Quality & Compliance Analyst
RemoteIndia
IndiaRemoteFull TimeTECHMedium
Full TimeMediumTECH
Job Summary
Manage inbound security and quality questionnaires across SOC 2, ISO 9001, ISO 27001, and CMMC frameworks, utilizing our answer library to ensure rapid, accurate responses. Own day-to-day QMS operations, including training assignments, change order records, and supplier data, maintaining accuracy for real-time reporting in Jira and Confluence. Serve as a trusted reviewer of control statements and SOPs, catching evidence drift before audits while leading the team through end-to-end certification cycles.
Required Qualifications
- 2–5 years in GRC, compliance operations, quality assurance, or audit support, in a role where you did the hands-on work yourself
- Direct experience responding to security or quality questionnaires at volume, and comfort owning the shared tooling and answer library behind those responses
- Hands-on involvement in at least one audit or certification cycle end to end, SOC 2, ISO 9001, ISO 27001, CMMC, or a comparable framework, including evidence collection and findings follow-up
- Experience as the day-to-day administrator or power user of a compliance system of record (eQMS, GRC platform, or equivalent), with real accountability for data accuracy
- Strong technical writing and editing
- Fluency in Jira and Confluence, and the discipline to keep them current without being reminded
- Real fluency with agentic AI tooling and frameworks, you've built custom skills, agents, or prompt-driven workflows to take repetitive work off your own plate, and you know where model output has to be human-verified
- Meticulous attention to detail and calendar discipline
- Sound judgment about the limits of your own knowledge, you know when to answer, when to pull in an SME, and when to escalate. You never invent an answer to a customer-facing security question
- A collaborative, low-ego approach to working across Security, Engineering, Legal, People, and Sales
Desired Qualifications
- Nice to have: experience in a regulated life-sciences, medical device, or pharmaceutical environment, GxP, 21 CFR Part 11, computer system validation, or supplier qualification
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