0 Financial Regulations jobs in the United Kingdom

What does 'family business' mean to you?

For some, it's code for small, for others it is a collaborative and friendly space.

The truth - it's usually both.

Family, small to midsized pharmaceutical companies look after their staff. You become part of their community, their culture, and the way they do things.

In our experience, staff at family run SMEs experience longer levels of employment than at large global corporations, and are often compensated well over time for their rewards.

Which is why, I am delighted to be representing a leading (family run) pharmaceutical manufacturing organisation based near Watford in the UK.

This amazing company are going through a great transformation that should ensure the company's future for generations to come, and as part of that they are looking for reliable, professional and hard working Regulatory Affairs professionals.

As part of this expansion, our client is looking for someone with 5+ years experience in Pharmaceutical Regulatory Affairs (ideally in a similar style of company, but they are open to people from all different pharmaceutical organisations).

You need to have a hard working attitude, good attention to detail, and you need to be able to work well with your team. Your experience in eCTD manager and document management tools will be valued, and you will need knowledge of global Regulatory requirements and guidelines (MHRA, EMA and ICH).

This is a site based role near Watford (5 days per week) and would suit someone looking for a company they can grow with, and build with, and that will give them huge career tragectory in a culture that is supportive and dynamic.

Interested? Apply Now!

What does 'family business' mean to you?

For some, it's code for small, for others it is a collaborative and friendly space.

The truth - it's usually both.

Family, small to midsized pharmaceutical companies look after their staff. You become part of their community, their culture, and the way they do things.

In our experience, staff at family run SMEs experience longer levels of employment than at large global corporations, and are often compensated well over time for their rewards.

Which is why, I am delighted to be representing a leading (family run) pharmaceutical manufacturing organisation based near Watford in the UK.

This amazing company are going through a great transformation that should ensure the company's future for generations to come, and as part of that they are looking for reliable, professional and hard working Regulatory Affairs professionals.

As part of this expansion, our client is looking for someone with 5+ years experience in Pharmaceutical Regulatory Affairs (ideally in a similar style of company, but they are open to people from all different pharmaceutical organisations).

You need to have a hard working attitude, good attention to detail, and you need to be able to work well with your team. Your experience in eCTD manager and document management tools will be valued, and you will need knowledge of global Regulatory requirements and guidelines (MHRA, EMA and ICH).

This is a site based role near Watford (5 days per week) and would suit someone looking for a company they can grow with, and build with, and that will give them huge career tragectory in a culture that is supportive and dynamic.

Interested? Apply Now!

• The Regulatory Affairs Consultant EMEA (Self Care) is responsible for the development of regulatory strategies across the EMEA region, and globally as relevant, providing regulatory input and technical guidance on regulatory requirements to product development teams within the Self Care franchise.
• Evaluates and coordinates the regulatory deliverables for medicines and food supplements, within their geographical and/or brand area of responsibility.
• Prepares and submits regulatory submissions according to applicable regulatory requirements and guidelines.
• Tracks the status of applications under regulatory review and provides updates to the regulatory team.
• Works with local and regional regulatory colleagues to develop global and/or regional regulatory strategies, coordinating regulatory actions and results and develops global/regional dossiers to support local review processes

• Relevant Bachelor's Degree or higher in Life Sciences, Chemistry, Pharmacy
• Expertise across a broad spectrum of Regulatory classifications in particular medicine and food supplements in EMEA region
• Strong knowledge of regulatory frameworks and external environments, and the ability to apply these to regulatory solutions throughout the product lifecycle.
• Solid understanding of regulatory/medical/safety/quality requirements in the markets of relevance.
• In-depth knowledge of the business, organizational goals, Regulatory Affairs function, and cross functional business partners to make informed business decisions and create and execute business strategies. Ability to represent RA function on cross-functional teams and governance forums.

Regulatory Affairs Lead - MedTech

A growing MedTech company is seeking an experienced Regulatory Affairs Leader . The ideal candidate will act as the key liaison between the business, its products, and regulatory bodies, with responsibility across pre- and post-market regulatory activities.

We’re looking for someone with strong experience in Medical Devices/Technology regulatory frameworks (including FDA submissions and international standards) who can guide products from development through to market launch and beyond.

This individual will act as the expert in taking Class IIa products through the regulators and act as a standlone Subject Matter Expert in FDA510(k) and wider areas.

Key responsibilities:

• Provide regulatory guidance to internal teams and senior management, supporting the preparation and submission of regulatory documentation.
• Maintain and update regulatory files and tracking systems to ensure timely access to approval and renewal information.
• Ensure products comply with regional and international regulations and standards.
• Keep abreast of evolving legislation, guidelines and industry practices.
• Analyse and present scientific data to support new product approvals and renewals.
• Manage submission timelines for licence variations and renewals, ensuring deadlines are met.
• Prepare and review product labels, patient information leaflets and related documentation.
• Advise on product testing requirements and interpret clinical and technical data.
• Offer strategic regulatory input during product development and updates.
• Lead or coordinate regulatory inspections and audits.
• Liaise and negotiate with regulatory authorities to secure product authorisations.
• Support process improvements and provide compliance training and advice to teams.

About You:

• Strong industry experience operating in a Lead level role within Regulatory Affairs (E)
• Experience working with Medical Devices/Technology in a regulated environment; Class IIa devices and above (E)
• Candidates must have experience working with electronics based devices (E)
• Strong experience in leading FDA 510(k) submissions (E)
• Wider experience in 60601-1 and SaMD would be beneficial (D)
• Proven ability to manage regulatory processes, leading Class IIa device accreditation with regulators (E)
• Collaborative, organised and able to manage multiple projects and deadlines (E)

Candidates must have experience as a Lead within FDA510(k) and be at a level to work as a sole expert, and be able to visit the company office once a week.

Join a Science-Led Consumer Healthcare Pioneer on an Exciting Growth Journey

Are you ready to be part of something extraordinary? At Alliance, we're a dynamic, science-led consumer healthcare organisation specialising in advanced skincare solutions and vitamins, minerals & supplements (VMS). Backed by innovation and driven by purpose, we're on an exciting journey of transformation and growth — expanding our reach, enhancing our brands, and bringing cutting-edge products to more consumers across the globe.

As we continue to evolve, we’re looking for passionate, curious, and driven individuals to join us. If you’re excited by the opportunity to shape the future of health and wellness in a fast-paced, entrepreneurial environment — this is your moment.

Are you passionate about regulatory affairs in the food supplement or cosmetics sector and excited to shape the future of global innovation? Join our Global Regulatory team at Alliance, where you’ll play a vital role in ensuring compliance while enabling the successful launch of innovative products across international markets.

As a Regulatory Affairs Associate (known as a Regulatory Scientist internally) you’ll act as a subject matter expert in food supplement or cosmetic regulations, providing expert advice and guidance to cross-functional teams. You’ll be central to driving compliance, supporting innovation, and influencing regulatory change in a fast-paced and collaborative environment.

What You’ll Be Doing

• Supporting the implementation of robust regulatory strategies to ensure compliance and commercial success.
• Providing regulatory expertise to innovation projects, enabling smooth and timely product launches.
• Creating, maintaining, and approving regulatory documentation, including submissions to databases.
• Maintaining the EMEA food supplement or cosmetics portfolio and supporting medical device compliance.
• Leading departmental Quality Management System (QMS) activities and supporting audits, SOPs, and CAPAs.
• Representing regulatory affairs in cross-functional meetings, offering clear advisory input.
• Contributing to industry consultations, forums, and discussions to influence regulatory best practices.
• Driving continuous professional development for yourself and supporting knowledge growth within the team.

What we’re looking for

We’re seeking someone who brings both technical expertise and a collaborative mindset. You’ll have:

• A degree (BSc/MSc) in Life Sciences, Nutrition, Food Science, Pharmacy, Chemistry or related discipline.
• Solid knowledge of UK/EU food supplement or cosmetic regulations (with global exposure desirable).
• Familiarity with medical device regulations (EU Cosmetics Regulation, MDR, ISO standards).
• Experience preparing, reviewing, and submitting regulatory dossiers, notifications, and documentation.
• Working knowledge of QMS processes (SOPs, audits, CAPAs).
• Strong ability to interpret regulations, advise teams, and support compliance strategies.
• Proven track record of supporting new product launches through effective regulatory input.
• Excellent regulatory writing, documentation management, and database submission skills.

What we offer

• Competitive salary with discretionary bonus
• 25 days holiday + 1 celebration day + 1 volunteering day + bank holidays, with the option to buy up to 10 extra days
• Generous pension scheme (up to 10% employer contribution)
• Life assurance (4x salary)
• Private medical cover and health cash plan (with options for family cover)
• Wellbeing support: eye care, flu vaccine, EAP & discounts via Perks at Work
• Salary sacrifices options with the Cycle scheme and electric vehicle schemes
• Flexible working and family-friendly policies
• Global recognition programme & £1,000 referral bonus

If you are looking to make a difference and be part of something exciting, we’d love to hear from you

Cure Talent are delighted to be partnered with a rapidly growing medical device company with a diverse portfolio spanning IV therapy, diabetes care, surgical, anaesthesia, sexual health and more. As the business continues to expand, we have an exciting opportunity for a Regulatory Affairs Specialist to join their dedicated Quality & Regulatory team.

This is a hybrid role with the expectation of being on site in Uxbridge once a week.

As the new Regulatory Affairs Specialist, you will play a vital role in supporting all Quality and Regulatory activities across the business. You will contribute to the development and maintenance of regulatory documentation, ensure compliance with global standards, and support smooth implementation of evolving regulations, while working closely with internal teams and external stakeholders.

Key Responsibilities

• Support and maintain the company’s Quality Management System (QMS).
• Write, review, and maintain technical files and other regulatory documentation (MDD, MDR, IVDR, UKCA, FDA, Procedure Packs).
• Ensure compliance with UKCA, EU MDR, FDA and relevant ISO standards.
• Manage document control, updating procedures and product fact sheets.
• Support product development and UDI processes.
• Coordinate and support internal and external audits.
• Monitor regulatory and standards updates, ensuring timely implementation.

Experience and Skills Required

• Proven Regulatory Affairs experience within the medical device industry, across a range of device classes.
• Strong knowledge of ISO 13485.
• Science-based degree or equivalent.
• Logical, proactive problem-solving skills with strong attention to detail.
• Excellent report writing, organisational and time management skills.
• Strong interpersonal skills with the ability to work cross-functionally.
• Multi-language skills would be an advantage.

If you’re a Regulatory Affairs professional seeking an exciting opportunity to support a broad medical device portfolio and grow with a dynamic business, we’d love to hear from you.