We re seeking a detail-oriented and technically skilled qualified to take on the role of QC Technician at our cutting-edge manufacturing facility. This role is critical to ensuring the integrity, compliance, and reliability of our stability testing and analytical operations.

Key Responsibilities:

1. Analysis of stability samples, Finish Product samples & working standard qualification activity as per the defined procedure & monograph.
2. Deep knowledge about the HPLC, GC, KF, Auto titrator, Vacuum open operation procedure as well as troubleshooting by following the GLP practices.
3. Maintaining a system of methods and specification for all materials and products.
4. Data filling and maintaining the logbooks, certificate, stability report and stability data in archive.
5. To initiate the LIR / OOS if any procedural gap related with SOP / monograph during routine activity.
6.



Qualifications of all analytical instruments should be maintained in stability Section.
7. Follow the defined safety procedure during day-to-day activity in laboratory.

Minimum Required Skills:

- Solid understanding of Quality Control procedures.
- Strong knowledge of GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices).
- Ability to handle instrument troubleshooting and follow documentation protocols. Qualifications

The candidate must have: Experience Level: 3-6 Years

Industry Experience: API/Pharma Experience is required

Qualification: M.Sc. in Chemistry

Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

📌 Quality Control Technician (HPLC) (Bijnor)
🏢 Teva Active Pharmaceutical Ingredient
📍 Bijnor