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B&S Group (Laxmico Ltd)

Formulation Development Scientist

B&S Group (Laxmico Ltd) Ruislip
32 - 40 hour


Show Recently closed jobs

    B&S Group (Laxmico Ltd)

    Formulation Development Scientist

    B&S Group (Laxmico Ltd) Ruislip
    32 - 40 hour
    Status Open
    Apply now

    Apply on the employer's website


    What we ask

    Education

    No minimum education required

    What we offer

    Hours
    32 to 40 hours per week
    Employment type
    permanent

    Job description

    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 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
    Apply now

    Apply on the employer's website

    Apply now

    Apply on the employer's website


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