QC Job at Teva Pharma! BSc & MSc Chemistry Apply Online
Quality Control Technician III – TAPI
Date: Dec 23, 2024
Location: Gwalior, India, 477117
Company: Teva Pharmaceuticals
Job Id: 59906
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 for APIs, supporting 80% of the top 50 global pharmaceutical companies.
We are proud of our reliable history in the generic API industry dating back over 80 years and the fact that we are considered one of the most trusted API suppliers. This reputation enables TAPI to lead the industry based on our experience, expertise, technologies, and exceptional customer service.
Our employees are at the core of our success. Headquartered in Israel, TAPI employs more than 4,000 professionals across 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 timely introduction of new products to the market.
How you’ll spend your day
- 24 × 7 audit readiness.
- Experience on HPLC and Empower software.
- Basic Chemistry Knowledge.
- Responsible to work in different shifts.
- Participation in internal, external, and regulatory audits.
- Ensure 100% participation in training related to CAPAs.
- Responsible for initiating and investigating LIR, OOS, OOT, and borderline results and reporting them to the in-charge.
- Supporting document sharing from QC to RA/other requirements.
- Determining team priorities in accordance with the plant’s needs, while coordinating with the team leader/Manager.
- Following housekeeping, cGMP, GLP, and Safety Guidelines in the laboratory.
- Sampling and analysis of RM/FG/intermediates/cleaning samples based on requirements and result entry in analytical sheets, QA forms, LIMS, and online documentation as per data integrity norms.
- Performing analytical tests according to the monograph and SOP.
- Responsible for calibration and verification of instruments.
- Maintaining reserved sample rooms, chambers, autoclaves, and incubators.
- Assisting in-charge with document preparation related to the department (e.g., STPs, SOPs).
- Ensuring the sampling of finished products, raw materials, and intermediates, and sending samples to outside laboratories for analysis.
- Ensuring sampled, approved, and rejected labels are prepared on time as required.
- Responsible for maintaining stock records of chemicals and reconciliation of standards.
- Performing any other job assigned by the QC Manager or Group Leader – QC.
Your experience and qualifications
- Bachelor/Master of Science (Chemistry).
- Minimum 3 years of experience.
Link to Original Notification to apply: APPLY ONLINE HERE
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