DEPUTY MANAGER Job Details

Job Title: DEPUTY MANAGER

Posting Start Date: 6/18/26

Job Description:

Company Overview

Role Purpose

The Team Member – MES QA is responsible for supporting the quality assurance activities related to the Manufacturing Execution System (MES) within the pharmaceutical manufacturing facility. This role ensures that the MES operates in compliance with regulatory requirements, company standards, and quality policies. The team member assists in validating, monitoring, and maintaining the integrity of the MES to facilitate accurate, reliable, and compliant manufacturing processes.

Academic Stream

0

Work experience (in months)

0

Job Responsibility and key Decisions

Support the QA team in the validation and qualification of MES software and related systems.

Execute test scripts and protocols to ensure MES functionality meets quality and regulatory requirements.

Review MESgenerated data for accuracy, consistency, and compliance with data integrity standards.

Assist in investigating MESrelated issues or deviations and participate in root cause analysis.

Maintain detailed documentation of validation activities, test results, and quality reports.

Collaborate with IT, production, and quality teams to support MESrelated change controls and system upgrades.

Participate in internal and external audits related to MES compliance.

Support training activities for endusers on MES quality practices and compliance requirements.

Monitor MES performance and compliance under guidance to ensure continuous improvement.

Ensure adherence to company SOPs and quality standards during all MES QA activities.

Key Decisions

Identifying and reporting MES quality issues or deviations to supervisors or QA leads.

Recommending improvements in MES QA processes based on observations and analysis.

Participating in decisions regarding validation and testing outcomes under supervision.

Escalating critical compliance or data integrity concerns to higher management.