Executive – Quality Assurance Jobs in Raptim Research Pvt. Ltd - Navi Mumbai, Maharashtra
Raptim Research Pvt. Ltd.
Navi Mumbai, Maharashtra, India
Posted on 19-01-2026
1 Vacancy
Description
- Job Title: Executive – Quality Assurance
- Qualification: BPharm/Mpharm
- Location: Raptim Research Pvt. Ltd - Navi Mumbai, Maharashtra
- Work Experience: 0 to 2 Years
Job Description
- Monitor day-to-day operations to ensure compliance with quality standards and SOPs.
- Conduct routine quality checks, inspections and process monitoring activities.
- Maintain quality documents, logs and records in an accurate and timely manner.
- Identify non-conformities and assist in implementing corrective and preventive actions (CAPA).
- Support internal and external quality audits and regulatory inspections.
- Coordinate with cross-functional teams to improve process quality and operational efficiency.
- Ensure adherence to ISO / NABH / GMP / GCP guidelines and organizational quality policies.
- Prepare quality reports, checklists and compliance documentation.
- Assist in training staff on quality procedures and standards.
- Participate in continuous improvement initiatives and quality assurance programs.
Take this opportunity to join Raptim Research Pvt. Ltd - Navi Mumbai, Maharashtra as a Executive – Quality Assurance in Navi Mumbai, Maharashtra and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.
Category
Pharmaceuticals
Preferred Education
Key Skills
About Organization
Raptim Research Pvt. Ltd. is a global independent Clinical Research Organization (CRO) headquartered in Navi Mumbai, Maharashtra, providing end-to-end clinical development, bioequivalence, bioanalytical, and trial management services for pharmaceutical and biotech companies worldwide. It operates state-of-the-art clinical research facilities in Mumbai and Gandhinagar with regulatory-compliant infrastructure supporting Phase I–IV trials across multiple therapeutic areas. The company’s core focus is on delivering high-quality, globally regulated clinical research services, accelerating drug development with strong quality and compliance standards. The Clinical Research Associate (CRA) role typically involves monitoring clinical trial sites, ensuring adherence to protocols and Good Clinical Practice (GCP), and supporting documentation and regulatory compliance.
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