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Quality Analyst

Date: Feb 22, 2021

Location: Brno, CZ, 627 00

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. Our dedication to quality is everything we do is uncompromising, and covers every stage of the development, production and marketing of our medicines: from the supply of materials through manufacturing and approval by the strictest authorities in the world. Join us on our journey of growth! If you have previous experience in a QA position or Qualified Person within the Pharmaceutical Industry then we would love to hear from you!

Job Description

• Responsible for quality oversight and observance of Good Distribution Practice rules of the products marketed in the Czech Republic and in compliance with Act No. 378/2007 Coll., on Pharmaceuticals, as amended, relevant Decrees and/ or EU requirements

• Acts as Responsible Person for distribution according to Act No. 378/2007 Coll. on Pharmaceuticals, as amended

• As deputy of Responsible Person for narcotics according to Act No. 167/1998 Coll. on Narcotics, as amended

• Roll out of Teva Quality Management System at commercial units level (including local warehouses)

• Control observance of GDP requirements and assure compliance of the company with relevant local and EU legislation

• Manage GDP training at a local and EU level where relevant

• Attend to monthly EU quality councils

• Prepare data for monthly quality metrics

• Ensure the market release of the Teva products to the distribution from approved suppliers based on batch release documentation and transport conditions documentation

Qualifications

 

• Master´s Degree in Pharmaceutical Sciences, Chemistry or relevant science

• Approx. 2 years of experiences as a Qualified Person in a pharmaceutical company or importer/distributor company

• Demonstrated knowledge and working experience with GMP, GDP and government regulations for the Czech Rep.

• In-depth knowledge within pharmaceutical industry related to Quality Compliance

• Working knowledge of pharmaceutical import and distribution operations

• Ability to clearly communicate with all levels in the organization (stakeholders), as well as with Health Authorities

• Fluent knowledge of English language and Czech language

• Ability to work under pressure

• Open-minded personality, Continuous learner

• Proficient computer skills – MS Office (Word, Excel, PowerPoint), SAP/TrackWise is advantage

• Driving license – B, willingness to travel to our warehouse in Brno (in case you are from Prague/other location)

Function

Quality

Sub Function

Commercial Quality

Reports To

In process of validation

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.