Senior Regulatory Specialist in Cardiff

Senior Regulatory Specialist in Cardiff

Cardiff Full-Time 40000 - 50000 £ / year (est.) No working from home possible
Ecolab

At a Glance

  • Tasks: Support regulatory activities in the pharmaceutical sector and ensure compliance across Europe.
  • Company: Join Ecolab, a leader in healthcare innovation with a commitment to inclusion.
  • Benefits: Hybrid working model, competitive salary, and opportunities for professional growth.
  • Other info: Collaborative environment with a focus on diversity and career advancement.
  • Why this job: Make a real impact on healthcare by driving regulatory excellence and innovation.
  • Qualifications: Bachelor’s degree in life sciences and two years of relevant experience required.

The predicted salary is between 40000 - 50000 £ per year.

In this role you will be supporting the Regulatory Affairs Healthcare Team with implementation, execution and management of pharmaceutical regulatory activities in the 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 – a hybrid working model is optional.

  • How You’ll Make An Impact
  • Support cross‑functional European projects to drive innovation and efficacy.
  • Manage diverse maintenance activities of medicinal product licences, including UK and IE and export markets.
  • Preparation and submission of variations.
  • Creation and revision of packaging and promotional materials.
  • Update of internal and official databases.
  • Support audits and inspections.
  • Support the pharmacovigilance system.
  • Monitor regulatory and pharmaceutical regulations for the relevant therapeutic areas and share information internally.
  • Assist other functions, such as customer service and tender business, with regulatory expertise.

Education

  • Bachelor’s degree or equivalent, preferably in life sciences (pharmacy, biology, or similar).

Qualifications

  • Minimum two years of experience in a similar position in the pharmaceutical industry or at health authorities.
  • Good knowledge of applicable pharmaceutical regulations – preferably with UK and EU registration procedures.
  • Basic knowledge of related ethical code of practice required for GXP compliance.
  • Strong written and verbal communication and organisational skills.
  • Ability to work independently and collaborate effectively with cross‑functional colleagues at all levels.
  • Ability to multi‑task and prioritise work.
  • Fluency in English (speaking, reading and writing).
  • Proficiency in Microsoft Office applications (Excel, Word, Power Point).
  • Our Commitment to a Culture of Inclusion & Belonging

Ecolab is committed to fair and equal treatment of associates and applicants and furthering the principles of Equal Opportunity to Employment.

We will recruit, hire, promote, transfer and provide opportunities for advancement based on individual qualifications and job performance in all matters affecting employment, compensation, benefits, working conditions, and opportunities for advancement.

Ecolab will not discriminate against any associate or applicant for employment because of race, religion, colour, creed, national origin, citizenship status, sex, sexual orientation, gender identity and expression, genetic information, marital status, age, or disability.

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Ecolab

Contact Details:

Ecolab Recruitment Team

We think you need these skills to ace Senior Regulatory Specialist in Cardiff

Regulatory Affairs
Pharmaceutical Regulations
UK and EU Registration Procedures
GXP Compliance
Cross-Functional Collaboration
Project Management
Communication Skills