Role Overview
Join a supportive, innovative team at a Great Place to Work certified organization, recognized for its exceptional culture and industry-best employee retention rate. The company is a clinical research organization (CRO) that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.
What You Will Do
Lead and support computer system/software testing activities, create and manage test documents, ensure compliance with regulatory guidelines, collaborate with IT, QA, and Functional Leads, and maintain a strong understanding of SDLC and STLC.
Why It Might Be a Fit
The role requires excellent documentation and communication skills, detail-oriented and process-driven, with the ability to multitask, attention to detail, and organizational skills. Prior experience in clinical research or pharmaceutical domain is a must.
Requirements
- Graduate degree in scientific, medical, clinical discipline or related field, or related experience
- 5-8 years of experience in Software Quality/Testing
- Prior experience in clinical research or pharmaceutical domain is a must
- Understanding of GAMP 5, GxP, 21 CFR Part 11 and other applicable regulations
- Excellent documentation and communication skills
- Detail-oriented, process-driven, and proactive in identifying test scenarios, risks or gaps
- Excellent ability to multitask, attention to detail, and organizational skills
- Excellent ability to understand technology/software and design testing approach
Benefits
- Dental insurance
- Vision insurance
- Health insurance
- Paid time off
- Retirement plan
- Learning budget
- Parental leave
- Wellness program
- Visa/relocation support
- Remote flexibility
To apply for this job please visit mmsholdingsinc.applytojob.com.

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