Job Title: Quality Control Technician II
Location: Gwalior, India, 477117
Company: Teva Pharmaceuticals
Who We Are
Teva Active Pharmaceutical Ingredients (TAPI) is a global leader in supplying high-quality APIs (Active Pharmaceutical Ingredients). With a broad portfolio of over 350 products, we support 80% of the top 50 pharmaceutical companies globally. Backed by more than 80 years of experience, TAPI is recognized as one of the most trusted suppliers in the industry. With a commitment to innovation and customer service, we operate across various global sites, providing high-quality APIs and ensuring industry-leading standards.
Key Responsibilities
Audit Readiness & Compliance:
Ensure 24x7 audit readiness and participate in internal, external, and regulatory audits.
Maintain compliance with cGMP (current Good Manufacturing Practice), GLP (Good Laboratory Practice), and safety guidelines in the laboratory.
Investigations & Reporting:
Initiate and investigate Laboratory Incident Reports (LIR), Out of Specification (OOS), Out of Trend (OOT), and borderline results, reporting them to the in-charge.
Support CAPA (Corrective and Preventive Action) training to ensure full participation.
Sampling & Analysis:
Sample and analyze raw materials (RM), finished goods (FG), intermediates, and cleaning samples as per requirements.
Enter results in analytical sheets, QA forms, LIMS (Laboratory Information Management System), and ensure data integrity.
Laboratory Equipment & Documentation:
Perform routine analytical tests as per standard operating procedures (SOP) and monographs.
Ensure calibration and verification of instruments and maintain stock records for chemicals and reconciliation of standards.
Maintain reserved samples room, chambers, autoclaves, and incubators.
Documentation & Support:
Help prepare and update department-related documents like SOPs and STPs (Standard Test Procedures).
Ensure timely sampling of finished products, raw materials, and intermediates, and send samples to external laboratories for analysis.
Team Coordination:
Determine team priorities in line with plant needs and coordinate with team leaders and managers.
Adhere to safety guidelines and ensure housekeeping standards are followed in the laboratory.
Qualifications and Experience
Educational Requirements:
Bachelor’s or Master’s degree in Science, preferably in Chemistry.
Experience:
Minimum of 3 years of experience in a Quality Control laboratory setting, preferably with wet chemistry experience.
Skills & Knowledge:
Strong understanding of laboratory practices, testing, and analysis.
Familiarity with cGMP, GLP, and safety regulations.
Ability to maintain detailed records and perform audits.
Teva’s Equal Employment Opportunity Commitment
Teva Pharmaceuticals is committed to providing equal employment opportunities for all individuals regardless of race, age, gender, disability, or any other legally protected status. We foster an inclusive work environment and are dedicated to supporting employees with any accommodations needed during the recruitment process.
If you are an experienced Quality Control Technician looking to contribute to a leading global company in the pharmaceutical industry, we encourage you to apply.
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