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Regulatory Operations Specialist - Medical Devices

Job in Hull, East Riding of Yorkshire, HU2, England, UK
Listing for: Reckitt Benckiser
Full Time position
Listed on 2026-08-17
Job specializations:
  • Healthcare
    Healthcare Compliance, Healthcare Management
Job Description & How to Apply Below
We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose.
Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege.​Research & Development​In Research and Development, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance.
We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.
The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.

About the role

The Regulatory Operations Specialist plays an essential role to achieve and maintain compliance and business continuity for our existing portfolio of medical devices across the whole product lifecycle, whilst also ensuring we are an effective, well-connected organisation.

Your responsibilities

Supporting post launch regulatory activities for all planned and unplanned compliance and maintenance activities for our medical device portfolio across all markets

Ensuring regulatory changes are implemented within our registration files on a global basis working on collaboration with regional RAS teams, RAS strategy teams and global cross functional partners (which include R&D, procurement, sustainability, supply, quality and any other department where regulatory support is required) with a right first time approach.

Ensuring both planned and unplanned maintenance activities e.g. renewals are completed in a timely manner to ensure business continuity

Driving efficiencies and operational excellence within RAS, align on priorities and resourcing with the Regulatory Operations Team.

Ensuring that you work according to internal and external standards, to ensure our products are compliant according to regulations and internal standards

Managing a complex and diverse set of regulatory requirements and landscape overview across multiple markets

Ensuring regulatory information on various systems and databases are kept up to date

The experience we're looking for Prior experience in Medical Devices or an equivalent regulatory classification is preferred

An ability to work on multiple projects at any given time and a capability to work with the line manager to prioritise and manage workload

You have the knowledge and understanding of regulatory requirements associated with Reckitt products. Medical Device experience is a benefit but not a requirement  You have high scientific credentials with a Bachelor of Science (BSc) / Master of Science (MS) degree in a relevant scientific discipline – such as Chemistry, Biological Sciences, Microbiology, Pharmacy, or significant applied industry experience

You have an ability to deliver to time, cost and quality standards in a fast paced, high-pressure environment

You have a strong collaborative mindset and able to form strong partnerships with cross functional teams

You have a basic understanding how to translate complex regulatory information into a compelling stakeholder friendly language.

You strive for a high level of accuracy in authoring documentation, with a focus on ensuring the level of registered information is appropriate in the dossiers

The skills for success

Task Execution Under Pressure, Business Acumen, Commercial Awareness, Objective Setting, Accountability, Consumer Insight,…
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