QA Specialist

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 someone :

• To help coordinate GMP aspects in manufacturing area according to European and local GMP regulation, EHS policy and Corporate policy that all activities in accordance with cGMP, EHS policy and Corporate policy
• To help Registered Pharmacist in product disposition process

How you’ll spend your day

• Review accurately product data which will be released or rejected based on their specification to certify product that will be released accurate according to specified quality and marketing authorization
• Coordinate execution of product document review according to the priority
• Ensure the completion of product documents for disposition process
• Ensure the archiving of product documentation
• Upload product documentation into the SharePoint
• Perform investigation and risk assessment as required
• Review the implementation of GMP aspects in the shop floor
• Responsible for checking all retained samples based on procedure
• Review the MPPCR and any other related documents prior to use for manufacturing and packaging process

Other tasks:

• Prepare and maintain product documents particularly and other documents generally which deal with team responsibilities according to cGMP, EHS policy and Corporate policy
• Ensure that medicinal products are distributed in accordance with GDP standard
• Implement cGMP, GDP and QEHS policy in the working area
• Consider cost effectively in all department activities so it will not exceed the specified budget

Your experience and qualifications

• Graduated Apothecary Program, from reputable University preferably
• Fresh graduates are welcome to apply
• Familiar with cGMP  
• Used to prepare report, has good communication and presentation skills
• Computer literacy and English proficiency

Make a difference with Teva Pharmaceuticals

Please submit your CV and a Cover Letter.
Please note that only shortlisted candidates will be contacted.

Reports To

QA Manager

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: Internal Career Site
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.