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Eurofins

Analytical Chemist - Oligonucleotide Testing

1h

Eurofins

Lancaster, US · Full-time · $65,000 – $95,000

About this role

Eurofins Scientific is an international life sciences company providing a unique range of analytical testing services to make life and our environment safer, healthier and more sustainable. The Oligonucleotide Scientist is responsible for developing, optimizing, validating, and executing analytical methods to support oligonucleotide API, drug substance, and drug product testing.

This role supports pharmaceutical clients throughout various stages of the drug pipeline but does not include synthesis or manufacturing of oligonucleotides. The scientist focuses primarily on HPLC/UHPLC and mass spectrometry (e.g., LC-MS, LC-MS/MS) for identity, purity/impurity profiling, quantitation, and stability-indicating assessments.

The scientist will author methods, protocols and reports, ensure data integrity and compliance within GxP environments, and provide technical leadership for routine testing and investigations. Additional responsibilities include performing a large variety of analytical tasks for the validation of analytical methods used in the testing of drug products and raw materials.

This role offers the opportunity to work with a global leader in pharmaceutical and cosmetic product testing, with a rapidly developing presence in specialized molecular clinical diagnostic testing. The Eurofins network of 900 laboratories in over 54 countries provides a decentralized and entrepreneurial environment for professional growth.

Requirements

  • At least a BS or MS degree in Analytical Chemistry or related scientific discipline
  • Excellent communication (oral and written) and attention to detail
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
  • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
  • Applicants MUST have authorization to work in the U.S. indefinitely without restriction or sponsorship

Responsibilities

  • Develop, optimize, validate, and execute analytical methods to support oligonucleotide API, drug substance, and drug product testing
  • Perform a large variety of analytical tasks for the validation of analytical methods used in the testing of drug products and raw materials by means of various procedures including HPLC, GC, UV/Vis, and dissolution
  • Author methods, protocols and reports, ensuring data integrity and compliance within GxP environments
  • Conduct analytical investigations and troubleshoot instrumentation, communicating with vendors when required
  • Train and mentor junior staff in laboratory procedures
  • Manage and discuss projects with clients
  • Apply GMP in all areas of responsibility, as appropriate

Benefits

  • Work with a global leader in pharmaceutical and cosmetic product testing
  • Access to a decentralized and entrepreneurial network of 900 laboratories in over 54 countries
  • Opportunity to support pharmaceutical clients throughout various stages of the drug pipeline
  • Role focused on analytical method development and validation without synthesis/manufacturing responsibilities