Job Description

Who are we?

Teva is a global pharmaceutical leader and the world\'s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world\'s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we\'ve built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

• Good experience in handling Granulation, Compression, Encapsulation & Coating process and equipment.
• Knowledge on Regulatory requirements of different markets like, Japan, Europe, Canada, US and rest of world (ROW) markets.
• Preparation & execution of Transfer strategies for scale up batches, transfer batches with proper documentation for new launch / validation batches
• Responsible for New product, Site transfer, Troubleshooting, execution of the product robustness program and Market support program on the shop floor.
• Risk assessment of process parameters and material attributes with combination of prior knowledge of experiments to establish a design space or other representation of process understanding.
• Identify the critical process parameters and input material attributes that must be controlled to achieve quality attributes of the final product.
• Utilization of Knowledge of unit operations, analytical and statistics for process validation activity.

Contd...

• Documentation such as preparation and review of Batch records, Protocols, Reports, etc. required for execution
• To support and coordinate cross functional teams i.e. with QA, QC, Production, warehouse & Purchase department for completion of projects in a cost effective manner
• To support the Regulatory Affairs department for submission.
• Follow up for licensing information for manufacture of drug product, import of drug substance and drug product related to site transfer projects
• To complies with GMP and safety procedures in working area
• Handling of Trackwise, Glorya & SAP
• Experience of handling of change control, Investigation, CAPA, Deviations and OOS

Qualifications

• Experience in MS&T (Technology Transfer) about 5-8 years.
• Educational requirement - Master of pharmacy/Bachelor of pharmacy.

Function

Manufacturing

Sub Function

Technical Transfer

Reports To

In process of validation

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply:

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

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.

Teva Pharmaceuticals