Analytical Scientist

Astrix; South San Francisco (CA); On-site; USD 61,992 - 68,880; Full time

Job summary

A leading pharmaceutical company in South San Francisco is seeking an experienced Analytical Scientist to join their Pharmaceutical Sciences team. The role involves hands-on work in HPLC method development and stability testing within a collaborative and fast-paced environment. Ideal candidates have substantial experience in pharmaceutical analysis, knowledge of GLP/GMP standards, and a commitment to laboratory safety. This position offers competitive pay to foster innovation and growth in cancer therapies.

Qualifications

• 3+ years of relevant pharmaceutical or biotech experience for B.S., or 1+ year for M.S.
• Experience with analytical techniques including HPLC, LC-MS, GC.
• Knowledge of GLP/GMP standards and FDA guidance.

Responsibilities

• Perform HPLC method development and troubleshooting.
• Conduct stability testing and analytical testing on tablets.
• Prepare samples and maintain accurate lab documentation.

Skills

HPLC method development

Stability testing

Dissolution testing

Chromatography

Spectroscopy

Problem-solving skills

Attention to detail

Education

B.S. in Chemistry

M.S. in Chemistry

Tools

Empower

ChemStation

Excel

Job description

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, ChemStation, 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.