Assistant Regulatory Manager

JR United Kingdom; Wolverhampton; On-site; GBP 35,000 - 50,000; Full time

Job summary

A global leader in Footcare seeks an Assistant Regulatory Manager in Wolverhampton. This role involves supporting regulatory compliance, optimizing processes for product registration, and providing training within the Global Regulatory Footcare team. Suitable candidates will have a scientific background and at least 2 years of regulatory experience, ensuring effective market entry for innovative products.

Qualifications

• At least 2 years of relevant regulatory experience.
• Experience with dossier creation and global registration.
• Knowledge of regulatory classifications.

Responsibilities

• Support registration and regulatory requirements across multiple markets.
• Prepare and review regulatory documents for product registration.
• Maintain regulatory databases with accurate records.

Skills

Regulatory Compliance

Documentation Preparation

Quality Management Systems

Product Development Regulations

Relationship Building

Ability to Work Under Pressure

Education

Honours degree in a scientific field

Tools

ISO 13485

Job description

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Assistant Regulatory Manager, Wolverhampton

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Job Category: Other

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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 in Footcare, with a portfolio that includes 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, facilitate the rollout of existing products, and ensure regulatory compliance. They will work to support regulatory planning across innovation and provide SME knowledge on core dossier requirements.

The role involves ensuring regulatory activities are completed efficiently and consistently across projects.

The Role

• Support registration and regulatory requirements across multiple markets to enable global pipeline delivery.
• Define processes and procedures within the Global Regulatory Footcare team to optimize speed to market.
• Prepare and review regulatory documents for product registration.
• Keep up-to-date with regional and national regulations and guidelines.
• Participate in product development and marketing projects for local and international launches.
• Maintain regulatory databases with accurate records.
• Provide regulatory training and support to teams.
• Develop regulatory strategies for successful product registration and variations.
• Build knowledge and intelligence within the Regulatory Function for a 'right first time' approach.
• Collaborate with partner functions to meet market-specific data requirements.
• Develop relationships with local regulatory contacts to facilitate efficient market entry.

The Requirements

• Honours degree in a scientific field or equivalent experience.
• At least 2 years of relevant regulatory experience, including dossier creation and global registration.
• Experience with quality management systems like ISO 13485.
• Knowledge of regulatory classifications such as Medical Devices, Cosmetics, REACH, or Biocides.
• Understanding of regional and global regulatory environments.
• Experience in preparing dossiers, variations, renewals, and updates.
• Knowledge of global product development regulations and guidelines.
• Ability to deliver high-quality work under pressure.