Regulatory Operations Specialist, Medicines (12-Month FTC)

Reckitt
United Kingdom
Workplace: OnsiteContractFunction: Quality & Regulatory (Non-Software)Education: mastersSkills: ["Accountability","Collaboration","Commercial awareness","Business acumen","Attention to detail"]

Own the end-to-end regulatory operations activities for medicinal variation packages, ensuring dossiers and submissions are completed with appropriate detail, consistency, and compliance throughout the product lifecycle. Maintain regulatory readiness by applying best practices and compliant system usage, and support ongoing dossier maintenance and GMP documentation support across Reckitt’s medicinal manufacturing sites. Partner with global cross-functional stakeholders to deliver high-quality information on time and keep products compliant across evolving regulations.

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Reckitt
Reckitt
2 hours ago

Regulatory Operations Specialist, Medicines (12-Month FTC)

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Last checked: 2 hours agoStatus: Live

Job Summary

Own the end-to-end regulatory operations activities for medicinal variation packages, ensuring dossiers and submissions are completed with appropriate detail, consistency, and compliance throughout the product lifecycle. Maintain regulatory readiness by applying best practices and compliant system usage, and support ongoing dossier maintenance and GMP documentation support across Reckitt’s medicinal manufacturing sites. Partner with global cross-functional stakeholders to deliver high-quality information on time and keep products compliant across evolving regulations.
Location: United Kingdom
Workplace: Onsite
Employment Type: Contract · 12 months
Job Function: Quality & Regulatory (Non-Software)

Key Responsibilities

  • •Support a complex set of regulatory requirements to enable dossier maintenance and compliance after launch across multiple markets.
  • •Deliver high-quality regulatory submissions within agreed operations time frames and coordinate across partner functions to ensure timely information.
  • •Support non-dossier maintenance activities, including GMP documentation support for Reckitt medicinal manufacturing sites globally.
  • •Ensure all activities follow the operating model and internal best practice, including compliant use of systems for audit readiness.
  • •Maintain compliance during the product lifecycle post approval and apply relevant updates as the regulatory environment changes.

Pay and Benefits

Equity and Bonus:Equity
Perks:Parental LeaveEmployee AssistanceLife InsuranceEquity

Key Requirements

  • •Experience in regulatory affairs with knowledge of dossier creation and global registrations.
  • •Knowledge of regional and global regulatory environments and how they affect regulatory dossiers and registrations.
  • •Experience preparing and submitting dossiers for medicinal registrations and supporting documentation.
  • •Ability to manage multiple projects, prioritize workload, and work independently and collaboratively.
  • •Scientific credentials with a Bachelor of Science (BSc) or Master of Science (MS) in a relevant field such as Chemistry, Biological Sciences, Microbiology, or Pharmacy.
Education:Master's in Chemistry, Biological Sciences, Microbiology, Pharmacy (or other relevant scientific discipline)
Skills:AccountabilityCollaborationCommercial awarenessBusiness acumenAttention to detail

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