2,059 Formulation Development jobs in the United Kingdom

Senior Formulation Development Scientist

Upperton Pharma Solutions is a Nottingham-based CDMO that specialises in the development and manufacture of pharmaceutical products, providing a complete service from early-stage feasibility to GMP clinical manufacture. Formulations cover a range of delivery routes, typically including oral (tablets & capsules), nasal, inhaled and sterile products.

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• Lead the formulation development of new drug candidates, including pre-formulation studies, excipient screening, and dosage form design.
• Develop and optimize formulations for various routes of administration (e.g., oral, injectable, topical).
• Conduct stability studies and establish appropriate storage conditions and shelf-life for drug products.
• Utilize advanced analytical techniques to characterize drug substances and drug products.
• Troubleshoot formulation-related issues and provide scientific guidance to development teams.
• Design and execute studies for technology transfer to manufacturing sites.
• Prepare and review formulation development reports, regulatory submission documents (e.g., IND, NDA), and scientific publications.
• Stay abreast of current trends and advancements in pharmaceutical formulation science and drug delivery technologies.
• Mentor junior scientists and provide technical leadership within the R&D department.
• Collaborate effectively with cross-functional teams, including analytical development, DMPK, CMC, and regulatory affairs.
• Manage external collaborations with CROs and academic institutions as needed.

• PhD in Pharmaceutical Sciences, Pharmaceutics, Chemistry, Chemical Engineering, or a related field.
• Minimum of 7 years of experience in pharmaceutical formulation development, with a focus on small molecules or biologics.
• In-depth knowledge of formulation principles, excipient functionality, and drug delivery technologies.
• Experience with various analytical techniques (e.g., HPLC, GC, DSC, TGA, dissolution testing).
• Proficiency in designing and conducting stability studies.
• Strong understanding of regulatory requirements (e.g., FDA, EMA) for drug development.
• Excellent leadership, communication, and interpersonal skills.
• Proven ability to manage projects and mentor scientific staff.
• Experience with solid dosage forms, parenteral formulations, or other advanced delivery systems is highly desirable.

• Lead and execute formulation development projects for novel and generic drug products, focusing on solid oral dosage forms, injectables, or other relevant modalities.
• Conduct pre-formulation studies to characterize active pharmaceutical ingredients (APIs) and excipients.
• Design and optimize formulations to achieve desired drug release profiles, stability, and bioavailability.
• Develop and validate analytical methods for characterizing formulations and APIs.
• Plan and execute experiments to support formulation scale-up and technology transfer to manufacturing.
• Prepare comprehensive technical reports, development summaries, and regulatory submission documents (e.g., IND, NDA).
• Collaborate closely with analytical development, process chemistry, manufacturing, and regulatory affairs teams.
• Stay abreast of the latest advancements in pharmaceutical formulation science, drug delivery technologies, and regulatory guidelines.
• Troubleshoot formulation and process-related issues encountered during development and manufacturing.
• Manage project timelines, resources, and budgets effectively.
• Mentor junior scientists and provide technical guidance.
• Contribute to the intellectual property strategy through patentable inventions.
• Ensure all laboratory activities comply with Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) standards.
• Present research findings at internal meetings and external scientific conferences.
• Evaluate and recommend new technologies and equipment for formulation development.

• PhD or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related discipline.
• Minimum of 5 years of relevant experience in pharmaceutical formulation development within the industry.
• Proven track record of successfully developing and characterizing various dosage forms.
• Hands-on experience with techniques such as granulation, tableting, encapsulation, lyophilization, or sterile product manufacturing.
• Strong understanding of API characterization, excipient functionality, and drug-excipient compatibility.
• Proficiency in relevant analytical techniques (e.g., HPLC, dissolution testing, DSC, TGA).
• Knowledge of regulatory requirements for drug development (e.g., FDA, EMA guidelines).
• Excellent scientific writing, presentation, and communication skills.
• Strong problem-solving abilities and a meticulous attention to detail.
• Experience with project management and leading cross-functional teams is a plus.
• Ability to work independently and collaboratively in a dynamic R&D environment.

• Lead the design and development of innovative pharmaceutical formulations.
• Conduct pre-formulation studies, solubility enhancement, and excipient compatibility assessments.
• Develop and optimize solid, liquid, and other dosage forms.
• Plan and execute scale-up activities and technology transfer to manufacturing.
• Design and manage stability studies and interpret data.
• Troubleshoot formulation-related issues and implement solutions.
• Collaborate with cross-functional teams, including analytical, CMC, and regulatory.
• Contribute to regulatory submissions and scientific documentation.
• Mentor and guide junior members of the formulation development team.
• Stay current with scientific literature and emerging formulation technologies.

• PhD or Master's degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related field.
• Minimum of 7 years of progressive experience in pharmaceutical formulation development.
• In-depth knowledge of drug delivery systems, dosage form design, and manufacturing processes.
• Experience with various analytical techniques relevant to formulation characterization.
• Familiarity with GMP regulations and guidelines.
• Strong problem-solving, analytical, and critical thinking skills.
• Excellent written and verbal communication skills for scientific presentations and reports.
• Ability to work effectively in a hybrid team setting and lead scientific projects.

• Lead and execute the formulation development of novel pharmaceutical products, including oral solid dosage forms, injectables, and topical preparations.
• Design and conduct pre-formulation studies, including solubility, stability, and compatibility assessments.
• Develop robust and scalable manufacturing processes for drug products.
• Perform characterisation of raw materials and finished products using various analytical techniques.
• Troubleshoot formulation and process-related issues, implementing effective solutions.
• Write comprehensive development reports, protocols, and regulatory submission documents (e.g., IND, NDA sections).
• Collaborate effectively with cross-functional teams, including analytical development, manufacturing, quality assurance, and regulatory affairs.
• Stay abreast of scientific literature, emerging technologies, and regulatory guidelines relevant to pharmaceutical development.
• Oversee laboratory activities, ensuring compliance with GLP/GMP standards.
• Mentor and guide junior scientists, fostering a culture of scientific rigor and innovation.
• Contribute to strategic planning and pipeline advancement for new drug candidates.

• Ph.D. or Master's degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related discipline.
• A minimum of 6 years of progressive experience in pharmaceutical formulation development.
• In-depth knowledge of drug delivery systems, excipient science, and solid-state chemistry.
• Proven experience with various dosage forms and formulation techniques.
• Familiarity with analytical techniques for drug product characterisation (e.g., HPLC, dissolution testing, DSC, XRD).
• Strong understanding of regulatory requirements (FDA, EMA) and GMP/GLP guidelines.
• Excellent written and verbal communication skills, with the ability to prepare technical documents and reports.
• Demonstrated leadership potential and ability to manage projects independently in a remote setting.
• Proficiency in statistical analysis and experimental design.
• A proactive, results-oriented approach with a commitment to scientific excellence.

Formulation & Product Development Specialist – EU Nutraceuticals

Location: Remote (UK based)

Travel: Occasional EU + China

Comp: Strong base + high-impact bonus

Shape the future of nutraceutical innovation in Europe.

This is your chance to own formulation strategy across Europe for one of the fastest-growing names in nutraceuticals. This is a business in expansion mode - and they need your expertise to lead innovation, win clients, and deliver commercially viable solutions.

You’ll step into a mission-critical role as the go-to EU formulator, advising global clients, collaborating with R&D, and partnering with commercial leaders across the US and APAC.

What’s in it for you

• Impact from day one – take full ownership of EU formulation strategy.
• Global platform – work across 40+ countries with teams in the US, China, and APAC.
• High visibility – senior client-facing role with influence over product direction.
• Premium package – strong base salary, excellent benefits, and international travel opportunities.
• Growth trajectory – join at a pivotal stage as revenues multiply six-fold in the next four years.

Why join?

This is a global health supplement innovator trusted by B2B clients in 40+ countries. Lean, entrepreneurial, and ambitious, they back their people with resources, visibility, and real accountability. Your predecessor spent 30+ years here — proof that this is a role with staying power and long-term impact.

What you’ll be doing

• Lead EU formulation development across categories — efficacy, compliance, market fit
• Partner directly with clients on formulation strategy, positioning, and regulations
• Bring new ideas: spot trends, champion clinically substantiated innovations, and build them into the pipeline
• Connect globally with dosage, R&D, and commercial teams across China, APAC, and the US

Who you are

• Proven B2B supplement formulator (CMO, consultancy, or in-house)
• Deep grasp of EU supplement legislation and regulatory nuance
• Commercially sharp — able to win credibility with customers as both scientist and strategist

Who this suits

You’re not just a formulator. You’re a commercial partner, technical lead, and innovator. You thrive when you’re trusted to own outcomes, not just deliver inputs — and you want the stage to shape the future of formulations at global scale.

Apply now for a confidential conversation with Walker Lovell.