Ex-fda Auditor
1 week ago
Our client is seeking an Ex-FDA Auditor for a facilities audit project for an API organization in India. This is a complete facility audit covering their QA/QC/Engineering departments and all their documentation. This is a pre-approved USFDA facility located in India.
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Senior QA Auditor/ Senior GCP Auditor
2 weeks ago
India Tilda Research Full timeRemote: India Open to candidates with experience in global clinical research operations. About the Role We are seeking a Senior QA Auditor/ Senior GCP Auditor professional with proven experience in audits, SOP management, and regulatory compliance across global clinical research environments. This role is ideal for someone who has worked within or closely...
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Senior QA Auditor/ Senior GCP Auditor
2 weeks ago
India Tilda Research Full timeRemote: India Open to candidates with experience in global clinical research operations. About the Role We are seeking a Senior QA Auditor/ Senior GCP Auditor professional with proven experience in audits, SOP management, and regulatory compliance across global clinical research environments. This role is ideal for someone who has worked within or closely...
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Senior QA Auditor/ Senior GCP Auditor
2 weeks ago
India Tilda Research Full timeRemote: India Open to candidates with experience in global clinical research operations. About the Role We are seeking a Senior QA Auditor/ Senior GCP Auditor professional with proven experience in audits, SOP management, and regulatory compliance across global clinical research environments. This role is ideal for someone who has worked within or closely...
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Senior QA Auditor/ Senior GCP Auditor
2 weeks ago
India Tilda Research Full timeRemote: IndiaOpen to candidates with experience in global clinical research operations.About the RoleWe are seeking a Senior QA Auditor/ Senior GCP Auditor professional with proven experience in audits, SOP management, and regulatory compliance across global clinical research environments. This role is ideal for someone who has worked within or closely with...
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Sr. QA Auditor
2 weeks ago
India Tilda Research Full timeRemote: India Open to candidates with experience in global clinical research operations. We are seeking a Senior QA Auditor/ Senior GCP Auditor professional with proven experience in audits, SOP management, and regulatory compliance across global clinical research environments. This role is ideal for someone who has worked within or closely with a global...
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Quality Assurance Auditor
3 weeks ago
India K3-Innovations, Inc. Full timeJob Title: Clinical Quality Compliance ManagerLocation: Bengaluru, Karnataka, IndiaReports To: QA/Compliance Director or Clinical Operations DirectorJob Summary:Clinical Site Auditor to ensure compliance and quality at Clinical Trial sites. You will conduct site audits, review documentation, and verify adherence to protocols, GCP, GLP and regulatory...
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Quality Assurance Auditor
3 weeks ago
India K3-Innovations, Inc. Full timeJob Title: Clinical Quality Compliance Manager Location: Bengaluru, Karnataka, India Reports To: QA/Compliance Director or Clinical Operations Director Job Summary: Clinical Site Auditor to ensure compliance and quality at Clinical Trial sites. You will conduct site audits, review documentation, and verify adherence to protocols, GCP, GLP and regulatory...
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Quality Assurance Auditor
3 weeks ago
India K3-Innovations, Inc. Full timeJob Title: Clinical Quality Compliance Manager Location: Bengaluru, Karnataka, India Reports To: QA/Compliance Director or Clinical Operations Director Job Summary: Clinical Site Auditor to ensure compliance and quality at Clinical Trial sites. You will conduct site audits, review documentation, and verify adherence to protocols, GCP, GLP and regulatory...
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Quality Assurance Auditor
1 week ago
India K3-Innovations, Inc. Full timeJob Description Job Title: Clinical Quality Compliance Manager Location: Bengaluru, Karnataka, India Reports To: QA/Compliance Director or Clinical Operations Director Job Summary: Clinical Site Auditor to ensure compliance and quality at Clinical Trial sites. You will conduct site audits, review documentation, and verify adherence to protocols, GCP, GLP and...
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ISO 13485 Lead Auditor
1 day ago
India RQM+ Full time ₹ 20,00,000 - ₹ 25,00,000 per yearRQM+ is The MedTech CRO, accelerating innovation to patient impact. Our tailored solutions deliver regulatory and quality expertise, FDA-recognized laboratory services, clinical trials, and reimbursement strategies across device types and therapeutic areas to bring life-changing technologies to patients — faster, safer, better. We don't make MedTech. We...