About this role

We are looking for an experienced professional to join our Research & Development team and drive our research initiatives. This is a high-impact role offering the chance to take on significant responsibility and deepen your expertise in life sciences.

Responsibilities

• Prepare and review SOPs, protocols, and technical reports
• Participate in team meetings, project reviews, and continuous improvement initiatives
• Contribute to regulatory submissions and responses to agency queries
• Collaborate with cross-functional teams on project planning and execution
• Manage budgets, timelines, and vendor relationships for major programs
• Drive regulatory strategy and manage complex submissions across multiple markets
• Apply expertise in Stability Studies, HPLC to deliver high-quality work products

Required qualifications

• 3–5 years of experience in laboratory research, pharmaceutical development, clinical research, or a related life-science role
• Bachelor's degree in Biology, Chemistry, Biochemistry, Pharmacy, Biomedical Engineering, or a related life-science field; Master's degree preferred
• Strong proficiency in Drug Delivery, Excipient Selection, Stability Studies, GMP
• Proven track record of delivering projects on time and within scope
• Excellent communication and collaboration skills
• Excellent written and verbal communication skills in English
• Right to work in the UK

Preferred qualifications

• Prior experience with FDA, EMA, or MHRA regulatory submissions
• Experience in autoimmune disease, immunology, or oncology therapeutic areas
• Experience in medical-device or combination-product regulatory pathways
• Experience with electronic lab notebooks (ELN) and LIMS
• PhD or advanced degree in a relevant scientific discipline
• Arabic or French language skills (for potential MENA operations)