Lead Pharmaceutical Formulation Scientist
- cardiff, wales, CF10, United Kingdom
- Permanent·On-site
- Full time
- £70,000 - £70,000 Per Annum
Job Description
About the Role
Our client seeks a dynamic and innovative Lead Pharmaceutical Formulation Scientist to spearhead drug formulation development in their state-of-the-art facility in Cardiff . This senior role involves leading a team of scientists in designing, developing, and optimising novel drug delivery systems and pharmaceutical formulations. You will play a critical role in advancing pipeline projects from early-stage research through to clinical development, ensuring the efficacy, safety, and manufacturability of new medicines. This is a fantastic opportunity for an experienced formulation scientist looking to make a significant impact in a challenging and rewarding environment.
Key Responsibilities
- Lead and mentor a team of formulation scientists, overseeing day-to-day laboratory activities and project progress.
- Design and execute formulation development studies for various dosage forms (e.g., tablets, capsules, injectables, topicals).
- Conduct pre-formulation characterisation, stability studies, and physicochemical assessments of drug substances and formulations.
- Optimise formulations to enhance bioavailability, stability, and patient compliance, while ensuring scalability for manufacturing.
- Prepare comprehensive development reports, technical summaries, and contribute to regulatory submissions.
- Collaborate closely with process development, analytical development, and manufacturing teams to ensure seamless technology transfer.
Requirements
- PhD or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related field.
- Minimum of 7 years of progressive experience in pharmaceutical formulation development, with a proven track record of successfully advancing projects.
- In-depth knowledge of drug delivery technologies, excipient science, and various dosage form development.
- Experience in leading scientific teams and managing project timelines effectively.
- Familiarity with GMP requirements and regulatory guidelines relevant to drug product development.
- Excellent analytical, problem-solving, and critical thinking skills, with strong report writing capabilities.
Benefits
- Highly competitive salary and comprehensive bonus structure.
- On-site role within a cutting-edge pharmaceutical research centre.
- Extensive healthcare benefits, including private medical insurance and wellness programmes.
- Contributory pension scheme and life insurance.
- Significant opportunities for leadership development and scientific advancement.


