Junior Associate Job Details

Job Title: Junior Associate

Posting Start Date: 6/26/26

Job Description:

Company Overview

Role Purpose

The Team Member – QA – DP ensures that all drug product manufacturing activities are performed in compliance with Good Manufacturing Practices (GMP), company procedures, and regulatory standards. This includes line clearance, in-process verification, batch record review, deviation reporting, and documentation oversight during production operations. The role plays a critical part in ensuring product quality and batch release readiness, and in maintaining a state of regulatory compliance across the manufacturing floor.

Academic Stream

0

Work experience (in months)

0

Job Responsibility and key Decisions

Perform line clearance and areaequipment status checks before manufacturing operations begin.

Provide realtime onfloor QA oversight during manufacturing, packaging, and inprocess testing.

Review batch manufacturing records BMRBPR, ensuring completeness and correctness.

Verify compliance with SOPs, manufacturing instructions, and inprocess control limits.

Report and document any nonconformities or deviations observed during operations.

Support QA team in investigation and documentation of deviations, CAPAs, and change controls.

Ensure that materials, equipment, and documents are traceable and appropriately labeled.

Assist in the review of logbooks, cleaning records, temperaturehumidity monitoring logs, etc.

Perform QA checks related to label reconciliation, line clearance after packaging, and proper disposal of rejected material.

Support regulatory inspection readiness by ensuring documentation and shop floor conditions are auditcompliant.

Participate in GMP training sessions and stay current with qualityrelated SOPs and policies.

Confirm acceptability of batch record entries, equipment logs, and status labeling.

Decide whether to allow progression to the next step of manufacturing based on compliance checks.

Escalate deviations, discrepancies, or quality risks observed in real time.

Recommend corrections or clarifications to documentation before batch review is finalized.