About the Role

Key Responsibilities

Perform raw material testing and analysis using chromatography and related laboratory techniques.

Support compliant material release decisions to ensure production readiness and uninterrupted supply.

Maintain accurate documentation and strong data integrity across testing and quality records.

Ensure full compliance with Good Manufacturing Practices and site quality standards.

Support investigations and quality issue resolution in a high-pressure manufacturing environment.

Collaborate with production, procurement, and suppliers to prevent delays and resolve risks.

Contribute technical expertise to inspection readiness and continuous improvement initiatives.

Essential Requirements

Bachelor’s degree in Pharmacy or a related scientific field.

At least two years of experience in pharmaceutical quality control.

Hands-on experience in raw material testing, including chromatography-based analysis.

Strong knowledge of Good Manufacturing Practices and quality compliance requirements.

High attention to data integrity, documentation accuracy, and reliable execution.

Ability to manage complexity, solve problems quickly, and collaborate across teams.

Desirable Requirements

Experience in environmental monitoring

Exposure to quality control, analytical science and technology, or quality assurance environments.

Desired Candidate Profile