More jobs:
Analytical Scientist
Job in
South San Francisco, San Mateo County, California, 94083, USA
Listed on 2026-02-14
Listing for:
Astrix
Full Time
position Listed on 2026-02-14
Job specializations:
-
Research/Development
Clinical Research, Research Scientist -
Science
Clinical Research, Research Scientist
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.
- 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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