Job Description
Job Title:  ASSOCIATE MANAGER
Posting Start Date:  4/6/26
Job Description: 

Company Overview

Role Purpose

The Team Member – QA – DS is responsible for executing day-to-day quality assurance activities related to the manufacture of drug substances (APIs), including line clearance, in-process verification, batch record review, deviation support, and GMP compliance monitoring. The role ensures that manufacturing operations are conducted in accordance with applicable SOPs, regulatory guidelines, and internal quality systems to maintain the quality, safety, and compliance of drug substance production.

Academic Stream

0

Work experience (in months)

0

Job Responsibility and key Decisions

Perform line clearance checks before the start of batch manufacturing or equipment use.

Monitor critical steps during DS manufacturing, ensuring adherence to batch records and procedures.

Review inprocess documents, logbooks, and production records for accuracy and completeness.

Support QA review of executed Batch Manufacturing Records BMRs for compliance and release readiness.

Participate in deviation investigations, support root cause analysis and documentation.

Perform QA verification of cleaning activities, including checks on cleaning status and record accuracy.

Assist in label issuance and reconciliation of materials, intermediates, and final product.

Ensure logbooks, temperaturehumidity records, and equipment usage records are maintained properly.

Escalate any observed noncompliance or procedural deviation immediately to QA leads.

Support training compliance by maintaining awareness of updated SOPs and attending required sessions.

Assist in selfinspection readiness and audit documentation preparation.

Verify and confirm line clearance and inprocess observations.

Recommend batch record corrections or clarifications before review is finalized.

Escalate deviations, discrepancies, or nonconformances during manufacturing.

Suggest procedural or documentation improvements within scope of operations.