Scientist Formulation Development

Scientist Formulation Development

Full-Time 35000 - 45000 £ / year (est.) No working from home possible
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At a Glance

  • Tasks: Design and develop innovative drug formulations while collaborating with a dynamic team.
  • Company: Join a leading European contract manufacturer in the pharmaceutical and biotech sectors.
  • Benefits: Competitive salary, flexible hours, and opportunities for personal and professional growth.
  • Other info: Thriving, fast-paced environment with excellent career advancement opportunities.
  • Why this job: Make a real impact in healthcare by advancing cutting-edge drug formulations.
  • Qualifications: BSc in Pharmaceutical Sciences or related field; experience in formulation development preferred.

The predicted salary is between 35000 - 45000 £ per year.

We are one of the leading European contract manufacturers in the pharmaceutical, biotech and healthcare sectors, with some 2,300 employees in Germany, France, Finland, UK and Norway. For us, the next step is always the one that matters most. Our fast pace drives us forward, fills our working environment with life and spurs our growth. Our winning formula for shared success: room for passion. Because we know that passion is the best medicine when it comes to excellent service around the world. Welcome to NextPharma.

Job Purpose:

Reporting to the Formulation Development Manager, this role offers the opportunity to contribute across three critical areas: clinical manufacturing, development of innovative formulations, and execution of hands‑on laboratory work within the development environment. We are seeking a candidate with a strong pharmaceutical background and a passion for formulation science, ideally with experience working in a cGMP environment within FDA and MHRA-regulated settings. The successful candidate will thrive in a collaborative, fast‑paced environment and play an active role in advancing complex formulations from development through to clinical manufacture. Experience with lipid‑based formulations and/or hot melt extrusion is advantageous.

Key responsibilities and accountabilities:

  • Take ownership of the design and development of formulations and associated manufacturing processes for encapsulated drug products, ensuring alignment with the target product profile and project objectives.
  • Act as a key point of contact for assigned projects, proactively engaging with clients and internal stakeholders to drive progress, resolve challenges, and ensure successful delivery.
  • Lead the planning, design, execution, and reporting of experimental work, ensuring activities are delivered to a high scientific standard and within agreed timelines.
  • Demonstrate accountability for data interpretation and decision‑making, providing clear conclusions and well‑justified recommendations to advance projects.
  • Drive manufacturing process development, including optimisation, scale‑up, and robustness studies to enable successful clinical and commercial manufacture.
  • Take responsibility for the preparation of high‑quality client documentation, including protocols, technical reports, and batch records.
  • Own the delivery of small‑scale GMP manufacture of technical and clinical batches, ensuring compliance with regulatory and quality standards.
  • Play an active role in technology transfer activities, ensuring formulations and processes are successfully translated into commercial manufacturing environments.
  • Provide expert technical support to Manufacturing, leading or contributing to troubleshooting, root cause analysis, and process optimisation initiatives.
  • Contribute to a high‑performing team environment by mentoring and developing less experienced colleagues, fostering engagement, knowledge sharing, and continuous improvement.

Person Profile:

The ideal candidate will:

  • Demonstrate resilience and composure, thriving under pressure and embracing challenges with a proactive, solutions‑focused mindset.
  • Act with integrity and accountability, confidently communicating facts in a clear and constructive manner, building trust with colleagues and clients, and taking ownership of decisions and outcomes — including learning from mistakes.
  • Exhibit sound judgement and decision‑making, drawing on data, experience, and insight to make timely, well‑informed choices that move projects forward.
  • Take ownership of priorities, driving focus on what matters most, effectively managing time and resources while removing barriers to progress and maintaining project momentum.
  • Apply strong analytical thinking and structured problem‑solving skills, using data‑driven approaches to overcome complex challenges and deliver effective, practical solutions.
  • Embrace continuous improvement, actively seeking opportunities to enhance processes, ways of working, and technical approaches.
  • Demonstrate a growth mindset, showing curiosity, openness to feedback, and a commitment to ongoing personal and professional development.
  • Thrive in a dynamic, collaborative, and energised team environment, contributing positively to team culture and bringing enthusiasm to shared goals.

Personal Situation:

Flexible and able to work extended hours when required.

Specific Job Skills:

Required:

  • A minimum of a BSc (or equivalent) in Pharmaceutical Sciences, Chemistry, or a related discipline.
  • Proven experience within the pharmaceutical or biotechnology industry, with a strong understanding of drug development environments.
  • Experience in oral formulation development, preferably including liquid‑filled hard capsules.
  • Demonstrated track record of successfully delivering R&D projects from concept through to completion, with a clear understanding of formulation and drug delivery challenges.
  • Strong written and verbal communication skills in English, with the ability to produce high‑quality technical reports and deliver clear, impactful presentations.
  • A self‑motivated and proactive approach, with the ability to work independently while taking ownership of deliverables.
  • PhD in Pharmaceutical Sciences, Chemistry, or a related discipline.
  • 2+ years’ technical experience in formulation and drug delivery within the pharmaceutical industry.
  • Experience of end‑to‑end product development within a regulated pharmaceutical environment.
  • Expertise in lipid‑based formulations, bioavailability enhancement technologies, and/or advanced drug delivery approaches.
  • A broad, working knowledge of cGMP and GLP environments, with practical experience applying these standards in day‑to‑day activities.

Digital & Data Skills:

  • Proficient in MS Office and modern digital tools, with the ability to analyse, manage, and present data effectively.

Technical Writing & Data Interpretation:

  • Strong scientific writing skills with the ability to interpret and clearly communicate analytical and experimental data.

Communication & Stakeholder Engagement:

  • Confident communicator able to engage effectively with clients and cross‑functional teams across multiple formats.

Leadership & People Development:

  • Ability to lead, coach, and mentor others while contributing to a collaborative, high‑performing team environment.

It’s time for your next chapter: We look forward to receiving your application.

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Contact Details:

NextPharma Technologies Holding Ltd Recruitment Team

We think you need these skills to ace Scientist Formulation Development

Pharmaceutical Sciences
Formulation Development
cGMP
FDA Regulations
MHRA Regulations
Lipid-based Formulations
Hot Melt Extrusion