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Analytical Scientist

Job in South San Francisco, San Mateo County, California, 94083, USA
Listing for: Astrix
Full Time position
Listed on 2026-02-14
Job specializations:
  • Research/Development
    Clinical Research, Research Scientist
  • Science
    Clinical Research, Research Scientist
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below

Pay Rate Low: 45 | Pay Rate High: 50

Our client is seeking a highly motivated Anlaytical Scientist to join a growing Pharmaceutical Sciences team focused on advancing innovative cancer therapies. This is an excellent opportunity for a hands‑on scientist who enjoys contributing across multiple projects in a collaborative, fast‑paced environment.

What You’ll Do
  • Perform HPLC method development and validation, including troubleshooting and optimization, to support drug development activities.
  • Conduct stability testing in accordance with ICH guidelines, including sample analysis, data interpretation, and documentation.
  • Execute analytical testing on solid oral dosage forms (tablets) using techniques such as HPLC, LC-MS, GC, UV‑Vis, Karl Fischer, and dissolution testing.
  • Perform dissolution testing for tablets and other dosage forms to support formulation development and stability studies.
  • Operate laboratory software to control instruments, collect and analyze data, and generate clear, well‑documented reports.
  • Prepare samples, reagents, standards, and test solutions in strict accordance with SOPs and compendial methods.
  • Maintain accurate, compliant laboratory documentation to ensure data integrity, traceability, and regulatory readiness.
  • Summarize and present analytical results to management and at internal or external meetings.
  • Collaborate closely with cross‑functional partners in Process Chemistry and Formulation Development.
What We’re Looking For
  • B.S. in Chemistry with 3+ years of relevant pharmaceutical or biotech experience, or M.S. in Chemistry with 1+ year of industry experience.
  • Strong hands‑on experience with HPLC method development and validation, stability testing, dissolution testing, and analysis of tablet dosage forms.
  • Experience with chromatography, spectroscopy, titration methods, and other compendial analytical techniques.
  • Proficiency with laboratory and data analysis software (e.g., Empower, Chem Station, Excel).
  • Solid understanding of GLP/GMP and industry standards, including ICH, USP, and FDA guidance.
  • Strong problem‑solving skills with the ability to take ownership of analytical work and contribute to experimental design.
  • Excellent attention to detail, organization, and commitment to laboratory safety.
  • Ability to work independently while thriving in a collaborative, multidisciplinary team.
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