Specialist Analytical Development

NextPharma Technologies Holding Ltd; Livingston; On-site; GBP 50,000 - 75,000; Full time

Job summary

NextPharma Technologies Holding Ltd is seeking a Development Analyst to conduct analytical testing, stability studies, and method transfer from development through clinical manufacture. The role requires a pharmaceutical analysis background, experience in a cGMP, FDA and MHRA regulated environment, and the ability to work in a fast-paced, collaborative setting.

The successful candidate will mentor junior staff, contribute to data interpretation, and prepare high-quality client documentation and

Qualifications

• Qualified in Pharmaceutical Sciences, Chemistry, or related discipline and relevant industry background.
• Experience with analytical method development, validation and transfer to GMP standards.
• Proficient in analytical techniques including HPLC, Dissolution, GC and Karl Fischer.
• Experience with stability studies and data reporting to GMP/ICH standards.
• Ability to communicate clearly with colleagues and clients and deliver reports.

Responsibilities

• Actively participate in analytical activities to determine fitness for purpose and ensure regulatory compliance.
• Conduct analysis to support formulation development.
• Perform method development, validation and transfer of analytical methods for liquid filled products.
• Lead planning, execution and reporting of experimental work to high scientific standards.
• Provide expert technical support, troubleshooting, and root cause analysis to improve processes.

Skills

Analytical methods

HPLC

Dissolution

Gas Chromatography

Karl Fischer

Method development

Data interpretation

Education

HNC/HND/Science Degree or Equivalent in Pharmaceutical Sciences, Chemistry, or a related discipline

Tools

Chromeleon

Job description

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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.
• 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

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.

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We look forward to receiving your application.