Quality Control Technician III

Goa 3-5 year

Job Description

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

Our Team, Your Impact

Join our Nitrosamine team at the Watson Pharma Pvt. Ltd Goa Facility and contribute to ensuring the safety of pharmaceutical delivery systems. This role offers an exciting opportunity to work in a collaborative environment, supporting critical studies that impact patient safety and regulatory compliance. If you are detail-oriented, proactive, and passionate about analytical science, this position will allow you to develop your expertise and make a meaningful impact.

How You’ll Spend Your Day

Develop / Validate analytical methods for nitrosamines related activities using LCMS, GCMS, IC under guidance from senior team members.
Management of samples received from different sites for Nitrosamine project.
Testing of samples for nitrosamines related activities .
Trouble shooting of analytical instruments for difficulties faced during day-to-day operations.
Contribute in maintaining the prerequisites for Laboratory such as Column, Standards, Chemicals, Spares and Consumables etc.
Preparation of analytical protocols, reports, and technical documentation in compliance with regulatory standards.
Conduct routine instrument operation, calibration, and maintenance activities; escalate issues for troubleshooting.
Ensure accurate documentation of instrument usage, calibration records, and compliance.
Adhere to EHS guidelines and maintain safe laboratory practices.
Laboratory compliance and data integrity during day-to-day operations.
Participate in internal audits and contribute to readiness for external inspections.

Your Skills and Experience

Qualification: M.Sc. In Chemistry or M.Pharm
Experience: 3-5 years of hands on experience in analytical method development and validation.
Good Knowledge of Analytical Chemistry especially in Analytical method Development & Validation for Nitrosamine Impurities in Drug Substance and Drug Product and logical approach.
Literature Search for development of analytical methods.
Familiarity with computerized systems such as TrackWise, Veeva Vault
Experience in cGMP/GLP environments and regulatory-compliant documentation.
Strong attention to detail and ability to work effectively in a team setting.
Good communication skills (oral and written).
Sound knowledge of pharmaceutical Quality System, ICH guidelines etc.

Also Good to Have

Hands on experience on Mass Hunter Software.

How We’ll Take Care of You

At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community.  When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way. 

Already Working @Teva?

Make sure to apply through our internal career site on Twist—your one-stop shop for career development

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Quality Control Technician III

Job Description

Categories