Job Description
The Role:
* You will organise and manage scientific research to support regulatory objectives, method development and product optimisation. Working closely with cross-functional teams including Regulatory Affairs, QA and QC, you will ensure robust, compliant and scientifically sound data delivery.
* This is a role for someone who can think critically, communicate clearly and operate both independently and within collaborative project teams.
Key Responsibilities:
* Lead and manage multiple scientific development projects within Chemistry, Biochemistry or Immunology-related disciplines
* Develop and validate analytical methods in line with current regulatory requirements
* Interpret experimental data and prepare documentation for regulatory submissions and technical dossiers
* Provide scientific support to internal stakeholders including Regulatory Affairs, QA, QC and Commercial teams
* Ensure projects are delivered to agreed timelines, maintaining strong communication with stakeholders
* Maintain compliance with GMP and relevant regulatory guidance (ICH, USP, EudraLex)
* Contribute to continuous improvement initiatives within laboratory processes and systems
* Communicate scientific findings internally and, where appropriate, at conferences or seminars
* Maintain clear, traceable documentation in line with quality standards
What We’re Looking For:
Essential:
* BSc in Chemistry, Biochemistry, or related discipline
* 2+ years’ experience within a pharmaceutical or biotechnology environment
* Experience developing and validating analytical methods
* Understanding of regulatory guidance (ICH, USP, EudraLex)
* Strong data interpretation and documentation skills
Desirable:
* PhD in a relevant scientific discipline
* 3+ years’ industry experience
* Experience contributing to regulatory submissions
* Membership of a relevant professional body