QA Job at Syngene | CTM QA Auditor Role | Pharma Eligible
Looking for a Pharma QA Job in clinical research? Syngene Careers is hiring a CTM QA Auditor in Bangalore. This opportunity is ideal for B.Pharm, M.Pharm, M.Sc., and life sciences graduates who want to build a career in Clinical Trial Quality Assurance, GCP compliance, and regulatory audits.
- Job Title: CTM QA Auditor
- Department: Clinical Trial Management – Quality Assurance
- Location: Bangalore, Karnataka
About The Company
Syngene Careers offers exciting opportunities for professionals seeking a Pharma QA Job in clinical research and quality assurance. As a leading contract research, development, and manufacturing organization (CRDMO), Syngene provides exposure to global clinical trials, international regulatory standards, and advanced quality systems while enabling professionals to contribute to innovative healthcare solutions.
Job Description
This Pharma QA Job at Syngene Careers focuses on ensuring that clinical trial processes, documentation, and systems comply with regulatory requirements, Good Clinical Practice (ICH-GCP), and internal quality standards. The selected candidate will conduct internal and investigator site audits, review clinical trial documentation, identify compliance risks, and support CAPA implementation to maintain the highest quality standards across clinical trials. The role also involves collaborating with Clinical Operations, Data Management, Regulatory Affairs, and Compliance QA teams, facilitating sponsor and regulatory inspections, maintaining QA systems, preparing audit reports, and supporting continuous quality improvement initiatives. Candidates should be willing to travel for site audits as required.
Key Responsibilities
- Conduct internal and clinical site QA audits.
- Ensure compliance with ICH-GCP, GxP, SOPs, and study protocols.
- Identify quality risks and implement CAPA.
- Prepare and review audit reports.
- Support sponsor audits and regulatory inspections.
- Monitor audit findings and follow-up actions.
- Maintain QA documentation and audit systems.
- Collaborate with Clinical Operations, Data Management, and Regulatory teams.
Eligibility Criteria
- Education: B.Pharm, M.Pharm, M.Sc., or Any Graduate
- Experience: Experienced candidates with knowledge of clinical trial quality assurance and regulatory compliance.
Required Skills
- Clinical Trial Quality Assurance
- ICH-GCP & GxP Compliance
- Clinical Site Auditing
- CAPA & Risk Assessment
- CTMS & Electronic Data Capture (EDC)
- Regulatory Inspections & Documentation
- MS Office & QA Systems
- Communication & Cross-functional Collaboration
Why Join Syngene?
If you’re searching for a Pharma QA Job, Syngene Careers offers an excellent platform to build expertise in clinical quality assurance, regulatory compliance, and global clinical trial auditing. You’ll work with experienced professionals, support international clinical studies, and gain valuable exposure to sponsor audits, regulatory inspections, and quality management systems.
