Quality Qualified Person

51109- Quality Qualified Person

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

• Contact person for the Israel Health and Regulatory Authorities
• Accompanies Israeli Ministry of Health regulatory inspections and responsible for providing inspectors with all relevant data
• Oversees the implementation of follow up and corrective actions committed to as a result of these external audits and the evaluation of effectiveness of corrections
• Oversees the product batch release process
• Oversees the implementation of Standard Operating Procedures relating to the release of products and compliance with the requirements of Good Manufacturing Practice (cGMP)
• Where deviations occur relating to the release process, ensures that they are fully documented and investigated, reported to Quality Assurance in a timely manner, as well as suggesting corrective action and preventive actions for future, where appropriate
• Stands as contact person for customers (within and outside Teva) for batch release purposes
• Ensure that testing and release or rejection of packaging materials and raw materials is performed according to approved standard operating procedures and test methods
• Evaluation of batch release after temperature excursion during shipment
• Ensures the documentation (batch files) is handled according to the relevant approved procedures
• Responsible for pre and post-printed approval of new editions of printed packaged materials
• Responsible for controlled drugs, including ordering, using for production and reporting to the Israeli Ministry of Health
• Responsible for authorization importation of materials
• Responsible for Pharmacist permit for costumer complaint samples & lab analysis materials import - Mslul
• Manages and executes the regulations of the Israeli Ministry of Health with regards to first batches for the Israeli market

We at Teva believe in equal employment opportunity, needed adjustments and adaptions to the work environment will be considered

Your experience and qualifications

• Graduate in Pharmacy, License to practice Pharmacy
• Intensive training in cGMP
• Experience in pharmaceutical manufacturing
• Certified Pharmacist for at least three years and has met all requirements of a Responsible Pharmacists , approved by the Israeli Ministry of Health