Formulation Development Scientist

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 centre and the UK Technology Transfer (TT) department, supporting the seamless transition of liquid products from development through to commercial manufacturing.

Key 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 optimise 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.

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