Teva is hiring for the role of Quality Control Technician III at its Goa facility. The selected candidate will join the Nitrosamine team at the Watson Pharma Pvt. Ltd Goa Facility and contribute to analytical activities that support patient safety and regulatory compliance.

This role is suitable for candidates with hands-on experience in analytical method development and validation, especially in nitrosamine impurity testing for drug substance and drug product. The position involves laboratory work, instrument handling, documentation, compliance, and support for critical quality control studies.

Key Responsibilities

• Develop and validate analytical methods for nitrosamines-related activities using LCMS, GCMS and IC under guidance from senior team members.
• Manage samples received from different sites for the Nitrosamine project.
• Test samples for nitrosamines-related activities.
• Troubleshoot analytical instruments for difficulties faced during day-to-day operations.
• Support laboratory readiness by maintaining columns, standards, chemicals, spares, consumables and other prerequisites.
• Prepare analytical protocols, reports and technical documentation in compliance with regulatory standards.
• Conduct routine instrument operation, calibration and maintenance activities, and escalate issues for troubleshooting.
• Ensure accurate documentation of instrument usage, calibration records and compliance.
• Follow EHS guidelines and maintain safe laboratory practices.
• Maintain laboratory compliance and data integrity during daily operations.
• Participate in internal audits and contribute to readiness for external inspections.

Qualification

• M.Sc. in Chemistry or M.Pharm.
• Good knowledge of analytical chemistry, especially analytical method development and validation for nitrosamine impurities in drug substance and drug product.
• Ability to conduct literature searches for development of analytical methods.
• Familiarity with computerized systems such as TrackWise and Veeva Vault.
• Experience in cGMP/GLP environments and regulatory-compliant documentation.
• Sound knowledge of pharmaceutical quality systems and ICH guidelines.
• Strong attention to detail and ability to work effectively in a team setting.
• Good oral and written communication skills.

Experience

Candidates should have 3-5 years of hands-on experience in analytical method development and validation.

Good to Have

• Hands-on experience on Mass Hunter Software.

Benefits

• Generous annual leave.
• Reward plans.
• Flexible working schedules, dependent on role.
• Access to tailored health support.
• Meaningful ways to give back to the community.
• Access to Twist, Teva’s career development platform, including learning programs, short-term projects and opportunities for internal growth.

How to Apply

Interested candidates can apply online through the official Teva careers page using the link below.

Already working at Teva? Apply through the internal career site on Twist.