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Prayagraj, India Good People HR Pty Ltd Full timeQuality and Environmental Co-ordinator to progress into a Quality Manager role Seeking: Quality and Environmental Co-ordinator to progress into a Quality Manager roleIndustry: Defence / Project ManufacturingLocation: SE SuburbsPurpose of the role: Coordinate the Internal Audit program. Coordinate the Corrective and Preventive Action System. Assist in...
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Prayagraj, India Good People HR Pty Ltd Full timeSeeking: Quality and Environmental Co-ordinator to progress into a Quality Manager role Seeking: Quality and Environmental Co-ordinator to progress into a Quality Manager role Industry: Defence / Project Manufacturing Purpose of the role: Coordinate the Internal Audit program. Coordinate the Corrective and Preventive Action System. Assist in coordinating the...
Quality assurance auditor
4 weeks ago
Job 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 requirements.Key Responsibilities:Conduct audits of clinical research sites across phases I–IV.Review CRFs, informed consent forms, and regulatory documents.Identify and report audit findings; recommend corrective actions.Support site staff with compliance guidance and training.Prepare audit reports and follow up on CAPA implementation.Qualifications:Bachelor’s degree in life sciences, nursing, pharmacy, or related field.10-12 years of clinical research experience, with auditing and QA experience.Knowledge of GCP, ICH guidelines, and FDA/EMA regulations.Strong communication, analytical, and organizational skills.Ability to travel is required.Preferred:Clinical Research or Quality Auditing certification (ACRP, SOCRA).Experience with e TMF and EDC systems.Experience auditing multi-center or global trials.Working Conditions:Up to 50% travel to clinical sites.Combination of remote, and field work.Flexible schedule to accommodate site audits.
