Labcorp is hiring a Document Coordinator I in Bengaluru. This pharma jobs position in quality documentation is ideal for detail-oriented professionals seeking pharmaceutical careers in India in a global diagnostics and drug development leader.
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About the Company
Labcorp is a leading global life sciences company providing vital diagnostics, drug development, and healthcare innovation solutions. With nearly 70,000 employees across 100+ countries, Labcorp harnesses data and AI to deliver insights that improve health outcomes.
The company excels in regulatory compliance, innovation, and operational excellence, partnering with pharmaceutical companies, researchers, and healthcare providers to accelerate scientific progress and patient care worldwide.
Job Details
- Company Name: Labcorp
- Experience: 1–2 years in document management or related roles
- Qualification: Relevant educational background
- Location: Bengaluru, India
- Work Type: Hybrid (General Shift 9:00 AM – 6:00 PM)
Job Description
Labcorp is seeking a Document Coordinator I to support quality documentation processes at its Bengaluru facility. The role involves reformatting, reviewing, and managing controlled documents within the Veeva QualityDocs system. This position ensures accuracy, compliance, and timely processing of policies and Standard Operating Procedures (SOPs) in a regulated environment.
Document Coordinator I
- Department: Quality / Document Management
- Market: Pharmaceuticals / Life Sciences
- Role: Document Coordinator I
- Experience: 1–2 Years
- Education/Qualification: Relevant qualifications
Skills/Qualifications
- 1–2 years experience in document management or quality documentation
- Strong attention to detail and time management skills
- Proficiency in Microsoft Office (Word, Excel, PowerPoint)
- Experience with document management systems (Veeva Vault preferred)
- Knowledge of Quality Management Systems (QMS) and controlled processes
- Familiarity with GLP/GCP standards (advantage)
Key Responsibilities
- Reformat and prepare controlled documents per templates
- Review formatting for accuracy and compliance
- Manage documents in Veeva QualityDocs
- Collaborate with SMEs and QA teams for reviews and approvals
- Identify and escalate deviations from standards
- Maintain organized documentation practices
- Support quality and compliance initiatives
Benefits/Perks
- Career growth in global life sciences
- Learning opportunities in quality systems
- Hybrid work model with flexible timing
- Collaborative and inclusive work culture
- Contribution to healthcare innovation
How to Apply
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Labcorp career page.
🔗 Click below to apply directly for this job
Apply online through the Labcorp careers portal (job requisition ID 2618386). For more pharma jobs and quality roles in Bengaluru, visit Pharma Recruiter.
Why You Should Join
Labcorp offers a dynamic environment where data and AI drive meaningful impact on health outcomes. Employees benefit from long-term career stability, recognition for contributions, and opportunities to work on innovative solutions. Join a company committed to inclusion, excellence, and transforming patient care globally.
FAQs
Q1: What experience is needed for the Document Coordinator I role at Labcorp? A: 1–2 years in document management or related quality roles.
Q2: What is the work schedule and model? A: General shift (9:00 AM – 6:00 PM) with hybrid work arrangement in Bengaluru.
Q3: What systems will I work with? A: Veeva QualityDocs and Microsoft Office applications.
Q4: Why choose Labcorp for pharmaceutical careers? A: It provides global scale, innovation in diagnostics and drug development, and a supportive, inclusive culture.
