Senior Regulatory Affairs Specialist

Hologic; St. Ives; Sur place; GBP 40 000 - 50 000; Plein temps

Avantages offerts par ce poste

Pension

Insurances

Résumé du poste

Hologic is seeking a regulatory affairs professional to prepare and coordinate regulatory submissions, maintain technical files, and ensure compliance across US, EU, Canada and international markets. You will review labeling, marketing materials, user manuals, and product content for regulatory adherence, and support audits, inspections, and ongoing lifecycle activities.

The role requires collaboration with R&D, Quality, Marketing, and global partners, proficiency with regulatory databases, and

Qualifications

• Experience in regulated medical device industry and lifecycle support.
• Strong technical writing and ability to review labeling, data and docs.
• Familiarity with US FDA, EU, ISO 13485, ISO 9001 and international regs.

Responsabilités

• Prepare, coordinate, and compile regulatory submissions and documents.
• Review labeling, manuals, and marketing content for compliance.
• Support audits, inspections, and lifecycle regulatory activities.
• Maintain regulatory databases and technical files with accuracy.

Connaissances

Regulatory affairs

Technical writing

Cross-functional collaboration

Data analysis

Attention to detail

Formation

Bachelor's degree in Science/Engineering

Outils

Regulatory databases

MS Office

Documentation tools

Description du poste

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.

• 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.

• 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.

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.

If you are a regulatory affairs professional who enjoys technical documentation, submissions, cross-functional partnership, and supporting products throughout their lifecycle, we would welcome your application.

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.