Scientific Associate Iii, Analytical Sciences

Pharmaron; Liverpool; On-site; GBP 36,000 - 54,000; Full time

Job summary

Pharmaron in Liverpool is seeking a Scientific Associate III to join the Biologics Analytical Sciences team. This hands-on laboratory role supports development, optimisation, phase-appropriate validation, transfer and application of analytical methods for biological products, including in-process testing and cGMP release testing.

You will collaborate with project leads and multidisciplinary teams, contribute to effective documentation, ensure compliance with GMP, EHS, and quality standards, and

Qualifications

• A-levels or equivalent in a science-related subject.
• Relevant laboratory experience in a pharmaceutical, biopharmaceutical, biotechnology or similar scientific environment.
• Strong organisational skills, attention to detail and the ability to meet project timelines.
• Effective communication, teamwork and problem-solving skills.
• A safety-focused, flexible approach and commitment to quality, regulatory and EHS standards.
• Motivation to learn and develop within analytical sciences.

Responsibilities

• Perform analytical testing to support the development and characterisation of biological products.
• Support analytical method development, optimisation, validation, transfer and application.
• Complete GMP and non-GMP testing and documentation accurately and within project timelines.
• Support project leads in delivering internal and client work packages.
• Prepare, review and report scientific documentation and analytical results with a right-first-time approach.
• Work in accordance with quality, regulatory, GMP and EHS requirements.
• Maintain laboratory equipment, reagents, consumables and high housekeeping standards.
• Support new equipment implementation and the training of colleagues.
• Develop expertise across analytical characterisation, immunoassays, molecular biology, cell-based methods and GMP analysis.
• Contribute to 5S, operational excellence and continuous improvement.
• Collaborate with multidisciplinary teams to meet project objectives and provide occasional out-of-hours cover when required.

Job description

Scientific Associate III, Analytical Sciences (Fixed Term Contract)

Location: Liverpool, UK

About Pharmaron

Pharmaron is a global contract research and manufacturing organisation (CRO/CDMO) helping pharmaceutical and biotechnology companies bring new therapies to life. With over 25,000 employees across 28 locations in the UK, US, China and Singapore, we support drug discovery through to manufacturing with fully integrated, high-quality services. We are proud of the impact we make. Last year, we supported 887 discovery projects, more than 1,100 CMC programmes and 1,397 clinical trials across all phases. Our teams work across small molecules, ADCs, biologics and gene therapies, supporting more than 3,300 customers globally. To learn more, visit www.pharmaron.com.

Our Liverpool site

Our Liverpool facility provides integrated biologics development and manufacturing services across Analytical and Process Sciences. The site has an established track record in biologics development, with capabilities supporting gene therapy drug substance development, viral vectors, plasmid DNA, analytical release testing and product characterisation.

The role

We are seeking a motivated and practical Scientific Associate III to join our Biologics Analytical Sciences team in Liverpool.

This is a hands‑on laboratory position supporting the development, optimisation, phase‑appropriate validation, transfer and application of analytical methods for biological products. You will contribute to in‑process development testing, non‑GMP activities and cGMP release testing while working closely with project leads and multidisciplinary scientific teams.

At Pharmaron, we offer

• Vibrant and dynamic employment: We are a highly specialised growth company operating in a critical sector of the economy. Our future is strong and exciting.
• Opportunities to develop your skills and yourself: Our continued growth provides opportunities for you to learn, broaden your technical expertise and develop your career.
• A supportive and collaborative team: You will work alongside experienced scientific colleagues in an environment where people support one another and share their knowledge.

Key roles and responsibilities

• Perform analytical testing to support the development and characterisation of biological products.
• Support analytical method development, optimisation, validation, transfer and application.
• Complete GMP and non‑GMP testing and documentation accurately and within project timelines.
• Support project leads in delivering internal and client work packages.
• Prepare, review and report scientific documentation and analytical results with a right‑first‑time approach.
• Work in accordance with quality, regulatory, GMP and EHS requirements.
• Maintain laboratory equipment, reagents, consumables and high housekeeping standards.
• Support new equipment implementation and the training of colleagues.
• Develop expertise across analytical characterisation, immunoassays, molecular biology, cell‑based methods and GMP analysis.
• Contribute to 5S, operational excellence and continuous improvement.
• Collaborate with multidisciplinary teams to meet project objectives and provide occasional out‑of‑hours cover when required.

Requirements

Essential

• A‑levels or equivalent in a science‑related subject.
• Relevant laboratory experience in a pharmaceutical, biopharmaceutical, biotechnology or similar scientific environment.
• Strong organisational skills, attention to detail and the ability to meet project timelines.
• Effective communication, teamwork and problem‑solving skills.
• A safety‑focused, flexible approach and commitment to quality, regulatory and EHS standards.
• Motivation to learn and develop within analytical sciences.

Desirable

• BSc, MSc or equivalent in a relevant life sciences discipline.
• Industrial experience in biopharmaceuticals or pharmaceuticals, ideally gene therapy.
• Experience in analytical method development, optimisation, validation, transfer or equipment qualification.
• Knowledge or practical experience in one or more of the following:
  • Immunoassays, including ELISA, potency or host cell protein testing
  • Molecular biology, including qPCR, ddPCR, sequencing or residual DNA testing
  • Product characterisation, including LC‑MS, AUC, DLS, DSC or TEM
• Experience in a GMP or regulated laboratory environment.
• Experience preparing scientific procedures, protocols and reports.
• Knowledge of statistical analysis and experimental design.

Why Pharmaron?

Collaborative Culture: Thrive in a supportive and inclusive environment where teamwork, learning and innovation are at the core of what we do.

Impactful Work: What you do here contributes directly to the development of life‑changing medicines.

Career Growth: We invest in your development offering continuous learning, technical training and opportunities to grow within a fast‑expanding global organisation.

People‑Centric Values: Our cultural values, Employees Number One and Clients Centered, guide everything we do and set us apart in the industry.