Drug Substance Development Scientist

Eurofins; Macclesfield; On-site; GBP 35,000 - 54,000; Full time

Benefits offered by this job

Reward and recognition scheme

Health cash plan

Life Assurance from day one

Company Pension Plan after 3 months

Employee Assistance Programme

Volunteering opportunities

Free on-site car parking

Perkbox access

Job summary

Eurofins is seeking an Analytical Chemical Development Scientist to provide analytical support for drug substance manufacturing and method development, performing analyses, method development, and validation activities. You’ll contribute to documentation and data interpretation within a collaborative team.

You will work in a regulated environment, applying GMP principles, and you will communicate findings to stakeholders while driving quality, accuracy and timely delivery of results.

Qualifications

• Degree in Chemistry/Analytical Chemistry with strong chemistry fundamentals.
• Experience in pharmaceutical analysis in a development lab.
• Exposure to modern analytical techniques (HPLC/GC) with method development.
• Familiarity with GMP in a regulated environment.
• Strong documentation and data interpretation skills.

Responsibilities

• Provide analytical support for drug substance manufacturing and method development projects.
• Perform project analysis, method development, forced degradation studies, and validation work.
• Contribute to authoring and review of Analytical Testing Plans and validation protocols.
• Work independently and within a multidisciplinary team to deliver analytical solutions.
• Apply strong technical expertise and problem-solving to complex projects.
• Communicate findings with stakeholders and support continuous improvement.

Skills

Chemistry knowledge

Analytical thinking

Troubleshooting

Communication skills

Education

Degree in Chemistry or Analytical Chemistry

Tools

HPLC

GC

NMR

LC-MS

IC

ICP-MS

Job description

Eurofins is seeking an Analytical Chemical Development Scientist to provide analytical support for drug substance manufacturing and method development, performing analyses, method development, and validation activities. You’ll contribute to documentation and data interpretation within a collaborative team.

You will work in a regulated environment, applying GMP principles, and you will communicate findings to stakeholders while driving quality, accuracy and timely delivery of results.