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

Reckitt
United Kingdom
Workplace: OnsiteContractFunction: Quality & Regulatory (Non-Software)Education: mastersSkills: ["Collaboration","Accuracy","Accountability","Communication","Prioritization"]

Support end-to-end medicinal regulatory operations by maintaining high-quality variation packages, ensuring accurate dossier content, and maintaining compliance across the full product lifecycle. Deliver high-quality submissions to agreed timeframes while collaborating with cross-functional teams including RAS Global, Medical, R&D, Supply, Quality, and Marketing. Maintain GMP documentation support for medicinal manufacturing sites and stay current with evolving global regulations and best practices.

Loading

Loading job details...

Preparing the role view and application actions.

FursaFursa
Reckitt
Reckitt
1 day ago

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

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI
Last checked: 17 hours agoStatus: Live

Job Summary

Support end-to-end medicinal regulatory operations by maintaining high-quality variation packages, ensuring accurate dossier content, and maintaining compliance across the full product lifecycle. Deliver high-quality submissions to agreed timeframes while collaborating with cross-functional teams including RAS Global, Medical, R&D, Supply, Quality, and Marketing. Maintain GMP documentation support for medicinal manufacturing sites and stay current with evolving global regulations and best practices.
Location: United Kingdom
Workplace: Onsite
Employment Type: Contract
Job Function: Quality & Regulatory (Non-Software)
Seniority: Mid level

Key Responsibilities

  • •Support medicinal regulatory requirements and maintain dossier and compliance activities across multiple markets post-launch.
  • •Deliver high quality submissions within agreed operational timeframes in collaboration with partner functions.
  • •Provide non-dossier maintenance support, including GMP documentation support for medicinal manufacturing sites globally.
  • •Ensure activities follow the operating model and internal best practices, using systems compliantly for audit readiness.
  • •Maintain compliance throughout the product lifecycle post approval and apply relevant updates from an ever-changing regulatory environment.

Pay and Benefits

Perks:Parental LeaveLife Insurance

Key Requirements

  • •Prior experience in regulatory affairs, including knowledge of 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.
  • •Ability to manage multiple projects, prioritise workload independently and collaborate as part of a team.
  • •Scientific credentials with a Bachelor of Science (BSc) or Master of Science (MS) in a relevant discipline (e.g., Chemistry, Biological Sciences, Microbiology, Pharmacy).
Experience:Regulatory affairsPharmaceuticals
Education:Master's in Chemistry, Biological Sciences, Microbiology, Pharmacy (or other relevant scientific discipline)
Skills:CollaborationAccuracyAccountabilityCommunicationPrioritization

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