Scientist I - III
Rani Therapeutics
June 30, 2026
On-site
Fremont, CA
$80,000 - $179,000 USD yearly
Clinical Research and Development
Job Duties:
- Conduct analysis or experiments by following procedures independently.
- Conduct lot release and stability testing in compliance with GMP/GLP, safety and regulatory requirements to support all development stages.
- Develop and execute experimental plans of limited scope (e.g., method development, characterization studies, instrument qualification) with minimum supervision.
- Assist in developing and validating moderately complex analytical methods to test raw materials, intermediates and final products, or quantify biomarkers in biological matrices.
- Help improve existing complex methods with supervision.
- Analyze and interpret complex data following procedures.
- Learn and apply basic GMP/GLP principles.
- Review test records according to procedures.
- Maintain laboratory safety and alertness for the safety of coworkers and visitors.
Education and/or Job Experience:
- BS with a minimum of 5 years, or MS with a minimum of 3 years of relevant pharmaceutical or biotechnology development experience.
Preferred Qualifications:
- Working knowledge of biophysical techniques and analytical characterization of peptides and proteins.
- Experience supporting formulation and process development.
- Aseptic processing experience.
- Experience authoring/revising SOPs, work instructions, test methods, batch records, validation protocols, development reports, and validation reports.
- Experience in GLP/GMP regulated environments.
- Excellent oral and written communication skills.
- Ability to work as part of a multidisciplinary team.
- Conduct analysis or experiments by following procedures independently.
- Conduct lot release and stability testing in compliance with GMP/GLP, safety and regulatory requirements to support all development stages.
- Develop and execute experimental plans of limited scope (e.g., method development, characterization studies, instrument qualification) with minimum supervision.
- Assist in developing and validating moderately complex analytical methods to test raw materials, intermediates and final products, or quantify biomarkers in biological matrices.
- Help improve existing complex methods with supervision.
- Analyze and interpret complex data following procedures.
- Learn and apply basic GMP/GLP principles.
- Review test records according to procedures.
- Maintain laboratory safety and alertness for the safety of coworkers and visitors.
Education and/or Job Experience:
- BS with a minimum of 5 years, or MS with a minimum of 3 years of relevant pharmaceutical or biotechnology development experience.
Preferred Qualifications:
- Working knowledge of biophysical techniques and analytical characterization of peptides and proteins.
- Experience supporting formulation and process development.
- Aseptic processing experience.
- Experience authoring/revising SOPs, work instructions, test methods, batch records, validation protocols, development reports, and validation reports.
- Experience in GLP/GMP regulated environments.
- Excellent oral and written communication skills.
- Ability to work as part of a multidisciplinary team.