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Senior Regulatory Specialist

External
ecolab logoEcolab · United Kingdom
Full-timeHybridToday
ComplianceExcelSAFe
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Requirements

  • Experience (minimum 2 years) of being in a similar position in the pharmaceutical industry or at health authorities
  • Good knowledge of applicable pharmaceutical regulations - preferably with UK & EU registration procedures
  • Basic knowledge of related ethical code of practice required for GXP compliance
  • Strong written and verbal communication and organizational skills
  • Ability to work independently and collaborate effectively with cross-functional colleagues at all levels of the organization.
  • Ability to multi-task and prioritize work.
  • Fluency in English (speaking, reading, and writing)
  • Proficiency in Microsoft applications (Excel, Word, PowerPoint)
  • About Ecolab:
  • Ecolab's commitment to diversity, equity and inclusion (DE&I) reflects our longstanding value of working together to integrate diverse perspectives to challenge ourselves, reach our goals and do what's right.
  • Apply today and join one of the most ethical companies with over a hundred years of history.
  • Join Ecolab and help us protect what's vital.
  • #li-eu

Benefits

Health insuranceVision insuranceEquity / stock options

Additional Information

In this role you will be supporting the Regulatory Affairs Healthcare Team with implementation, execution and management of pharmaceutical regulatory activities in UK and further European regions, ensuring compliance and growth of our medicinal product portfolio. The position could be based in our Ecolab Ltd. (Northwich) or near our Offices in Caerphilly or Baglan - hybrid working model optional. How you'll make an impact: This position contains tasks related to pharmaceutical regulatory area. Support Cross-Functional European Projects to drive innovation and efficacy Manage diverse maintenance activities of Medicinal Product Licenses (e.g., UK, IE) and export market, like: Preparation and submission of variations Creation and revision of packaging & promotional materials Update of internal and official databases Support audits & inspections Support the Pharmacovigilance system Monitor regulatory/pharmaceutical regulations for the relevant therapeutic areas and share information internally Assist other functions, like customer service and tender business with regulatory expertise Education: Bachelor's degree or equivalent, preferably in life sciences (pharmacy, biology, or similar).


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