Associate Director IT Quality and Compliance – TAPI

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.

Location of the position

This position is available in Rho (IT), Amsterdam (NL) or near out production sites in Croatia, Hungary or Czechia.

The opportunity

The main purpose of your job will be to ensure that GxP Computerized Systems and infrastructure implementation and maintenance are managed according to TAPI policies, standards, and procedures. You will be the IT Business Partner on Computerized Systems Governance to all TAPI sites. Within this role, you shall maintain effective working relationships with peers within the TAPI Quality and TAPI IT organization. This position is accountable to ensure that the TAPI QMS related to GxP Computerized System is in constant alignment with current regulations, data integrity principles, industry guidance and inspection trends. 

How you’ll spend your day

• Continuously improve the TAPI cGxP Computerized Systems policies, standards, procedures, tools and training.
• Provide QA IT review and approval on all globally managed Computerized System deliverables
• For some globally managed Computerized System, represent site users, as System Business owner. Manage site inspection readiness and support with regards to globally managed Computerized Systems.
• Guide TAPI Sites IT and IT QA on inspections trends, observations, authorities’ expectations and best practices that can mitigate gaps.
• Deliver training programs to TAPI Computerised systems owners.
• Support sites with any IT related project(s) as required.
• Support sites with computer systems validation, infrastructure qualification and systems life cycle management, together with any remediation needed.
• Conduct GxP computerized systems gap assessments/evaluations with applicable regulations

Your experience, skills and qualifications

• Bachelor’s degree in Engineering, Computer Science, Science or other related field.
• Minimum of 10 years of experience and strong overall understanding of Computerized System Validation and quality business processes supporting global functions, manufacturing and laboratory operations
• Working experience in API/Pharma companies in a similar role is a must.
• Proven management capabilities managing direct and matrix teams and projects
• Strong understanding of regulations and industry standards such as 21 CFR Part-11, Eudralex Annex-11, GAMP 5, Data Integrity regulatory and industry Guidance and proven ability to pragmatically apply these regulations to operate in an efficient and effective fashion.
• Exposure, working experience and knowledge of GAMP -5 and SCADA systems
• Ability to work with external vendors/suppliers, experience with IT supplier management is desirable.
• Advanced leadership skills, business strategy, accountability, proven experience leading and motivating global, cross-functional teams.
• International experience – a must.
• Advanced experience in working with matrix environment.
• Advanced negotiation skills.
• Advanced knowledge and experience in problem solving.
• Advanced communication skills – written and verbal.
• Advanced agility leadership and teamwork skills.
• Must be able to travel based on business need; up to 30% when critically required (domestic and international).
• Fluent in English – a must

Pre Employment Screening

TAPI will carry out appropriate verification and legally permitted vetting prior to the confirmation of any offer of employment. More information on this verification and vetting will be provided if you reach this stage of the application process.

Reports To

Director IT Quality & Compliance

Contact person

Vincent van Straten – Team Lead Recruitment

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. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

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