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

The IT business process analyst will be responsible for the support and maintenence of teva global serialization systems (SAP ATTP & Tracelink). In this role the individual will be responsible for ensuring initiatives and projects meet the core business requirements and impacted business processes are updated. These global business processes are applicable to both internal sites and business functions and external secondary packaging CMOs & 3PLs.

How you\'ll spend your day

• Manage assigned global cross-functional strategies and activities associated with the implementation and management of serialization activities for all commercial products across all manufacturing sites including all contract manufacturing organizations (CMOs).
• Reviews and provides feedback on serialization and traceability requirements in quality agreements.
• Responsible for completion of business process change impact assessments for sustainment initiatives
• Manage the completion of business process and system regression testing as required by Teva\'s IT validation processes
• Develops, implements and maintains oversight on policies and procedures for the operation of the Global Serialization activities, ensuring all relevant business and regulatory requirements are met.
• Works on problems of moderate to advanced complexity where analysis of situations or data requires an evaluation of intangible variables.
• Reviews, and/or implements changes to controlled documents as needed.

Your experience and qualifications

• Experience working with change controls and GxP validation protocols.
• Exceptional verbal and written communication skills.
• Good organizational and time management skills.
• In-depth understanding and application of relevant principles, concepts, practices, and standards, along with an in-depth knowledge of industry practices and regulations.
• Solid working knowledge and expertise of relevant US, EU and international pharmaceutical cGMPs / regulations
• Ability to collaborate cross-functionally
• 2+ Years of experience as functional consultant on Enterprise Serialization Platform - SAP ATTP, TraceLink.
• English - Proficient level

Reports To

Director IT Business Application

Already Working @TEVA?

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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.

Teva Pharmaceuticals