Officer – 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: Officer – Quality Assurance
- Qualification: BSC Nusing
- Location: Raptim Research Pvt. Ltd - Navi Mumbai, Maharashtra
- Work Experience: 0 to 2 Years
Job Description
- Ensure daily operations comply with quality standards, SOPs and regulatory requirements.
- Perform routine quality checks, inspections and process audits.
- Maintain and update quality documents, records and reports accurately.
- Identify deviations and support corrective and preventive actions (CAPA).
- Assist in internal and external audits and regulatory inspections.
- Coordinate with departments to improve process quality and efficiency.
- Monitor adherence to ISO / NABH / GMP / GCP guidelines and company policies.
- Prepare quality performance reports, checklists and compliance summaries.
- Support training programs on quality standards and procedures.
- Promote continuous improvement and quality assurance best practices.
Take this opportunity to join Raptim Research Pvt. Ltd - Navi Mumbai, Maharashtra as a Officer – 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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