Regulatory Affairs Associate

Role overview

Hlx Life Sciences is seeking a seasoned Regulatory Affairs professional to contribute to EU and UK regulatory submissions, maintain compliance standards, and support broader regulatory strategy across the product range.

Key responsibilities

• Handle regulatory filings and ongoing lifecycle regulatory activities.
• Assess CTD documentation and coordinate communication with health authorities.
• Maintain compliance for marketing authorisations.
• Guide and support junior colleagues within the team.

Requirements

• BSc qualification in Life Sciences, Pharmacy, or Chemistry.
• At least 5 years of experience in pharmaceutical regulatory affairs.
• Solid working knowledge of EU and UK regulatory frameworks, including CTD.
• CMC exposure is preferred, though not mandatory.
• Strong written and verbal communication abilities.
• Good organisational skills and attention to detail.

Additional information

This role is based in the London Area, United Kingdom, and is offered on a part-time, onsite basis.

No salary, stipend, opening count, start date, or application deadline was specified.

No separate perks, eligibility notes, or extra terms were provided.