QC Technician Job Role at Teva Pharmaceuticals | Pharma Candidates Apply Now
Teva Active Pharmaceutical Ingredients (TAPI), a global leader in API manufacturing, is seeking to hire a Quality Control Technician III at its Gajraula facility in India. This role offers the opportunity to contribute to stability testing, GMP/GLP compliance, and analytical validations in a world-class pharmaceutical environment. Science and Pharmacy graduates with at least one year of experience are encouraged to apply.
Quality Control Technician III – TAPI
Date: Jul 4, 2025
Location: Gajraula, India, 244235
Company: Teva Pharmaceuticals
Job ID: 62461
Who we are
TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry’s broadest portfolio, including over 350 API products. We are the go-to global supplier of APIs, supporting 80% of the world’s top 50 pharmaceutical companies. We are proud of our reliable history in the generic API industry, dating back over 80 years, and our reputation as one of the most trusted API suppliers. These enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service.
Our employees are at the core of our success. Our headquarters are in Israel, and TAPI employs more than 4,000 professionals
at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling the timely introduction of new products to the market.Job Description:
- Analysis of stability samples & working standard qualification activity as per defined procedure & monograph.
- Maintaining a set of procedures supporting the ATS department for the implementation of GMP & GLP techniques.
- Maintaining a system of methods and specifications for all materials and products.
- Data filling and maintaining the log books, certificates, stability report, and stability data in the archive.
- Monitoring of stability studies per ICH Q1 and conducting analytical method validation activities per ICH Q2.
- To initiate the LIR / OOS if any procedural gap related to SOP/monograph is identified during routine activity.
- Qualifications of all analytical instruments should be maintained in the stability Section.
- Follow the established safety procedures during day-to-day laboratory activities.
- Any other job assigned by the Manager of Quality Control.
Your experience and qualifications:
- Bachelor’s/Master’s of Science/ B. Pharmacy
- One Years Experience
Keywords: Quality Control, QC Technician Job Role at Teva, Technician, TAPI, Job Posting, Teva Pharmaceuticals, Gajraula, India
