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Eurofins Verified 40h ago

Oligonucleotide Method Development & Validation

Lancaster, PA, United States On-site

Salary not listed
PaySalary not listed
TypeFull-time
Work settingOn-site
Verified listing

JobFig found this opening at its original source and checks that it remains available.

About the role

The Oligonucleotide Scientist is responsible for developing, optimizing, validating, and executing analytical methods to support oligonucleotide API, drug substance, and drug product testing.  The role supports pharmaceutical clients throughout various stages of the drug pipeline but does not support or include synthesis/manufacturing of oligonucleotides. The role 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 and mentoring of junior staff. Additional tasks/skills will include: Performing 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. Reading, understanding, and interpreting diverse analytical procedures. Conducting analytical investigations. Troubleshoot instrumentation and communicate with vendors when required.

What you'll bring

  • At least a BS or MS degree in Analytical Chemistry or related scientific discipline • BS and 4+ years, MS and 2+ years, or PhD and 1+ year of relevant industry experience
  • Experience performing analytical testing with oligonucleotides in a GMP-regulated environment
  • Technical Expertise: Strong theoretical and practical knowledge of chromatography (HPLC, UHPLC, IEX, SEC) and mass spectrometry, including method development, validation, and routine testing
  • Regulatory Knowledge: Familiarity with ICH guidelines and GxP regulatory standards
  • Background should be primarily in analytical testing or analytical method development
  • candidates with primarily synthesis or process chemistry experience without analytical/QC responsibilities will not be considered

Benefits

401(k)Disability InsuranceMedical InsurancePaid Time Off