Quality Analyst I

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.

How you’ll spend your day

• Serve as an initial point of contact for Veeva Global GxP business questions related to QMS and EDMS processes.
• Act as a primary business liaison with the IT support (FAS) team for operational support activities.
• Lead updates to system-specific SOPs, WIs, CBTs as driven by business needs.
• Review and approve master data requests.
• Enhancement/change reviews: 
• Triage and initial review of system standard releases and new feature requests and business enhancement requests for feasibility with IT.
• Participate in system change request/release review and prioritization meetings (Change Advisory Boards) with counterparts in Information Technology (IT), Compliance, sites, and other internal Teva functions, and work with global teams to manage these requests towards features or usable workarounds.  
• Support Global Business Owners during enhancement and change request reviews with the Business globally, including managing global business reviews of enhancement requests and compiling business feedback as part of enhancement planning.  
• Ensure ongoing operational activities for the Veeva Global GxP system are aligned with global processes and standards.
• Conduct additional business training as needed post go-live to help adoption at sites.
• Partner with the appropriate functions (Business, IT) to provide issue resolution.
• Escalate issues to management as needed.
• Participate in system periodic and user access reviews.
• As needed, act as a Global Business Owner for system validation activities for operational changes (review/approval of system requirements and other validation documentation, approval/execution of system testing, etc.).  
• Provide updates in Quality Global/regional/leadership meetings as needed

Your experience and qualifications

• Bachelors in Science is required and advanced degree preferred in science/regulatory/computer science/management field 
• Minimum of 7-9 years in pharmaceutical or related industry is required
• In-depth knowledge of pharmaceutical quality and quality systems, with broad experience and exposure to best practices
• Knowledge of cGxP requirements, Quality related IT applications, and computer system validation and deployment
• Demonstrated experience with managing complex activities
• Must have international experience and experience working with large cross-functional teams 
• Technical knowledge and expertise with Quality Management computer systems including Electronic Document Management Systems (EDMS)and Quality Management Systems (QMS) and processes (such as deviations, CAPA, laboratory investigations, complaints, trends, change control, document management, notification to health authorities, notification to Management, etc.).
• Skilled with Excel, Word, PowerPoint, MS Project and SharePoint
• Demonstrates resourcefulness and initiative and creates an appropriate level of urgency to meet objectives and deadlines
• Fluent in English
• Verbal and written communication excellence required
• Veeva Quality system knowledge a plus
   

Reports To

Group Leader, 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. 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.