Senior Regulatory Affairs Specialist

Hologic; Cambridge; Presencial; GBP 40 000 - 50 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Pension

Insurances

Resumo da oferta

Hologic is seeking a Senior Regulatory Affairs Specialist in Cambridge to lead regulatory submissions, manage technical files, and support global regulatory activities for medical devices.

You will work with R&D, Quality, Clinical, and Marketing to ensure compliance across US, EU, and Canada, contributing to product lifecycle management and inspection readiness.

Qualificações

• Experience in the regulated medical device industry and product lifecycle.
• Hands-on regulatory submissions, technical files, audits, inspections, and investigations.
• Knowledge of US FDA, EU, Canadian regulations and ISO 13485/9001.

Responsabilidades

• Prepare and compile document packages for regulatory submissions, audits, and license renewals.
• Support regulatory activities for new and mature medical device products.
• Review labeling, manuals, and marketing content for regulatory compliance.
• Monitor regulations and translate changes into practical guidance.
• Participate in internal and external audits and inspections.
• Provide regulatory input on design reviews and manufacturing changes.

Conhecimentos

Regulatory submissions

Regulatory strategy

Technical writing

Cross-functional collaboration

Audit/inspection support

Regulatory databases

Formação académica

Bachelor’s degree or technical degree (scientific/engineering)

Descrição da oferta de emprego

Senior Regulatory Affairs Specialist - Cambridge

At Hologic, we are committed to enabling healthier lives everywhere, every day. To deliver on that purpose, we need strong regulatory expertise that helps bring new products to market, keeps mature products compliant, and ensures our submissions, labeling, technical files, and product documentation meet global regulatory expectations.

We are looking for a Senior Regulatory Affairs Specialist to support regulatory submissions, audits, inspections, technical documentation, and product lifecycle activities for medical devices. This role is ideal for a regulatory professional with strong knowledge of US, EU, and Canadian requirements who enjoys working cross-functionally with Regulatory Affairs, R&D, Clinical, Quality, Marketing, and international regulatory teams.

What to expect:

• Prepare, coordinate, and compile document packages for regulatory submissions, audits, inspections, license renewals, and annual registrations.
• Support regulatory activities for new and mature medical device products, including product changes and ongoing compliance.
• Manage and maintain regulatory databases, technical files, and supporting documentation.
• Review technical data, reports, labeling, marketing materials, user manuals, and other product content for regulatory compliance.
• Support compliance with US, EU, Canadian, and international regulatory requirements.
• Manage labeling and unique device identification requirements.
• Provide regulatory input on design reviews, manufacturing changes, clinical protocols, and product approval strategies.
• Document regulatory decisions and ensure documentation remains current, accurate, and inspection-ready.
• Participate in internal and external audits, inspections, and investigations.
• Monitor evolving regulations, standards, and procedures, and translate changes into practical business guidance.
• Contribute to process, procedure, standard, and tracking/control system improvements.Partner with cross-functional teams to resolve regulatory issues and support timely product approvals.

What we expect:

• Experience in the regulated medical device industry, ideally supporting product lifecycle and regulatory compliance activities.
• Hands-on experience with regulatory submissions, technical files, product documentation, audits, inspections, and investigations.
• Strong understanding of US FDA, EU, Canadian, ISO 13485, ISO 9001, and other applicable international regulatory requirements.
• Ability to review labeling, marketing materials, user manuals, technical documentation, and supporting data from a regulatory perspective.
• Strong technical writing, communication, interpersonal, and presentation skills.
• Good data and statistical analysis skills, with the ability to make informed recommendations.
• High attention to detail and strong judgment when evaluating regulatory issues and solutions.
• Confidence working cross-functionally with Regulatory Affairs, R&D, Clinical, Quality, Marketing, and global partners.
• Proficiency with Microsoft Office and confidence working with regulatory databases or tracking systems.
• A college degree or technical bachelor’s degree, preferably in a scientific, engineering, or related discipline.
• Regulatory Affairs Certification — RAC — or project management experience would be beneficial.

Why join Hologic?

At Hologic, your work has purpose. You will be part of a company focused on improving health through innovation, quality, and regulatory excellence.

We are committed to making Hologic a destination for top talent. From the moment you join, we provide comprehensive training, ongoing development, and the tools and knowledge you need to succeed and grow your career.

Salary: £40,000 – £50,000 gross per year

The final offer will depend on experience, skills, and alignment with internal pay structures. In addition, we offer a comprehensive benefits package including pension and insurances.