Teva Jobs

Job Information

Teva Pharmaceuticals Quality Assurance Production Support Specialist in Zejtun, Malta

Quality Assurance Production Support Specialist

Date: Oct 15, 2020

Location: Zejtun, MT, ZTN 3000

Company: Teva Pharmaceuticals

Company Info

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!

The Position

Working within a challenging and exciting manufacturing environment and reporting to the Mgr Quality Assurance the selected candidate will be responsible for all functions as regards the issuing, reviewing and approval of production documents. We are looking for people who have a very good eye for detail and are precise in their work so as to ensure that such production documents are correctly filled and according to Company procedures. The QAPS Specialist will also be performing and approving amendments to production document templates as well as compiling of Product Quality Reviews. Since it’s a continuous changing working environment you will also be participating in ongoing continuous improvement projects within the department. This position is on a full-time indefinite basis and is based in Bulebel site .

The Applicant

We would like to hear from people who:

•Have an Ordinary Level standard of Education (Advanced Level of Education will be considered an asset) or at least have 5 years’ experience within the manufacturing of solid dosage pharmaceuticals

•Are proficient in Microsoft Office applications

•Fluent in both oral and written English

•Have excellent interpersonal and organizational skills with the ability to be assertive.

This position requires the individual to be able to work on a 2-shift basis

Function

Quality

Sub Function

Manufacturing Quality Assurance

Reports To

Mgr Quality Assurance

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.

EOE including disability/veteran

DirectEmployers