Validation Chemist
Theranos is actively
building a world-class team. Most likely candidates are currently
employed in similar types of positions but want to be part of a
paradigm-shifting company doing innovative work and gain tremendous personal
and career growth. Candidates must be hard working with unfaltering
determination to excel in an intense start-up environment.
Responsibilities
- To analyze and validate assay systems to assure and document that products meet specifications.
- To perform quality calibrations, internal audits, and project assignments in a timely, safe, professional manner, reporting results, issues, or roadblocks, to the Validation Supervisor.
Requirements
- Requires master's degree or foreign degree equivalent in biomedical science, biological science, or related; and 3+ years of experience in life science companies.
- Experience in assay development.
- Must also have experience in standard analytical methods, reagent preparation, and tools.
- Experience in working with biological specimens like blood, serum.
- Proficient in MS Word, Excel, use of statistical analysis software.
- Strong interpersonal skills to enable interface with fellow Technicians, Quality Supervisor/​Manager, and personnel from R&D and Production.
- Organizational skills to maintain orderly documentation needed and to Multi-task.
- Author and coordinate the execution of qualification and validation protocols as defined by the validation program in support of multiple projects.
- Great attention to detail.
Contact us at careers@theranos.com.
Notice to recruiting agencies:
Theranos, Inc. ('Theranos') does not accept unsolicited resumes from recruitment agencies, search firms, headhunters, or staffing agencies. Please do not forward resumes to our careers alias or to any employee, contractor or consultant of Theranos. Any unsolicited resume submitted will be considered property of Theranos, and we will not be obligated to pay any fee associated with such resume.