Quality Control Analyst (Compliance & Quality)
Required skills
- Quality Control Analyst
- Compliance
- Quality
- GxP
- 21 CFR Part 312
- 21 CFR Part 11
- Annex 11
- ICH E6
- SDLC
- validation deliverables
Nice to have
- clinical trial industry
- Suvoda software products
- Suvoda procedures
Role summary
Suvoda, a clinical trial technology company, seeks a Quality Control Analyst with 1-3+ years of experience to ensure compliance and quality in software development and delivery. Responsibilities include identifying and reporting issues, releasing products, reviewing SDLC and validation deliverables, performing in-process verifications, and supporting IT validation projects. The role also involves onboarding third-party vendors and participating in process improvement initiatives. Preferred knowledge of GxP regulations (21 CFR Part 312, Part 11, Annex 11, ICH E6). Requires strong attention to detail, time management, and a proactive attitude.
Suvoda is a global clinical trial technology company shaping digital experiences that enable clinical trial sponsor and site professionals to take full command over the inherent logistical complexity behind mission-critical and time-sensitive patient interactions in life-sustaining studies for therapeutic areas such as oncology, central nervous system, and rare disease.
Supporting clinical trials means supporting unique experiments that are inherently complex, high-stakes, and dynamic. It is imperative that Suvoda staff working with clients, end-users, or the systems that client and end-users interact with understand the clinical trial industry, regulations, Suvoda’s software products and processes, and especially the specificities of the unique trial in question before taking any actions they may alter the data of the system in question.
Responsibilities:
Requirements:
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