Job Description
Job Title:  EXECUTIVE
Posting Start Date:  6/22/26
Job Description: 

Company Overview

Role Purpose

The Team Member – Quality – QC – In Process is responsible for conducting in-process quality control activities during the manufacturing of pharmaceutical products. This includes performing tests and inspections on materials, components, and products at various stages of the production process to ensure compliance with quality standards and regulatory requirements. The role involves maintaining accurate records, analyzing results, and collaborating with production teams to resolve quality issues. The team member supports the identification and correction of any deviations, ensuring that the final product meets the required specifications for safety, efficacy, and quality.

Academic Stream

0

Work experience (in months)

0

Job Responsibility and key Decisions

Perform Routine InProcess Testing

Conduct sampling and testing of production batches at defined stages.

Ensure results meet specified limits and notify supervisors immediately if outofspecification OOS results occur.

Documentation and Reporting

Accurately document test results and sampling details in batch records.

Report data promptly to Production and QA teams for batch decisions.

Maintain Testing Area and Equipment

Keep the inprocess QC lab area clean and organized.

Perform routine equipment checks and escalate maintenance needs.

Adhere to SOPs and GMP

Follow all applicable SOPs, GMP guidelines, and safety protocols strictly.

Participate in quality trainings and refreshers.

Support Deviation and CAPA Processes

Provide information and support for investigations related to inprocess testing deviations.

Implement corrective and preventive actions as instructed.

Assist in Continuous Improvement

Suggest improvements in sampling and testing procedures.

Participate in quality initiatives within the QC or production area.

DecisionMaking Scope

Make routine decisions related to sample handling and minor troubleshooting within SOP limits.

Escalate any critical quality or compliance issues to Team Lead or QC Manager.