Reviewer Production Documentation

at  Teva Pharmaceuticals

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Reviewer Production Documentation
Date: Aug 30, 2024
Location:Haarlem, Netherlands, 2031
Company: Teva Pharmaceuticals
Job Id: 57920

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

We are looking for a meticulous Reviewer Production Documentation to join our team. In this role, you will ensure the accuracy, completeness, and compliance of all documentation throughout the drug manufacturing process. Stationed in the production department, you will work closely with operators and collaborate with various departments, including Parenterals, Quality Assurance, and Packaging. Your responsibilities will include guiding operators in proper documentation practices according to ALCOA++ principles, compiling and organizing relevant documents, reviewing BMRs/CVPs for completeness, and driving continuous improvements in the documentation process. This role is essential in maintaining the highest standards of compliance and quality in our production operations.

YOUR EXPERIENCE AND QUALIFICATIONS

• Knowledge of GMP guidelines and ALCOA principles.
• Experience with quality management systems like Trackwise.
• Familiarity with BMR/CVP processes in pharmaceutical manufacturing.
• 2-4 years of experience as an operator or documentation specialist in a pharmaceutical setting preferred.
• Experience with MES and SAP is a plus.

Please refer the Job description for details