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

Reckitt
United Kingdom
Workplace: OnsiteFull timeFunction: Quality & Regulatory (Non-Software)Education: bachelorsSkills: ["Collaboration","Accountability","Accuracy","Stakeholder communication","Prioritisation"]

Ensure high-quality regulatory dossier and variation-package maintenance across medicinal regulations worldwide. Own consistent, timely regulatory dossier activities throughout the product lifecycle, supporting post-launch compliance and audit readiness. Collaborate with cross-functional partners across RAS Global, Medical, R&D, Supply, Quality, and Marketing, including non-dossier maintenance support such as GMP documentation. Manage multiple regulatory requirements across markets while meeting operations deadlines with high accuracy.

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Reckitt
Reckitt
1 day ago

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

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Last checked: 17 hours agoStatus: Live

Job Summary

Ensure high-quality regulatory dossier and variation-package maintenance across medicinal regulations worldwide. Own consistent, timely regulatory dossier activities throughout the product lifecycle, supporting post-launch compliance and audit readiness. Collaborate with cross-functional partners across RAS Global, Medical, R&D, Supply, Quality, and Marketing, including non-dossier maintenance support such as GMP documentation. Manage multiple regulatory requirements across markets while meeting operations deadlines with high accuracy.
Location: United Kingdom
Workplace: Onsite
Employment Type: Full time
Job Function: Quality & Regulatory (Non-Software)

Key Responsibilities

  • •Support regulatory dossier maintenance and compliance post-launch across multiple markets by maintaining appropriate detail for internal use and ongoing maintenance.
  • •Ensure high-quality submission delivery within agreed operational timeframes through collaboration with partner functions.
  • •Support non-dossier maintenance activities, including GMP documentation support for medicinal manufacturing sites.
  • •Maintain compliant use of internal systems and processes to ensure audit readiness at all times.
  • •Monitor and apply changes in the regulatory environment to product and dossier updates while meeting business/project deadlines.

Pay and Benefits

Perks:Parental LeaveHealth InsuranceLife Insurance

Key Requirements

  • •Prior experience in regulatory affairs, including dossier creation and global registrations.
  • •Knowledge of regional and global regulatory environments and how they impact dossiers and registrations.
  • •Experience preparing and submitting dossiers for medicinal registrations and supporting documentation.
  • •Capability to manage multiple projects, prioritise independently and as part of a wider team.
  • •Scientific credentials with a Bachelor of Science or Master of Science in a relevant discipline (e.g., Chemistry, Biological Sciences, Microbiology, Pharmacy).
Education:Bachelor's
Skills:CollaborationAccountabilityAccuracyStakeholder communicationPrioritisation

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