Job Title: Quality Control Technician II
Location: Gwalior, India, 477117
Company: Teva Pharmaceuticals
Job ID: 57899
Who We Are
Teva Pharmaceuticals is on a mission to make healthcare more affordable and accessible for people around the world. As the leading manufacturer of generic medicines, we provide many essential products listed on the World Health Organization's Essential Medicines List. At least 200 million people globally take our medicines every day, and we continue to innovate to make a positive impact on health.
How You’ll Spend Your Day
Audit Readiness:
Ensure readiness for internal, external, and regulatory audits, maintaining compliance at all times.
Participate in audit activities and ensure all documentation is prepared for inspection.
Training:
Ensure 100% participation in training sessions related to Corrective and Preventive Actions (CAPAs).
Investigation of Results:
Initiate and investigate LIR (Laboratory Investigation Report), OOS (Out of Specification), OOT (Out of Trend), and borderline results, reporting findings to the in-charge.
Documentation Support:
Assist in sharing necessary documents from Quality Control (QC) to Regulatory Affairs (RA) or other departments as needed.
Team Coordination:
Determine priorities for the team based on plant requirements and coordinate with team leaders and managers to meet goals.
Compliance with Guidelines:
Ensure compliance with cGMP, GLP, and Safety Guidelines in the laboratory.
Sampling and Analysis:
Perform sampling and analysis of Raw Materials (RM), Finished Goods (FG), intermediates, and cleaning samples, ensuring results are documented properly in analytical sheets, QA forms, and LIMS. Follow data integrity norms for documentation.
Testing:
Conduct analytical tests according to monographs and Standard Operating Procedures (SOPs).
Calibration and Maintenance:
Ensure calibration and verification of laboratory instruments.
Maintain reserved sample rooms, chambers, autoclaves, and incubators.
Document Preparation:
Assist in the preparation of departmental documents such as STPs and SOPs.
Labeling and Stock Maintenance:
Ensure proper sampling, approval, and rejection of labels as required.
Maintain stock records of chemicals and reconcile standards.
Other Duties:
Assist the QC Manager or Group Leader with any additional tasks assigned related to quality control.
Your Experience and Qualifications
Educational Qualifications:
B.Sc. / M.Sc. in relevant scientific discipline.
Experience:
3-6 years of relevant experience in HPLC with Empower software.
Strong understanding of Quality Control (QC) processes, as well as GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices).
Shift Flexibility:
Ability to work in 24/7 shifts as required.
Teva’s Equal Employment Opportunity Commitment
Teva is committed to equal opportunity in employment, providing a work environment where all employees are treated with respect and dignity. We believe in diversity and inclusion, offering a fair and accessible recruitment process for all candidates.
If you have the required qualifications and are ready to take on this exciting opportunity to contribute to quality control at Teva, we would love to hear from you!
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