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Life Sciences QA Jobs at OrBion Pharmaceuticals Pvt Ltd
Looking to build a strong career in pharmaceutical quality assurance? Life Sciences QA Jobs at OrBion Pharmaceuticals Pvt Ltd are now open for skilled professionals seeking growth in one of India’s fastest-advancing pharma hubs. With opportunities in Analytical Quality Assurance (AQA) and documentation-based QA roles, OrBion offers a dynamic work environment, hands-on exposure to regulated workflows, and excellent career progression for candidates with Life Science or Pharmacy qualifications.
Company – OrBion pharmaceuticals
Job role – Quality Assurance (Documentation) Females preferred (1-3) exp
Location – Chennai, Tamil Nadu
Interview Mode – Telephonic interview and direct interview for 2nd round
Experience – 1–3 years
Qualifications – B.Sc / M.Sc / B.Pharm / M.Pharm or any Life Science/Pharmacy background.
1–3 years of proven experience in QA Documentation within a pharma or biotech setup.
Work Mode – On-site
Salary – Salary according to expertise and experience
Educational Qualification – B.Sc / M.Sc / B.Pharm / M.Pharm or any Life Science/Pharmacy background.
Job Summary:
The QA (Documentation) professional will be responsible for managing, reviewing, controlling, and maintaining all quality-related documents in compliance with regulatory standards. The role ensures the accuracy, completeness, and traceability of GMP documentation and supports audits, SOP compliance, and overall quality systems within the organization.
Key Responsibilities –
A. Documentation Management
• Prepare, review, issue, and control GMP documents such as SOPs, STPs, BMRs, BPRs, specifications, and logbooks.
• Maintain Document Control System (DCS) and ensure timely revision, archival, and distribution of documents.
• Coordinate issuance of controlled copies to respective departments and track real-time documentation status.
B. Record & Data Control
• Ensure proper maintenance of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
• Review analytical reports, testing records, and QA checklists for completeness and compliance.
• Manage master documents and ensure alignment with regulatory guidelines and internal SOPs.
C. Change Control & Compliance
• Support the creation, tracking, and closure of Deviation, Change Control, CAPA, and incident records.
• Ensure all documentation complies with GMP, GLP, ALCOA+ principles, and company quality standards.
• Assist in ensuring all updates are executed systematically and documented clearly.
Stages of the interview may include:
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Telephonic round
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Come down for the direct face-to-face
