| Job Description | Description
Theranos is actively building a world-class team. Ideal candidates are currently employed or have been employed in similar types of positions and want to be part of a paradigm-shifting company doing innovative work. Candidates must be hard-working with an unfaltering determination to excel in an intense start-up environment and a desire to gain tremendous personal and career growth.
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 Validation Supervisor.
Requirements:
Requires Master's degree or equivalent in Biomedical Science, Biological Science, or related; and 3+ years of experience in life science research
Experience in validation of assays for biomolecules.
Experience in FDA and ICH validation guidelines.
Must also have experience in standard analytical methods, reagent preparation and tools
Experience in working with biological specimens
Experience in CLIA lab or CLS license is preferred
Proficient in MS Word, Excel, use of statistical analysis software
Strong interpersonal skills to enable interface with fellow Technicians, and Quality Supervisor/Manager, and personnel from R&D & 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 |
| | Company | | Theranos | Job Code | | State or Province | | California | | |
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