Analytical Chemistry Scientist II

JOB TITLE: Analytical Chemistry Scientist II LOCATION: San Diego, CA - Onsite SCHEDULE: 8:00 AM - 5:00 PM DURATION: 12-month contract PAY: 40-45 USD per hour Job Responsibilities:In this role, you will support analytical method development, validation, and transfer within a fast-paced biopharmaceutical environment focused on oligonucleotide synthesis and testing. Key responsibilities include: Developing, optimizing, validating, and transferring analytical methods for oligonucleotides, raw materials, and reagent consumables Designing, planning, and executing laboratory experiments with minimal supervision Managing multiple assignments and delivering high-quality results within project timelines Performing data analysis, interpreting results, and troubleshooting analytical issues Preparing study protocols, technical reports, and assay work instructions with high attention to detail Ensuring compliance with GMP, Good Documentation Practices (GDP), and internal quality standards Supporting cross-functional collaboration and continuous improvement initiatives Performing additional duties as assigned by management Essential Duties and Job Functions:Execute and support analytical method development, qualification, validation, and transfer activities Perform hands-on laboratory work using chromatographic and spectroscopic techniques Conduct oligonucleotide characterization and release testing Ensure accurate documentation and adherence to regulated laboratory practices Investigate and resolve unexpected analytical results using scientific problem-solving approaches Collaborate with cross-functional teams to support method lifecycle activities Contribute to assay development, optimization, and standardization efforts Maintain compliance with FDA cGMP, ICH guidelines, USP requirements, and internal quality systems Support continuous improvement initiatives within analytical development workflows Knowledge & Skills:Strong hands-on laboratory skills with excellent organization and documentation practices Proficiency in analytical techniques including HPLC, LC-MS, UV-Vis, FTIR, Karl Fischer, and NMR Experience with oligonucleotide analysis and characterization Strong understanding of method development, validation principles, and regulatory expectations (FDA, ICH, USP) Excellent problem-solving, analytical thinking, and troubleshooting abilities Ability to manage multiple priorities in a fast-paced, deadline-driven environment Strong communication skills (verbal and written) and ability to collaborate across teams Familiarity with GMP environments and quality systems High attention to detail and commitment to data integrity Ability to work independently while contributing effectively in a team setting Education & Experience:Bachelor's, Master's, or Ph.D. in Analytical Chemistry, Chemistry, Biochemistry, Molecular Biology, or related scientific field Minimum 2 years of hands-on experience in analytical method development, validation, qualification, and transfer Direct experience with oligonucleotide analytical testing strongly preferred Experience working in GMP-regulated or pharmaceutical/biotech environments preferred Strong academic or industry background in chromatographic and spectroscopic methods required ...