Location:
Livingston, GB, EH53 0TH
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Job Function: Development
Anticipated Start Date: 14 Aug 26
Job Type: Full-Time
Are you looking for...
an exciting professional challenge?
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 Development Analyst:
To conduct analysis, technical stability studies, and the development, validation and transfer of analytical methods. The role will be responsible for providing technical expertise at both a theoretical and practical level. The ideal candidate will therefore have a pharmaceutical analysis background and have gained experience within a cGMP, FDA and MHRA regulated environment. The successful candidate will thrive in a collaborative, fast-paced environment and play an active role in analytical testing of complex formulations from development through to clinical manufacture.
Key responsibilities and accountabilities:
Actively participate in, and take ownership of, analytical activities to determine the fitness for purpose of finished products ensuring compliance with regulatory and quality standards
Conduct analysis to support formulation development
Perform method development, validation and transfer of analytical methods for liquid filled hard capsules.
Conduct technical stability analysis
Conduct analysis to support product progression through clinical phases
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
Technically competent in analytical activities (e.g., method development and validation, HPLC, GC, Karl Fischer and Dissolution) under current cGMP and ICH Q2.
Take responsibility for the preparation of high-quality client documentation, including development and validation protocols and reports
Checking of analytical data
Provide expert technical support, troubleshooting, root cause analysis, and process optimisation initiatives, ensuring analytical methods are fit for purpose
Contribute to a high-performing team environment by mentoring and developing less experienced colleagues, fostering engagement, knowledge sharing, and continuous improvement
Person Profile: Development Analyst
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:
Relevant qualification, HNC/HND/Science Degree or Equivalent in Pharmaceutical Sciences, Chemistry, or a related discipline
An understanding of drug development and manufacturing processes
Demonstrated technical competence in the technical and practical skills involved in analytical activities to prescribed quality standards
Must be skilled in analytical techniques e.g., HPLC, Dissolution, Gas Chromatography, and Karl Fischer techniques
Experience of the technical and practical skills involved in stability studies, method development, transfer and validation
Able to communicate well with other colleagues, both laboratory and non-laboratory based
A self-motivated and proactive approach, with the ability to work independently while taking ownership of deliverables
Good understanding of working within a cGMP/GLP environment.
Desired:
Experience of working within a fast paced pharmaceutical or biotechnology industry
Minimum 3 years previous relevant experience in similar environment
Ability to work to key regulatory and compliance requirements
Experience of Chromeleon software
Experience of chemical analysis within a pharmaceutical environment (with drug products for preclinical and clinical trials).
Experience of data reporting and data checking to GMP standards
Able to work with minimal supervision and provide guidance to junior analysts
Understand and demonstrate a pragmatic approach to problem solving within GMP constraints
Able to communicate well via written media with specific emphasis on report writing
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
Please note – only applicants with a permanent Right to Work in the UK will be considered
Remuneration Package:
Basic Salary: £DOE
Private Medical Insurance
Health Cash Plan
Contributory pension scheme
Life Insurance
NextPharma is an equal opportunities employer and positively encourages applications from suitably qualified and eligible candidates regardless of sex, race, disability, age, sexual orientation, marriage or civil partnership, pregnancy or maternity, religion or belief.
It's time for your next chapter:
We look forward to receiving your application.
