Company Description ICBio Clinical Research is a Contract Research Organization (CRO) focused on using science to advance human health and wellbeing. The organization partners with physicians, drug developers, hospitals, medical researchers, and patients to address a wide range of health challenges, from improving diagnostic testing to supporting new pharmaceutical launches.

ICBio leverages extensive scientific expertise and data-driven insights to provide reliable information for informed health decisions. The company holds approvals from DCGI, CDSCO, MOH Kazakhstan, and operates a NABL-accredited central laboratory with LIMS. ICBio has completed studies for regulatory authorities across multiple countries, including India, the Philippines, Tanzania, Vietnam, Kazakhstan, and other CIS nations.

Role Description The QA Manager is a full time, on-site role based in Bengaluru, responsible for overseeing quality assurance activities across clinical research projects. This role includes developing, implementing, and maintaining QA systems and SOPs in compliance with applicable regulatory and GCP guidelines.

The QA Manager will plan and conduct internal and external audits, manage CAPA processes, and monitor adherence to quality standards in clinical operations, data management, laboratory procedures, and documentation. The role also involves training teams on quality requirements,



coordinating with cross-functional stakeholders to resolve quality issues, and preparing reports and metrics for senior leadership and regulatory inspections. The QA Manager will support continuous improvement initiatives to strengthen quality culture and ensure inspection readiness at all times.

Qualifications

- Strong background in clinical research quality assurance, including GCP, regulatory compliance, and QA system implementation.
- Experience in planning and conducting audits of sites, laboratories, vendors, and internal functions, with effective CAPA management.
- Proficiency in documentation control, SOP development, and oversight of LIMS or similar quality-related systems.
- Ability to train and mentor teams on quality standards, risk management, and best practices in a CRO or clinical research environment.
- Excellent analytical, problem-solving, and communication skills, with attention to detail and a structured approach to reporting.
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine, or a related field; advanced QA or clinical research certifications are an advantage.
- Prior experience in a QA leadership or managerial role within a CRO, pharmaceutical company, or clinical research setting.
- Comfort working on-site in Bengaluru and collaborating with cross-functional and international stakeholders.

📌 Qa Manager (Bengaluru)
🏢 ICBio Clinical Research: CRO
📍 Bengaluru