Overview
We are looking for a skilled and driven Formulation Development Scientist to join our UK manufacturing site. This role acts as the critical technical bridge between our India-based R&D center and the UK Technology Transfer (TT) department, supporting the seamless transition of liquid products from development through to commercial manufacturing.
Responsibilities
- Lead and support pilot batch manufacturing, scale-up batches, and troubleshooting of commercial batch failures at the UK site.
- Serve as the primary technical liaison between the India R&D team and the UK TT department, ensuring effective knowledge transfer and alignment on formulation strategies.
- Execute and oversee technology transfer activities for oral liquid and suspension products, ensuring compliance with regulatory requirements and internal quality standards.
- Develop and optimize homogenisation processes for large-volume liquid products, ensuring product uniformity, stability, and consistency at scale.
- Prepare and review technical documents including batch manufacturing records, technology transfer reports, process descriptions, and deviation investigations.
- Identify root causes of manufacturing issues and implement robust corrective and preventive actions (CAPAs).
- Collaborate cross-functionally with QA, QC, Regulatory Affairs, and Manufacturing teams to support product lifecycle activities.
- Contribute to process validation, equipment qualification, and process analytical technology (PAT) initiatives as applicable.
- Stay current with regulatory guidelines (ICH, MHRA, EMA) relevant to liquid dosage form development and manufacturing.
Qualifications & Experience
Education
- M.Pharm / M.Sc. in Pharmaceutics, Pharmaceutical Sciences, or a closely related discipline.
- Ph.D. is an advantage but not mandatory.
Experience
- 6-12 years of hands-on experience in pharmaceutical formulation development, with a focus on oral liquids and suspensions.
- Demonstrated experience in scale-up and technology transfer of liquid dosage forms.
- Practical experience with homogenisation equipment (high-shear mixers, rotor-stator homogenisers) at pilot and commercial scale.
- Prior exposure to a cross-site or cross-functional TT role is highly desirable.
Technical Skills
- Strong understanding of formulation principles for oral liquids and suspensions (rheology, particle size, physicochemical stability).
- Familiarity with ICH Q8/Q9/Q10 guidelines and QbD principles.
- Experience with GMP manufacturing environments and documentation practices.
- Working knowledge of relevant regulatory frameworks (MHRA, EMA, ANDA/CTD as applicable).
Soft Skills
- Strong communication skills — able to operate effectively across geographies and functions.
- Analytical and structured problem-solving mindset.
- Self-driven with the ability to manage multiple priorities independently.
- Collaborative team player with a proactive approach.
Benefits
- A technically stimulating role at the interface of R&D and commercial manufacturing.
- Opportunity to work across international sites with a high-calibre scientific team.
- Competitive salary and benefits package in line with UK industry standards.
#J-18808-Ljbffr