Quality Analyst III

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.

The opportunity

To manage the EMSO Quality system requirements in accordance with Teva quality standards and in compliance with the regulatory requirements.

This activity has the following aspects –

• Responsible to follow the Quality Management System of EMSO organization, which is relevant to job function.
• Quality Management System – Change control, Deviation and complaints.

KPI Metrics and improvement actions for QMS system.

How you’ll spend your day

• Quality System Management for EMSO: Ensure Quality management system is in place for EMSO APAC through implementation and maintenance of SOPs related to the various job functions and compliance to the SOPs
• Review of Change controls/Batch Records/Investigations: Ensure change controls are reviewed as per regulatory requirements in timely manner. Review of batch manufacturing and packing records along with associated validations and periodic batch record reviews. Review of investigations pertaining to deviations and complaints as per requirements.
• CFT Co-ordination: Co-ordinate internally within EMSO and with other regions to meet the business requirements and escalations, if any
• KPI Metrics: Ensure KPI Metrics met the requirements for EMSO Quality and ensure no overdue QMS elements.
• Any other duties as assigned by the supervisor

Your experience and qualifications

• M. Pharm / M.Sc. (Science).
• Minimum 10-12 years of experience in pharmaceutical industry.
• Experience of handling Operational Quality exposure
• Knowledge of cGMP, Quality management Systems and the pharmaceutical manufacturing, supply chain environment.
• Knowledge on Compliance Standards and Regulations as applicable to the market.
• Knowledge on Manufacturing process

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, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.