Assistant Regulatory Manager

JR United Kingdom; Nottingham; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading global company in Footcare seeks an Assistant Regulatory Manager to enhance regulatory compliance and support product registration across markets. The role encompasses overseeing regulatory activities, developing strategies, and working with cross-functional teams to facilitate product innovation and compliance in the healthcare industry.

Qualifications

• At least 2 years of relevant regulatory experience.
• Experience with quality management systems.
• Knowledge of regulatory classifications.

Responsibilities

• Support registration and regulatory requirements across multiple markets.
• Prepare and review regulatory documents.
• Maintain regulatory databases.

Skills

Project Management

Regulatory Compliance

Communication

Analytical Skills

Problem Solving

Education

Honours degree in a scientific field

Tools

ISO 13485

Job description

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Assistant Regulatory Manager, Nottingham

Client:

Location: Nottingham, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views:

1

Posted:

04.06.2025

Expiry Date:

19.07.2025

Job Description:

Our client is a global leader within Footcare, with a portfolio across medical devices, cosmetics, orthotics, and personal care. They are looking to add an Assistant Regulatory Manager to their team.

The Assistant Manager will support the delivery of NPD/EPDs to global markets, oversee the rollout of existing products, and ensure regulatory compliance. You will support regulatory planning across innovation and provide SME knowledge on core dossier requirements relevant to the product portfolio.

You will ensure all regulatory activities are completed efficiently and consistently across projects.

The Role

• Support registration and regulatory requirements across multiple markets to deliver a global pipeline.
• Work with the Global Regulatory Footcare team to optimize processes and streamline efficiencies.
• Prepare and review regulatory documents for product registration.
• Keep up-to-date with regional and national regulations, guidelines, and advisory documents.
• Participate in product development and marketing projects for local and international launches.
• Maintain regulatory databases with accurate product records.
• Provide regulatory training and support to teams.
• Develop regulatory strategies for successful product registration and variations globally.
• Build knowledge within the Regulatory Function to ensure a 'right first time' approach.
• Collaborate with partner functions to meet market-specific data requirements and timelines.
• Establish relationships with local regulatory contacts to facilitate aligned plans and shared learnings.

The Requirements

• Honours degree in a scientific field or equivalent experience.
• At least 2 years of relevant regulatory experience in dossier/technical file creation and global registrations.
• Experience with quality management systems such as ISO 13485.
• Knowledge of regulatory classifications including Medical Devices, Cosmetics, General Products, REACH, or Biocides.
• Understanding of regional and global regulatory environments.
• Experience in preparing dossiers, variations, renewals, and technical updates.
• Knowledge of global product development practices, rules, and guidelines.
• Awareness of factors influencing the regulatory environment, including emerging guidelines.
• Ability to deliver high-quality work independently under pressure.