Job Title: Assistant Manager – IPQA
Company: Lambda Therapeutic Research Ltd.
Location: Ahmedabad, India
Req ID: 1466
Work Location Type: On Site
Category: Quality Assurance / Manufacturing
Date Posted: Mar 08, 2026
Salary: ₹10,00,000 – ₹15,00,000 per year
Job Overview
The Assistant Manager – IPQA (In-Process Quality Assurance) is responsible for ensuring that manufacturing and quality operations comply with established Quality Management Systems (QMS) and Good Manufacturing Practice (GMP) standards. The role involves reviewing batch documentation, monitoring shop floor activities, supporting investigations, and coordinating cross-functional teams to maintain compliance and operational excellence within the manufacturing environment.
Key Responsibilities
Review batch manufacturing records, log books, and documentation formats including line clearance, sampling formats, and batch review sheets.
Review documentation maintained by Warehouse, Production, and Engineering teams to ensure accuracy and compliance.
Ensure proper documentation of Quality Assurance activities and adherence to online documentation systems.
Follow incident reporting systems and document deviations in accordance with established procedures.
Ensure availability and adherence to approved standard operating procedures (SOPs) for the manufacturing team.
Monitor compliance with Quality Management System elements including change control, incident management, and CAPA processes.
Verify that manufacturing facilities maintain Good Manufacturing Practice (GMP) standards, including environmental conditions, facility upkeep, material segregation, and labeling practices.
Support supervisors in investigations related to complaints, batch failures, OOS/OOT results, and operational incidents.
Conduct root cause analysis, collect supporting data, and coordinate investigations with cross-functional teams.
Document corrective and preventive actions (CAPA), ensure timely implementation, and monitor effectiveness.
Assist in internal and external audit activities by preparing documentation and providing necessary information during audits.
Track audit responses from user departments and ensure closure of audit action items within defined timelines.
Required Skills and Competencies
Strong understanding of Quality Management Systems (QMS) and Good Manufacturing Practices (GMP).
Experience with batch documentation review and shop floor QA oversight.
Knowledge of deviation management, CAPA processes, and change control systems.
Strong analytical and root cause analysis capabilities.
Effective cross-functional collaboration with production, engineering, and warehouse teams.
Attention to detail and strong documentation management skills.
Familiarity with regulatory compliance requirements in pharmaceutical manufacturing.
Experience
7+ years of industrial experience in Manufacturing, Quality Control, Quality Assurance, or Engineering & Development within the pharmaceutical or biotechnology industry.
Educational Qualifications
B.Pharm, or
Postgraduate degree in Microbiology, Quality Assurance, Biochemistry, Biotechnology, or a related field.
Equal Opportunity Statement
Lambda Therapeutic Research Ltd. is committed to providing equal employment opportunities to all qualified candidates and fostering an inclusive work environment. Applicants will be considered without regard to race, gender, religion, nationality, disability, or other protected characteristics.
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