Quality Control Technician III- Quality Control

Teva Global Business Services; Chennai District; On-site; INR 450,000 - 700,000; Full time

Job summary

Teva Global Business Services in Chennai seeks an analytical scientist to operate physical testing instruments, ensure GLP/GDP compliant data, and maintain instrument performance. The role involves hands-on HPLC, dissolution testing, water systems, and Empower 3.

You will interpret data, document results, and support training and safety practices. The position offers growth in a pharmaceutical quality environment.

Qualifications

• 2 to 5 years of hands-on experience in physical testing.
• Experience with HPLC, dissolution testing, water systems and Empower 3.
• Strong data interpretation and documentation skills under GLP/GDP.

Responsibilities

• Operate, maintain and troubleshoot physical testing instruments to ensure optimal performance.
• Conduct physical testing for stability samples and ensure compliance with GLP/GDP.
• Interpret data and document analytical activities with accuracy and integrity.
• Report interpreted results and alert supervisor of any anomalies in a timely manner.
• Ensure safe laboratory practices including PPE use and safety training completion.

Skills

HPLC

Dissolution testing

Water systems

Data interpretation

Documentation

PPE implementation

Education

M.Sc/M.Pharm/B.Pharm

Tools

Empower 3

Job description

Role & responsibilities

• Responsible for ensuring the handling, operation, and maintenance of instruments pertaining to physical testing to ensure optimal performance.
• Hands on experience on HPLC, dissolution testing, water systems, Empower 3.
• Responsible for conducting and ensuring physical testing relevant to the specification for all stability samples.
• Interpreting the data generated and ensuring proper documentation of all analytical activities in compliance with GLP/GDP requirements.
• Reporting interpreted data in line with specifications, compliance, and regulatory standards, and maintaining data integrity throughout the analytical lifecycle.
• Evaluation of reported results and reporting any abnormal results to the supervisor on time.
• Handling of laboratory software.
• Ensuring the use of safety apparel and PPEs while working in the laboratory.
• Ensuring timely completion of assigned training.

Qualification:

• 2 to 5 years
• M.Sc/M.Pharm/ B.Pharm