Tech Observer
Manager QA (Clinical Trials)
Skills
1 month ago
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Important information
Contract type:
Permanent
Location:
Mumbai, Maharashtra, India
Work mode:
Hybrid
Published on:
14 October 2026
What they need
Job highlights
- Experience in Quality Assurance systems in Clinical Research/CRO/Pharma with expertise in document control and quality document lifecycle management
- Manage document control, formatting, version control, and lifecycle of quality documents
Strong knowledge of Quality Assurance systems within Clinical Research /
CRO / Pharma environments.. Experience in document control, formatting, version control and lifecycle
management of quality documents. etc
Required Candidate profile
Good Communication;Knowledge of ISO 9001, ISO 14155, ISO 27001, GCP, and applicable
regulatory quality standards will be an added advantage
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