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Senior Formulation Scientist

Job in Leeds, West Yorkshire, ME17, England, UK
Listing for: Rosemont Pharmaceuticals
Full Time position
Listed on 2026-09-01
Job specializations:
  • Pharmaceutical
    Pharmaceutical Science/ Research, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 65000 - 90000 GBP Yearly GBP 65000.00 90000.00 YEAR
Job Description & How to Apply Below

For over 50 years, Rosemont Pharmaceuticals has been a trusted name in the development and manufacture of oral liquid medicines. With a portfolio of over 130 products - including 70 licensed medicines - we’re proud to support healthcare professionals and patients, especially those with swallowing difficulties.

Our purpose is clear: to improve patient outcomes through innovation in liquid formulations. We’re highly respected across the pharmaceutical industry and have played a key role in establishing best practices for dysphagia care.

Our mission is to create a globally connected, people-focused organisation where every individual is empowered to thrive and achieve their best. If you're passionate about making a meaningful impact to patients across the world and want to be part of a company with a strong heritage and ambitious vision, we’d love to hear from you.

About the Role

We are seeking an experienced Senior Formulation Scientist to join our Research & Development team. This is an exciting opportunity to play a key role in developing innovative, patient-focused pharmaceutical formulations that support Rosemont’s mission of improving patient outcomes.

Reporting to the Formulation & Innovation Manager, you will lead the development of robust and stable formulations from concept through to commercialisation, applying your scientific expertise to create high-quality products that meet regulatory, commercial, and patient needs across the UK, Europe, and United States.

This role required the successful candidate to be based at out Leeds facility Monday – Friday each week.

Key Responsibilities
  • Independently develop robust, stable, and patient-focused oral pharmaceutical formulations.
  • Design and optimise formulations and manufacturing processes for new product development.
  • Manage multiple development projects from early-stage approval through to scale-up and regulatory submission.
  • Support the introduction of new products through cross-functional collaboration and project participation.
  • Produce manufacturing methods and support technical transfer into commercial production.
  • Develop protocols, reports, and validation documentation to support product development activities.
  • Ensure stability programmes and regulatory requirements are fully met.
  • Collaborate with Analytical Development teams to support analytical method development, validation, and transfer.
  • Maintain accurate scientific records and documentation in compliance with internal procedures.
  • Produce and review scientific documentation including SOPs, work instructions, protocols, reports, and COSHH assessments.
  • Identify opportunities to improve products, processes, and development systems.
  • Remain informed of emerging scientific developments and promote best practice across the business.
  • Ensure all activities comply with GLP, cGMP, and relevant quality standards.
What We're Looking For:
  • Master's degree in Pharmaceutical Technology, Pharmaceutics, or a related scientific discipline.
  • Multiple years experience in a laboratory-based formulation development role.
  • Experience with in the generic pharmaceutical industry.
  • Strong experience developing and optimising formulations from concept through to commercial launch.
  • Experience working within UK/EU and US pharmaceutical regulatory environments.
  • Strong understanding of GMP requirements.
  • Strong analytical and problem-solving abilities with a data-driven approach.
  • Excellent written and verbal communication skills, with the ability to engage confidently with stakeholders.
Technical Expertise
  • Proven experience developing sustained-release and modified-release oral formulations.
  • Strong knowledge of polymers used in oral sustained-release dosage forms.
  • Hands-on experience with ion-exchange resin complexation technologies.
  • Hands-on experience with particle coating technologies.
  • Experience with hot-melt granulation would be advantageous.
Personal Attributes
  • Demonstrates integrity, accountability, and professionalism.
  • Builds strong working relationships and collaborates effectively across teams.
  • Continuously seeks opportunities to learn, develop, and share knowledge.
  • Customer-focused with an understanding of both internal and external…
Position Requirements
10+ Years work experience
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