Analytical Chemistry Scientist

Target PR Range:
36.25-45/hr DOE

JOB DESCRIPTION

As an
Analytical Chemistry Scientist II
within Analytical Method Development and Transfer Group, you will play a key role in developing, validating, and, transferring analytical methods that support oligonucleotides synthesis and release testing, and raw material qualification. You will work in a fast?paced, collaborative environment, partnering with cross?functional teams to ensure high?quality analytical support across multiple programs. This role requires deep technical expertise in chromatographic and spectroscopic techniques, strong problem?solving

skills, and hands?on laboratory experience.

• · Develop, optimize, validate and transfer analytical methods for oligonucleotides, raw materials, and reagent consumables.
• · Design, plan and execute various laboratory experiments with minimal supervision.
• · Prioritize multiple assignments and deliver high-quality results within established project timelines.
• · Analyze data analysis, interpret results, and troubleshoot unexpected analytical outcomes.
• · Prepare study protocols and reports, and assay work instructions with attention to details.
• · Ensure compliance with GMP, Good Documentation Practice (GDP), and quality standards.
• · Contribute to a positive, collaborative, and continuous-improvement-focused team culture.
• · Perform additional duties as assigned by manager.

• · BS/MS/Ph.D in Analytical Chemistry, Chemistry, Biochemistry, Molecular Biology, or a related scientific discipline.
• · Minimum 3 to 4
  years of hands-on experience
  in analytical method development, qualification, validation and transfer.
• · Proficient with analytical techniques including
  HPLC, LC-MS, UV-Vis, FTIR, Karl Fischer, and NMR.
• · Experience in analytical characterization and testing of
  oligonucleotides
  .
• · Demonstrated ability to perform and collaborative effectively across multidisciplinary teams.
• · Strong laboratory execution skills, including organization, documentation, and adherence to quality systems.
• · Excellent verbal/written communication skills.
• · Working knowledge of method validation principles and for regulatory expectations (FDA cGMP; ICH, USP).