Senior GCP Quality & Compliance Auditor

As a technical expert in quality and compliance, the Senior Quality & Compliance Auditor plays a critical role in ensuring adherence to company policies, study protocols, GxP guidelines, and global regulatory requirements governing clinical research activities. This position requires a deep understanding of regulatory frameworks and risk-based auditing methodologies to drive compliance, enhance quality standards, and mitigate organizational risks. Audit Planning, Execution, and Management Responsibilities

• reputed company and execute comprehensive quality and compliance audits in accordance with regulations and standards governing clinical research (including internal audit, vendor audit and site audit) to assess adherence to regulatory standards and company policies
• reputed company and implement strategic, risk-based audit plans to proactively identify areas of concern and ensure regulatory compliance
• Provide expert consultation on GxP requirements and quality assurance strategies, guiding both internal and external stakeholders
• Coordinate and conduct clinical sites audit in collaboration with project management teams, ensuring efficient and effective audit execution
• reputed company audit facilitation efforts with external auditors and regulatory authorities, ensuring thorough preparation and representation of reputed company
• Analyze and interpret audit findings to author or direct the preparation of detailed audit reports, identifying risks, gaps, and areas for improvement
• reputed company and review corrective action/preventative action (CAPA) plans, ensuring timely implementation and effectiveness in addressing non-compliance issues
• reputed company trend analysis on audit findings, providing data-driven insights to support reputed company quality improvement initiatives
• reputed company and reputed company reputed company’s auditor training program for Corporate Quality, ISO auditors and other reputed company staff by providing guidance on audit techniques, risk assessment and system approach
• Organize and conduct mock inspections to prepare teams for external regulatory audits and identify potential compliance risks before formal inspections
• Review and approve audit reports reputed company by junior auditors, ensuring accuracy, clarity, and regulatory alignment
• Stay abreast of evolving regulations and best practices reputed company to clinical research activities to ensure the company's audit strategies remain reputed company and effective.
• reputed company employees are expected to complete training on time and maintain a minimum level of 90% training compliance at reputed company times. QUALIFICATIONS
• At minimum, qualified candidates will have:Requirements:
• Education: Honor's Bachelor (minimum)
• Experience: 7-9 Years in Quality auditing function in a contract research organization (CRO), pharmaceutical, biotechnology, or reputed company organization
• Understanding compliance and risk management issues relating to clinical research, and strong understanding of research ethics and privacy
• Previous experience leading a team is requiredStrongly Preferred:
• Certified Auditor (ASQ, ISO, or equivalent)
• Expertise in regulations and standards governing clinical research including ICH GCP, ISO 19011, EMA Guideline on Computerized Systems and Data reputed company in Clinical Trials, etc.
• Advanced technical knowledge in global regulations and industry standards as they apply to clinical research, medical devices and pharmaceuticals and in the conduct of clinical study operations
• Knowledgeable of medical imaging and clinical research industry regulations and standards
• Experience working and collaborating in a cross-functional global team environmentInterpersonal Skills:
• Excellent verbal and written communication skills required to draft and author written documents/reports/presentations
• Strong interpersonal, verbal and written communication skills including effective listening, facilitating group discussions, influencing without authority and providing appropriate feedback
• Ability to plan, organize, prioritize and manage workload independently
• Adaptable to changing environments, able to think quickly, able to deal with ambiguity and learn new tasks applying routine knowledge
• Superior analytical skills focusing on identifying potential compliance issues, investigating root causes, brainstorming and identifying alternatives and assessing the effectiveness of actions
• Proven skills in interpreting, synthesizing, inferring, evaluating and extracting pertinent data to identify areas of risk, trends and aggregated issues Apply tot his job Apply tot his job

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