E

Eurofins

Global lab testing and analytics network

Analytical Chemical Development Scientist

Bioprocess & BiomanufacturingPosted on Nov 9
Full-timeMacclesfield, UKNo salary listed

About the Job

Requirements

  • Hold a degree in Chemistry or Analytical Chemistry and have strong fundamental knowledge of chemistry, particularly organic chemistry and analytical science.
  • Have experience in pharmaceutical analysis within a development laboratory.
  • Have experience with modern analytical techniques, including high-performance liquid chromatography (HPLC) and gas chromatography (GC).
  • Have knowledge of raw materials, intermediates, drug substance analysis, and peptide chemistry, alongside a strong understanding of good manufacturing practice (GMP) requirements and best practices within a regulated environment.
  • Have troubleshooting, problem-solving, and technical skills; be able to learn new processes quickly, use electronic systems and Microsoft Office applications effectively, and adapt to changing priorities.
  • Have communication, organisational, and documentation skills, and be able to build relationships with colleagues and clients and work independently and collaboratively.

Responsibilities

  • Provide analytical support for drug substance manufacturing and method development projects, delivering analytical testing in line with client and regulatory requirements.
  • Perform project analysis, method development activities, forced degradation studies, proof-of-concept validation work, and data interpretation to support scientific objectives.
  • Contribute to authoring and reviewing analytical documentation, including Analytical Testing Plans, method protocols, and validation protocols, according to skills and experience.
  • Work independently and collaboratively within a multidisciplinary team to deliver accurate, innovative, and timely analytical solutions.
  • Investigate challenges, think logically, and develop scientific approaches to complex projects.
  • Communicate scientific findings and ideas to internal and external stakeholders and contribute to continuous improvement, knowledge sharing, and professional development.

Desired Qualifications

  • Knowledge of pharmaceutical development, quality control environments, and the drug development process.
  • Experience in method development and validation.
  • Knowledge of nuclear magnetic resonance (NMR), liquid chromatography-mass spectrometry (LC-MS), ion chromatography (IC), and inductively coupled plasma mass spectrometry (ICP-MS).

About the Company

Eurofins

Global lab testing and analytics network

Eurofins provides global laboratory testing and analytical services to verify the safety, authenticity, and quality of products across food, water, medicine, and the environment. It operates a network of more than 900 laboratories in over 60 countries, offering access to more than 200,000 analytical methods. Its product work involves running specialized tests—using chemistry, biology, and other scientific techniques—to confirm origin, composition, and compliance of samples, such as detecting wine fraud or contaminant presence. The company differentiates itself through its massive, distributed lab network and broad portfolio, enabling standardized testing at scale and fast turnaround across many industries, rather than relying on a single specialty or location. Its goal is to protect public health and safety by delivering accurate, comprehensive testing data and helping clients meet regulatory and quality requirements.

Company size
10,001+
Company stage
IPO
Headquarters
Luxembourg
Founded
1987

Recently Posted Jobs

Explore more opportunities at Eurofins

See more jobs