Senior Quality Assurance Specialist/ Quality Assurance Specialist

Passionate about precision medicine and advancing the healthcare industry?

Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.

• Responsibilities:
• Compilation and approval of the Device History Record.
• Complete incoming material acceptance activities.
• Read, understand, and update SOPs within the document control system, including creation/revision/review of internal SOPs and other quality documentation.
• File quality documentation in a systematic organized manner.
• Maintain documentation in order to satisfy CLIA/CAP/NYS-DOH/FDA requirements.
• Provide metrics to identify trends and conduct root cause analysis, and develop corrective actions to prevent the recurrence of quality issues.
• Report significant deviations and system deficiencies to management, as appropriate.
• Interact with management and testing personnel to coordinate Quality tasks.
• Pull records and reports as requested during internal and external audits.
• Help facilitate and implement corrective and preventative actions
• Aid in tracking and maintenance of quality records, including batch records, checklists, competency assessments, quality and equipment binders, and continuing education documentation.
• Complete and maintain onboarding, offboarding, and transfer duties within electronic quality management systems.
• Maintain training matrix and training document master list.
• Assist in document control workflow, as needed.

• Qualifications:
• High school diploma required, Bachelors Degree in Science or Engineering preferred.
• 2-4 years of experience with clerical/documentation handling.
• Highly organized and systematic, with superb attention to detail.
• Ability to complete repetitive tasks with a high degree of precision and accuracy.
• Proven ability to learn new skills quickly and adapt to new processes smoothly.
• Excellent time management and communication skills.
• Self-driven and works well in a fast-moving, cross-functional team environment with minimal direction.
• Ability to create processes and workflows, as well as define and create solutions to challenges.
• Intermediate computer skills and software applications, including experience with Microsoft Office tools and/or Google Suite applications.
• This position is onsite.
• Previous experience in a clinical lab regulated by CAP/CLIA/NYS/FDA highly desirable.CHI: $55,000-$70,000
• The expected salary range may vary for other locations. Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.

We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.