Impactful Work Awaits

Signant Health, a leader in evidence generation, empowers clinical trial programs through innovative technology. Join us in a dynamic, high-growth environment.

Your Role as Quality Specialist

Responsible for quality review of documentation for computerized system validation related to clinical studies.

Team Collaboration

We are looking for individuals who enjoy making a difference, with a focus on open communication and collaboration.

Main Responsibilities

• Provide expertise on quality processes.
• Support CAPA and quality audits.
• Identify non-conformances and implement improvements.
• Assist in maintaining compliance with regulations.
• Raise quality challenges and support resolution.

Decision-Making and Influence

• Interact effectively with cross-functional teams.
• Foster open communication and cooperation within departments.

Qualifications

• Associate degree or equivalent education required.
• 3+ years of GxP experience with knowledge of compliance in software development.
• Strong analytical and time-management skills.
• Willingness to travel and work non-standard hours.
• Bachelor's degree preferred.

Location

Santiago, RM, Chile

Join Us

Apply now and become part of our exciting journey at Signant Health, where we celebrate diversity and equal opportunity for all.