Are you looking to kickstart your career in pharmaceutical regulatory documentation or quality assurance? Labcorp, a global leader in life sciences, is offering an exciting Intern – Controlled Docs Coordinator position in Bangalore, India.
This opportunity is perfect for graduates passionate about clinical documentation control, GxP compliance, and regulatory operations, looking to build a strong foundation in pharma quality systems.
🧾 Key Responsibilities
As an Intern – Controlled Docs Coordinator, you will:
- Follow departmental Standard Operating Procedures (SOPs) and Work Instructions.
- Complete all required trainings within set timelines.
- Manage and maintain controlled documents ensuring timely access for end users.
- Maintain and track document inventory and ensure data integrity.
- Perform quality checks to verify document accuracy and compliance.
- Escalate issues affecting document release and support timely resolution.
- Ensure Regulatory Compliance and Quality Assurance (RC&QA) standards are upheld.
- Support additional tasks as assigned by management.
🎓 Qualifications & Eligibility
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, or related disciplines.
- Strong understanding of Good Documentation Practices (GDP).
- Excellent attention to detail and organizational skills.
- Proficiency in MS Office and familiarity with document management systems.
- Good communication and teamwork abilities.
💼 Benefits of Joining Labcorp
- Gain hands-on experience in controlled documentation and regulatory compliance.
- Work in a global, innovation-driven environment.
- Opportunity to learn from industry experts and build your professional network.
- Potential career growth within Labcorp’s regulatory and quality departments.
📝 Application Details
