Mgr Quality Control

Mgr Quality Control

Date: May 27, 2024

Location:
Goa, India, 403722

Company: Teva Pharmaceuticals

Job Id: 48851

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

How you’ll spend your day
• To ensure planning and supervision of daily analysis activities in the commercial section.
• To ensure good laboratory practices and good documentation practices, to maintain RFT documentation.
• To ensure timely completion and submission of analytical reports to Quality Assurance within target Cycle Time (CT) with proper closeout of all relevant quality documents
• Responsible for Investigations of Deviations, OOS, OOT, Action Limit and Aberrant Analytical Test results, Chromatographic errors, Change Control and temporary changes
• To ensure that corrective and preventive actions are implemented and are effective
• To ensure the analysis of samples received against Product Deviations, MS&T Study Protocols, investigation and product complaint are completed as per the timelines
• Ensures review and locking of analytical results in SAP System and responsible for other SAP related activities
• To ensure maintenance and upkeep of logbooks, Inspection lot number register and all relevant registers in the laboratories
• Evaluation and approval of Annual Product Review report
• Ensure preparation, validation and verification of excel calculation sheets
• To monitor and maintain Action and Alert limits for all products at product anniversary date yearly
• Responsible for management of resources in Commercial section required for effective and efficient functioning of the laboratory investigation and revision of relevant SOP/STP
• Evaluation and approval and the change controls initiated in the Quality Control Department and evaluation of intradepartmental change controls
• Oversees the implementation of Standard Operating Procedures relating to the laboratory activities and compliance with the requirements of Good Manufacturing Practice (cGMP)

How you’ll spend your day
• Responsible for Approval of Specifications, Test Methods, Analytical Worksheet, Analytical Method Transfer/Verification/validation Protocol and Reports and Standard Operating Procedure of the Quality Control department.
• Ensures review and approval of departmental and site documents.
• Ensures Audit readiness of Quality Control Laboratory and to face all regulatory and customer inspections and ensure compliance.
• Identification, preparation and execution of cost improvement plans in co-ordination with OpEx team to reduce laboratory expenses.

Your experience and qualifications
• Bsc/Msc (Chemistry) with minimum 12 years of experience

Reports To

In process of validation

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Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, ****** orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws