Associate Director, Global Quality Compliance & Computer Systems
Listed on 2026-01-25
-
IT/Tech
Data Analyst -
Quality Assurance - QA/QC
Data Analyst
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Associate Director, Global Quality Compliance & Computer SystemsDate:
Jan 20, 2026
Location:
Parsippany, United States, 07054
Job
Who we areWe’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You ll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.
The opportunityThis role will have oversight, accountability, and associated responsibilities for projects and enhancements, deployments, and ongoing operations for the Veeva Global GxP Quality Management / Electronic Document Management System (QMS/EDMS) Program and other assigned Global Quality Computer Systems as a PMO lead.
Location:
This is a hybrid role (3 days/week onsite) based in Parsippany, NJ.
* This is a temporary assignment planned to go through 2028
- Manage defined implementation project schedule and activities related to the Veeva Global GxP program, including oversight for global and site communication plan in alignment with Communication Lead, business prioritization of key activities, issue escalation, and risk mitigation. Partner with the appropriate functions (Business, IT) to provide issue resolution.
- Directing activities/priorities for external contractor(s) (e.g. Deployment Leads, Change Management and Training Lead) assigned to the Veeva Global GxP program.
- Support overall Teva Quality team with daily operational activities such as attending meetings/training sessions, etc.
- Developing and implementing guidance and templates to enhance business program management activities.
- Support business workstream activities for the Veeva project including, but not limited to:
- Participate in functional and process design review sessions as needed, assist Business Leads with documenting open questions, addressing follow-ups, etc.
- Provide support to project Subject Matter Experts (SMEs) as needed (e.g. during process review sessions, testing activities, etc.)
- Assist with creation/review of associated work instructions, procedures, training modules for business workstream
- Work closely with IT teams and support Business and IT Deployment Leads with deployment and migration related activities as needed
- Provide updates in program and Quality Global/regional/leadership meetings
- Serve as the backup to the Head of Global Quality Computer Systems as assigned
- Additional activities as assigned
Any equivalent combination of education, training and/or experience that fulfills the requirements of the position will be considered.
- Bachelors in Science is required and advanced degree preferred in science/regulatory/computer science/management field
- Minimum of 8 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
- Minimum 5 years experience as project/program management leading complex GxP projects including implementation/deployment and data migration in the pharmaceutical industry
- Demonstrates resourcefulness and initiative and creates an appropriate level of urgency to meet objectives and deadlines
- Experience working in large, multinational companies leading cross-functional teams
- Prior experience with Veeva Quality Vault is preferred
- Proficiency in MS Office tools including MSProject
The annual starting salary for this position is between $154,000 - $202,125 annually. Factors which may affect starting salary within this range and level of role may include geography/market, skills, education, experience and other qualifications of the successful candidate.
How We ll Take Care of YouWe offer a competitive benefits package, including:
- Com…
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