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!
Job Description
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. Also to help Registered Pharmacist in product disposition process.
- 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
- 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
- University degree from Pharmacy (Pharmacist)
- 1 - 2 years in Quality Assurance of multinational - pharmaceutical company. Fresh graduates are welcome to apply
- Proficient in English, at least in writing and reading
- Analytical Skills
- Computer Literacy & English Proficiency
Quality
Sub Function
Manufacturing Quality Assurance
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:
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