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- Run and validate quality gates prior to release:
- 3–7+ years in data QA / annotation QA / operations quality; experience auditing labeled datasets (video…
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- PfizerVisakhapatnam, Andhra Pradesh
- Support quality systems such as Change Control, CAPA tracking, and document management.
- Fundamental knowledge of manufacturing and quality control processes (…
- TRIMED SOLUTION INDIA PVT LTDHyderabad, Telangana
- Identify gaps in service quality and implement process improvements.
- Monitor adherence to quality standards across all service and maintenance activities.
- VamstarRemote
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- Exposure to healthcare, pharmaceuticals, or medical devices industries.
- Deliver high-quality outputs within defined timelines.
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- DNVDelhi, Delhi
- Please note, benefits may depend on your contract type, please confirm with your recruiter.
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- EVERSANAPune, Maharashtra
- Work collaboratively with other cross-functional medical and scientific reviewers, medical writers, and creative teams across EVERSANA.
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- EVERSANAPune, Maharashtra
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- Talent Vision ServicesNoida, Uttar Pradesh
- Experience in Medical device Industry will be a bonus.
- Assist in maintaining and improving company’s quality system.
- Assisting in Design Dossier preparation.
- SFJ Business solutionsBahadurgarh, Haryana
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- DEV-XRemote
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- ThermaissanceDelhi, Delhi
- Health insurance
- Paid time off
- Paid sick time
- Provident Fund
- Work from home
- Competitive compensation with strong growth opportunities in a high-impact medical device innovation company..
- Generate high-quality clinical evidence.
- Sk Royal ConsultantBaddi, Himachal Pradesh
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- KonovoBengaluru, Karnataka
- Health insurance
- Exceptional attention to detail with consistently high accuracy in transcription and quality review.
- Strong command of medical terminology and the ability to…
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- pharmacuiticalsPaonta Sahib, Himachal Pradesh
- Health insurance
- Provident Fund
- * Handling BMR / BPR, SOP, STP and other quality documents.
- * Preparation and review of QA documentation.
- * Documentation control and record maintenance.
- Siemens HealthineersBengaluru, Karnataka
- 3–7 years of experience in Quality Engineering, QMS support, or Quality Operations within the medical device or regulated industry.
- NeST DigitalBengaluru, Karnataka
- At least 6-8 years of overall experience in software quality assurance, including testing medical device products.
Job Post Details
(US) QA Auditor (Sampling, Quality Gates, Release Readiness) - job post
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Job details
Job type
- Full-time
Full job description
QA Auditor (Sampling, Quality Gates, Release Readiness) - USA
JD: QA Auditor — Surgical Video Annotation (Sampling, Quality Gates, Release Readiness)
Location: USA | Type: Full-time
Reports to: Quality Lead / Program Lead
Role goal: Protect dataset quality at scale by running sampling-based audits, enforcing quality gates, and ensuring every dataset release is audit-ready and meets acceptance thresholds.
About Us
At Codvo, we are committed to building scalable, future-ready data platforms that power business impact. We believe in a culture of innovation, collaboration, and growth, where engineers can experiment, learn, and thrive. Join us to be part of a team that solves complex data challenges with creativity and cutting-edge technology.
Responsibilities
Execute sampling plans (stratified by label type, difficulty, site/surgeon/device, model confidence) for ongoing QA and release audits.
Audit annotations against guidelines + ontology; score defects using standardized rubrics (severity, type, root cause).
Run and validate quality gates prior to release:
completeness/coverage checks
schema/constraint checks (illegal combinations, temporal consistency, boundary rules)
defect density and rework thresholds
Generate rework tickets with precise instructions; track closure and verify fixes.
Partner with Annotation Lead to drive calibration actions (training refreshers, guideline clarifications, examples library).
Maintain QA dashboards: defect rate, rework %, gate pass rate, audit cycle time, top error patterns by annotator/team/label type.
Support release readiness: ensure required artifacts are complete for the Evidence Pack (QA results, sampling logs, sign-offs).
Escalate systematic issues to Adjudication/Clinical Review (definition gaps, ambiguous classes, recurring edge cases).
Deliverables (what you produce weekly)
QA audit reports (sample size, findings, severity distribution, root-cause categories)
Gate status + release checklist sign-off recommendations
Rework queue and closure verification
Trend insights and corrective action plan (top 3 issues + fixes)
Requirements
3–7+ years in data QA / annotation QA / operations quality; experience auditing labeled datasets (video preferred).
Strong command of sampling-based QA: stratified sampling, acceptance thresholds, and audit scoring.
High attention to detail; comfortable reading and enforcing detailed SOPs/guidelines.
Strong documentation skills; can write clear defect descriptions and rework instructions.
Comfortable with dashboards/spreadsheets; basic metric literacy (defect density, rework, throughput).
Note- Please apply via our official careers portal only, as applications sent directly to executives may not be considered.
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