Job Description

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

Education Required:
Bachelor\'s Degree preferably in Computer Science, Life Sciences, Information Systems Management, Computer Engineering, Electrical Engineering, or a related field or equivalent combination of relevant education and experience.
Experience Required:

• 4+ years working as a validation analyst / Data Integrity remediation activities
• 4+ years working in regulated pharmaceutical companies
• Experience in 21 CFR Part 11, GAMP
• Experience in SDLC (Agile or Waterfall)

Experience Preferred:

• 5+ years working as a validation analyst / Data Integrity remediation activities
• 5+ years working in regulated (GLP, GCP or GMP) biotech or pharmaceutical companies
• Experience in 21 CFR Part 11, GAMP
• Experience in SDLC (Agile or Waterfall)

Company/Industry Related Knowledge:
Experience working in a highly regulated environment within the Pharmaceutical Industry.
Knowledge and experience of cGMP and its implementation to laboratory instrumentation and laboratory processes.

How you\'ll spend your day

Bachelor\'s Degree preferably in Computer Science, Life Sciences, Information Systems Management, Computer Engineering, Electrical Engineering, or a related field or equivalent combination of relevant education and experience.

• 4+ years working as a validation analyst / Data Integrity remediation activities
• 4+ years working in regulated pharmaceutical companies
• Experience in 21 CFR Part 11, GAMP
• Experience in SDLC (Agile or Waterfall
• 5+ years working as a validation analyst / Data Integrity remediation activities
• 5+ years working in regulated (GLP, GCP or GMP) biotech or pharmaceutical companies
• Experience in 21 CFR Part 11, GAMP
• Experience in SDLC (Agile or Waterfall)

Experience working in a highly regulated environment within the Pharmaceutical Industry.
Knowledge and experience of cGMP and its implementation to laboratory instrumentation and laboratory processes

Your experience and qualifications

Bachelor\'s Degree preferably in Computer Science, Life Sciences, Information Systems Management, Computer Engineering, Electrical Engineering, or a related field or equivalent combination of relevant education and experience.

• 4+ years working as a validation analyst / Data Integrity remediation activities
• 4+ years working in regulated pharmaceutical companies
• Experience in 21 CFR Part 11, GAMP
• Experience in SDLC (Agile or Waterfall
• 5+ years working as a validation analyst / Data Integrity remediation activities
• 5+ years working in regulated (GLP, GCP or GMP) biotech or pharmaceutical companies
• Experience in 21 CFR Part 11, GAMP
• Experience in SDLC (Agile or Waterfall)

Experience working in a highly regulated environment within the Pharmaceutical Industry.
Knowledge and experience of cGMP and its implementation to laboratory instrumentation and laboratory processes

Reports To Assoc Dir R&D IT Lab and Global Systems Validation

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:

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