Company: Labcorp
Job Title: Quality Reviewer I
Location: Bangalore
Job Type: Full-Time
Work Mode: On-Site
Industry: Clinical Research | Pharmacovigilance | Regulatory Compliance | Pharmaceutical Industry
Experience Required: 2+ Years
Eligible Candidates: Life Sciences Graduates, Pharmacy Graduates, Medical Science Professionals, Clinical Research Professionals
About Labcorp
Labcorp is a globally recognized healthcare and life sciences organization committed to advancing scientific innovation and improving patient health outcomes worldwide. The company offers outstanding career opportunities for professionals looking to build expertise in clinical research, regulatory compliance, quality review, and pharmaceutical operations.
Labcorp is currently hiring for the position of Quality Reviewer I at its Bangalore office. This opportunity is ideal for candidates with experience in quality review, clinical trial processes, medical technology, or pharmaceutical operations who are seeking long-term growth in the healthcare and life sciences industry.
Job Overview
The Quality Reviewer I will be responsible for performing quality checks, ensuring regulatory compliance, identifying process gaps, supporting CAPA activities, and contributing to continuous process improvement initiatives within the operational team.
This role requires strong analytical skills, attention to detail, problem-solving capabilities, and the ability to work collaboratively in a regulated healthcare environment.
Key Responsibilities
Follow departmental Standard Operating Procedures (SOPs) and Work Instructions consistently.
Perform Quality Check (QC) reviews for assigned operational tasks and provide timely feedback to associates and reporting managers.
Assist the QC Lead in preparing QC trend analysis reports and maintaining escalation trackers.
Identify process gaps, compliance issues, and quality deviations while recommending corrective actions.
Support teams in preparing CAPA (Corrective and Preventive Action) documentation for QC observations.
Ensure adherence to internal quality standards and regulatory compliance requirements.
Monitor customer complaints, operational issues, and support resolution management.
Participate in continuous improvement initiatives and process optimization activities.
Understand client-specific requests and service requirements across different operational clusters.
Manage operational issues independently while escalating complex concerns appropriately.
Collaborate effectively with internal teams to maintain workflow accuracy and efficiency.
Eligibility Criteria
Minimum Qualification
Bachelor’s Degree in Life Sciences, Pharmacy, Medical Sciences, Biotechnology, Clinical Research, or related healthcare discipline.
Preferred Qualification
Candidates with the following background will be preferred:
2+ years of experience in:
Quality Review Environment
Clinical Trial Operations
Pharmaceutical Industry
Medical Technology
Regulatory Compliance
Clinical Research Operations
Required Skills
Strong knowledge of quality review and compliance processes
Understanding of clinical trial and pharmaceutical industry workflows
Excellent analytical and problem-solving abilities
Strong planning and organizational skills
Ability to work collaboratively within cross-functional teams
High attention to detail and documentation accuracy
Knowledge of CAPA processes and QC trend analysis
Proficiency in Microsoft Office tools including:
MS Word
MS Excel
Windows Applications
Work Schedule
40 Hours per Week
Monday to Friday
Rotational Shift Schedule
Why Join Labcorp?
Opportunity to work with a globally recognized healthcare organization
Exposure to international quality and compliance standards
Career growth opportunities in clinical research and regulatory operations
Collaborative and innovation-driven work culture
Continuous learning and professional development opportunities
Equal Opportunity Employer
Labcorp is an Equal Opportunity Employer committed to diversity, inclusion, and workplace belonging. All qualified applicants will receive fair consideration regardless of race, religion, gender, disability, age, sexual orientation, or any other legally protected characteristic.
The organization encourages applications from professionals across diverse backgrounds and experiences.
Who Should Apply?
This role is highly suitable for:
Pharmacovigilance Professionals
Clinical Research Associates
Quality Assurance Executives
Regulatory Affairs Professionals
Life Sciences Graduates with QC experience
Pharmaceutical Industry Professionals seeking compliance-focused roles
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