Regulatory Operations Specialist - Medical Devices (Kingston upon Hull, East Yorkshire, GB, HU1 1AA)

Reckitt
United Kingdom
Workplace: OnsiteFull timeFunction: Quality & Regulatory (Non-Software)Education: mastersSkills: ["Accountability","Collaboration","Objective setting","Commercial awareness","Business acumen"]

Own post-launch regulatory operations for a global portfolio of medical devices across the full lifecycle. Maintain compliance by implementing regulatory changes in registration files, completing timely planned and unplanned maintenance (e.g., renewals), and keeping regulatory information up to date in internal systems. Partner with regional and global RAS teams and cross-functional stakeholders to drive right-first-time execution, operational efficiencies, and business continuity across multiple markets.

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Reckitt
Reckitt
6 hours ago

Regulatory Operations Specialist - Medical Devices (Kingston upon Hull, East Yorkshire, GB, HU1 1AA)

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Last checked: 6 hours agoStatus: Live

Job Summary

Own post-launch regulatory operations for a global portfolio of medical devices across the full lifecycle. Maintain compliance by implementing regulatory changes in registration files, completing timely planned and unplanned maintenance (e.g., renewals), and keeping regulatory information up to date in internal systems. Partner with regional and global RAS teams and cross-functional stakeholders to drive right-first-time execution, operational efficiencies, and business continuity across multiple markets.
Location: United Kingdom
Workplace: Onsite
Employment Type: Full time
Job Function: Quality & Regulatory (Non-Software)

Key Responsibilities

  • •Support post-launch regulatory activities for planned and unplanned compliance and maintenance across the medical device portfolio in all markets.
  • •Implement regulatory changes within registration files globally in collaboration with regional RAS, RAS strategy, and cross-functional partners.
  • •Ensure planned and unplanned maintenance activities (e.g., renewals) are completed on time to support business continuity.
  • •Drive efficiencies and operational excellence within RAS by aligning on priorities and resourcing with the Regulatory Operations Team.
  • •Manage regulatory requirements and maintain up-to-date regulatory information in relevant systems and databases.

Pay and Benefits

Perks:Parental BenefitsEmployee AssistanceLife InsuranceShare Plans

Key Requirements

  • •Prior experience in Medical Devices or an equivalent regulatory classification is preferred.
  • •Knowledge of regulatory requirements associated with the company’s products; medical device experience is a benefit but not required.
  • •High scientific credentials with a Bachelor of Science (BSc) / Master of Science (MS) in a relevant scientific discipline (e.g., Chemistry, Biological Sciences, Microbiology, Pharmacy) or significant applied industry experience.
  • •Ability to manage multiple projects and prioritise workload with the line manager in a fast-paced environment.
  • •High accuracy in authoring documentation, ensuring registered information is appropriate in the dossiers.
Education:Master's in Relevant scientific discipline (e.g., Chemistry, Biological Sciences, Microbiology, Pharmacy)
Skills:AccountabilityCollaborationObjective settingCommercial awarenessBusiness acumen

Company Brief

Reckitt
Global consumer goods company producing health, hygiene, and home products across well-known brands. Operates in multiple markets offering over-the-counter health, personal care, and household cleaning products to consumers worldwide.
Industry: FMCG
Company Size: Enterprise (1,001+ employees)
Revenue: USD 1B+
Growth: Public Company
Valuation: Public Company (Market Cap in USD)
Funding: IPO / Publicly Listed
Headquarters: Slough, United Kingdom
Founded: 1999
WebsiteLinkedIn