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

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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.