Advertisement
SafeVig Solutions Pvt Ltd, a global technology-enabled CRO specializing in Pharmacovigilance, Clinical Data Management, and Regulatory Affairs, is expanding its Hyderabad office. We are seeking an experienced QA Associate/Executive to strengthen our Quality Management Systems (QMS) and ensure compliance with global standards, including ICH-GCP, GVP, FDA, EMA, and CDSCO. This is a unique opportunity to contribute to a fast-growing, innovation-driven organization shaping the future of clinical and pharmacovigilance services.
Key Responsibilities
- Implement, maintain, and monitor Quality Management Systems (QMS) across clinical operations.
- Conduct internal and vendor audits to ensure regulatory compliance and manage CAPA (Corrective and Preventive Actions).
- Ensure SOP adherence, regulatory compliance, and preparation for inspections.
- Support continuous process improvements and compliance initiatives within clinical services.
- Collaborate with cross-functional teams to uphold global GXP standards.
Qualifications & Skills
- Educational Qualification: Life Sciences, Pharmacy, or Clinical Research degree.
- Experience: 4-5 years in QA within CRO/Pharma/PV environments.
- Strong knowledge of GXP, CAPA, and QMS.
- Excellent communication, analytical, and documentation skills.
- Ability to work in a fast-paced, quality-driven environment.
Why Join SafeVig?
- Be part of a rapidly growing, innovation-driven CRO.
- Gain hands-on experience in global pharmacovigilance and clinical operations.
- Work in a collaborative, learning-focused environment.
- Contribute to quality excellence and regulatory compliance at a global scale.
How to Apply
Send your CV to support@safevigsolutions.com
Subject: Application – QA (Clinical Services)
Advertisement
