Lead Analytical Development Scientist

LabRulez; Macclesfield; Hybrid; GBP 40,000 - 60,000; Full time

Benefits offered by this job

Holiday entitlement increases with 서비스

Health Cash Plan

Life Assurance

Company Pension Plan

Employee Assistance Programme

Perkbox

Free on-site car parking

Volunteering opportunities

Job summary

Eurofins Scientific is seeking an Analytical Chemical Development Scientist to lead analytical activities for drug substances and method development. You will oversee project analyses, method development, forced degradation, and validation work in a fast-paced, quality-driven environment.

The role requires a strong background in HPLC/GC, NMR, LC-MS, and ICP-MS, with GMP awareness and excellent documentation and communication skills to support customers and regulatory requirements.

Qualifications

• Degree in Chemistry or Analytical Chemistry with strong organic chemistry and analytical science knowledge.
• Experience in pharmaceutical analysis within a development laboratory is advantageous.
• Experience with modern analytical techniques (HPLC/GC) and development/validation experience is desirable.

Responsibilities

• Provide analytical support for drug substance manufacturing and method development projects.
• Conduct project analysis, method development, forced degradation, and validation work.
• Contribute to authoring and reviewing analytical documentation such as testing plans and validation protocols.
• Work independently and in multidisciplinary teams to deliver analytical solutions.
• Apply scientific expertise to investigate challenges and develop robust approaches.
• Communicate findings effectively with internal and external stakeholders and support continuous improvement.

Skills

HPLC

GC

NMR

LC-MS

ICP-MS

IC

GMP knowledge

Data interpretation

Communication

Documentation

Education

Degree in Chemistry or Analytical Chemistry

Tools

Microsoft Office

LIMS

Job description

Eurofins Scientific is seeking an Analytical Chemical Development Scientist to lead analytical activities for drug substances and method development. You will oversee project analyses, method development, forced degradation, and validation work in a fast-paced, quality-driven environment.

The role requires a strong background in HPLC/GC, NMR, LC-MS, and ICP-MS, with GMP awareness and excellent documentation and communication skills to support customers and regulatory requirements.