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Sr. Qa Specialist - Remote
Company | Medable, Inc |
Address | Palo Alto, CA, United States |
Employment type | FULL_TIME |
Salary | |
Category | Technology, Information and Internet |
Expires | 2023-06-15 |
Posted at | 1 year ago |
Company Description
Medable's mission is to get effective therapies to patients faster. We provide an end-to-end, cloud-based platform with a flexible suite of tools that allows patients, healthcare providers, clinical research organizations and pharmaceutical sponsors to work together as a team in clinical trials. Our solutions enable more efficient clinical research, more effective healthcare delivery, and more accurate precision and predictive medicine. Our target audiences are patients, providers, principal investigators, and innovators who work in healthcare and life sciences.
Our vision is to accelerate the path to human discovery and medical cures. We are passionate about driving innovation and empowering consumers. We are proactive, collaborative, self-motivated learners, committed, bold and tenacious. We are dedicated to making this world a healthier place.
Medable, Inc provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
U.S. employees and contractors, and International workers with travel to the U.S. must have a willingness and ability to provide proof of completed COVID-19 vaccination prior to start date. All strongly held beliefs, religious, medical, and other legally recognized exemptions regarding vaccination status will be considered.
Medable's mission is to get effective therapies to patients faster. We provide an end-to-end, cloud-based platform with a flexible suite of tools that allows patients, healthcare providers, clinical research organizations and pharmaceutical sponsors to work together as a team in clinical trials. Our solutions enable more efficient clinical research, more effective healthcare delivery, and more accurate precision and predictive medicine. Our target audiences are patients, providers, principal investigators, and innovators who work in healthcare and life sciences.
Our vision is to accelerate the path to human discovery and medical cures. We are passionate about driving innovation and empowering consumers. We are proactive, collaborative, self-motivated learners, committed, bold and tenacious. We are dedicated to making this world a healthier place.
- Document quality assurance activities, including, internal audits and CAPAs
- Other duties as assigned
- Ensure ongoing abidance by industry regulatory and quality requirements
- Support other departments with CAPA process, including, creation and follow through to completion, ensuring appropriate documentation is captured
- Ensure risk management procedures are utilized correctly
- Lead, assist, and/or mentor other Quality Assurance Specialists
- Report on results of quality activities
- Analyze non-compliance issues to identify trends and propose resolutions
- Interpret and comply with quality assurance standards
- Identify quality areas for improvement
- Approve event intake tickets (EITs)
- Gather and organize statistical quality data
- Ensure adequacy of current quality assurance standards and recommend enhancements
- Ensure company compliance with GxP requirements, company policies and procedures, ISO standards, and MDD/MDR requirements
- Carry out appropriate corrective procedures from internal and external audits
- Ability to handle sensitive information with the highest degree of integrity, discretion and confidentiality
- Analytical, problem-solving, and decision-making skills
- Comfort working across teams in a fast-paced environment
- Ability to write, speak, and interact clearly and professionally
- Experience working in an ISO environment
- Experience working in a quality capacity (pharmaceutical or medical device preferred)
- 5+ years of experience in a quality role or a combination of education and experience
- Bachelor’s degree in a related field
- Six Sigma Green or Black Belt
- ASQ Certified Auditor
Medable, Inc provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
U.S. employees and contractors, and International workers with travel to the U.S. must have a willingness and ability to provide proof of completed COVID-19 vaccination prior to start date. All strongly held beliefs, religious, medical, and other legally recognized exemptions regarding vaccination status will be considered.
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