complaintsStay updated on regulatory changes and evolving standards that may impact the product portfolio, proactively integrating necessary adjustments and ensuring compliance Senior Regulatory Affairs Specialist Responsibilities: Possess an academic background in a relevant discipline, such as science, medicine, or pharmacy, coupled with a keen interest in (medical) technologyDemonstrate a minimum of 5 years of recent and proven experience in regulatory affairs within the medical device industryShowcase firsthand experience in securing regulatory approvals for medium-risk or high-risk medical devices in both the EU and/or USA marketsExhibit an analytical mindset and exceptional writing skills, coupled with the ability to structure tasks effectively and independently initiate projects As the Regulatory Affairs Specialist, you'll pioneer transformative therapies for chronic diseases like. You'll navigate complex regulatory landscapes, ensuring devices reach those in need swiftly. This role offers a chance to make a tangible difference worldwide, contributing to a transformative vision in healthcare. If this opportunity is of interest, please apply with an up to date CV right away.

SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote. The Role: The Regulatory Associate is responsible for providing global regulatory expertise for Clinical Trials. They are the primary interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes. Key Responsibilities: § Manage a portfolio of CTAs including preparation and distribution of documentation associated with new initial CTAs and all CTA maintenance activities such as substantial amendments, end of trial notifications etc. § Provide advice on submission strategy, country requirements, etc. as well as operational support for Regulatory submission preparation and processing of amendments. § Review of and input on documents related to clinical trial submissions managed by other stakeholders. § Ensure approved company CTA processes are followed within agreed timelines. § Review and maintain awareness of regulatory intelligence relating to clinical trials and advise stakeholders accordingly. § Ensure all relevant databases and activity trackers are populated within agreed timelines. § Provide technical support on document preparation. § Undertake all necessary training in order to achieve compliance with internal/external processes. § Provide operational support for the Clinical Trial Strategy & Submissions Team as required. § Comply with the company's policies and procedures. Skills/Experience Require Education Required: Bachelor's degree in medicine, pharmacy, biology, chemistry, pharmacology, or related life sciences subject is required. Preferred: Relevant advanced degree in life sciences is preferred § At least 2-years CTA experience in global clinical trial submissions to regulatory agencies. § Experience working effectively across cultures and in a complex matrix environment. § Good Information Technology skills, proven ability to utilise a variety of computer application packages. § Proactive verbal and written communication style at all levels. § Has excellent communication/presentation skills, written and verbal; fluency in English. § Strong proven personal development and motivational skills. § Strong interpersonal, organisational and team working skills. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

We are currently recruiting for two Regulatory Specialists to join a Milton Keynes based company, in a 1-year fixed term contract. Overview: The successful candidate will support internal customers including: Customer Service team, Sales reps, Research & Development team, and Quality Assurance team by serving as an expert in assigned areas. You will need to: Interpret regulations, by providing information to address external customer needs.Provide guidance in the development of products to internal customers by accurately maintaining product information databases.You will also support external customers by providing routine or standard technical information in areas of subject matter expertise / core technology. Duties: Maintain up-to-date awareness and knowledge of the principles set forth in the food regulations for assigned core technologies, ingredient categories and associated regulatory agencies.Actively cross-train with others to relieve high volume issues and maintain a balance of workload within the department.Communicate information to appropriate personnel. Actively listen and share information and knowledge with others in an effective and a timely manner whilst ensuring that appropriate information is communicated, received and understood.Demonstrate the technical/functional skills required to fulfil the needs of the role and continually develop expertise. You will actively and continuously engage in personal development aimed at improving your current skills and developing additional skills in order to effectively apply expertise internally and externally.Travel on a non-routine basis. Skills Required: Bachelor of Science degree in food science, chemistry or related field or equivalent qualification.2-3 years’ experience in regulatory affairs within the food industry.Strong communication skills in English and one other Western-European language, to be able to actively listen and share information and knowledge with others in an effective and a timely manner. Benefits: Opportunity to collaborate with your colleagues, onsite 5 days per week.An excellent salary, benefit offering and development opportunities.A thorough and effective training experience during onboarding and beyond.Opportunity to develop a strong and fulfilling career.