* UK + Ireland Regulatory Affairs Officer
* West Berkshire, UK – Hybrid, 3x a week on site
* Salary up to £50,000 + benefits
3 to 5 years of prior UK + Ireland market experience in Regulatory Affairs
Cpl Life Sciences is partnering with a well-established pharmaceutical organisation who are seeking someone who is passionate about improving healthcare and ensuring the safety and effectiveness of medicines.
They are seeking a well-established UK & Ireland Regulatory Affairs Officer to join the team to help obtain, manage, and maintain product Marketing Authorisations across the UK and Ireland—supporting both new and established medicines. You’ll work collaboratively with cross‑functional teams and contribute to impactful regulatory projects that shape the future of healthcare.
Key Responsibilities
* Co‑ordinate, prepare and submit high‑quality registration applications to UK and/or Irish Regulatory Authorities, ensuring Marketing Authorisations are secured and maintained in line with business goals.
* Support the preparation, distribution and tracking of regulatory documentation for UK and Ireland submissions.
* Ensure all data submitted meets the highest scientific and presentation standards, while adhering to deadlines.
* Work proactively with global business units and functional teams to meet project requirements compliantly and on time.
* Assist in developing local registration strategies and contribute to operational planning for product commercialisation.
* Play an active role in departmental and cross‑functional project teams.
* Support regulatory activities across the full product lifecycle, including variations, renewals and notifications.
* Provide regulatory insight, with guidance, into commercial and brand planning discussions.
About You
* Previous experience in Regulatory Affairs within the pharmaceutical industry.
* Prior UK & Ireland submissions experience absolutely essential.
* Degree in Life Sciences, Chemistry, or equivalent relevant experience.
* Strong understanding of pharmaceutical R&D processes and ability to interpret scientific data across disciplines.
* Capable of working across multiple therapeutic areas and representing Regulatory Affairs in brand discussions (with managerial support).
* Awareness of EU procedures for Marketing Authorisations and submissions.
* Knowledge of lifecycle management, including variations, renewals, and Health Authority notification processes.
* Highly organised with excellent attention to detail, and strong written and verbal communication skills.
* Confident working cross‑functionally and building relationships with internal teams.
What’s in It for You?
* The opportunity to contribute to meaningful, science‑driven work that improves lives worldwide.
* A supportive, forward‑thinking environment that encourages personal and professional growth.
* Opportunities for career development locally or internationally.
* A competitive, thoughtfully designed rewards package that recognises your impact.
* Comprehensive health and wellbeing benefits, including high‑quality healthcare, wellness programmes, and at least 14 weeks of gender‑neutral parental leave.
Please note that there is limited flexible around the 3x a week hybrid working policy and all individuals are expected to honour this policy.
For more information, please contact lucy.kirkaldy@cpl.com