Quality Control Technician III- Quality Control

Teva Pharmaceuticals; Chennai District; On-site; INR 600,000 - 900,000; Full time

Job summary

Teva Pharmaceuticals is seeking a qualified analyst to manage the handling, operation and maintenance of instruments used for physical testing to ensure peak performance. The role involves hands-on HPLC, dissolution testing and work with water systems and Empower 3.

You will conduct physical testing on stability samples, interpret results, document activities per GLP/GDP standards and report data in line with regulatory requirements.

Qualifications

• 2 to 5 years of experience in physical testing or analytical labs.
• M.Sc/M.Pharm/ B.Pharm degree required or equivalent qualification.

Responsibilities

• Ensures handling, operation and maintenance of physical testing instruments for optimal performance.
• Performs HPLC and dissolution testing, maintains water systems, and uses Empower 3.
• Conducts physical testing for stability samples and ensures results meet specifications.
• Interprets data and documents analytical activities in compliance with GLP/GDP requirements.
• Reports interpreted data aligned with specifications, compliance and regulatory standards.
• Evaluates reported results and flags any abnormalities to supervisor in a timely manner.
• Handles laboratory software and ensures proper use of PPE and safety protocols.
• Completes assigned training on time and maintains safety standards.

Skills

HPLC

Dissolution testing

Empower 3

Data interpretation

Education

M.Sc/M.Pharm/ B.Pharm

Tools

Water systems

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