Formulation Development Scientist
Posted on Jun 25, 2026 by CV-Library
Ruislip, Greater London, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Full-Time
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
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
Reference: 224958943
https://jobs.careeraddict.com/post/113462523
Formulation Development Scientist
Posted on Jun 25, 2026 by CV-Library
Ruislip, Greater London, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Full-Time
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
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
Reference: 224958943
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