The opportunity
Are you ready to lead a high-impact team where quality, compliance, and documentation come together to uphold the integrity of pharmaceutical manufacturing? As Manager Quality Compliance & Documentation, you’ll play a critical role in shaping and safeguarding the quality standards at our site. This is your opportunity to influence how we manage regulatory compliance, ensure audit readiness, and drive continuous improvement, all while mentoring a capable team and working alongside cross-functional partners in a highly regulated environment.
You'll be part of a global organization that values operational excellence, collaboration, and proactive problem-solving and you'll help us deliver medicines that make a real difference in patients’ lives.
How you’ll spend your day
Lead & coach a team of 8–10 professionals, divided between Compliance and Documentation.
Own and continuously improve compliance processes, including:
Supplier qualification and Quality Technical Agreement (QTA) coordination
Inspection readiness, audit execution, and self-inspection programs
Handling vendor change notifications, data integrity initiatives, and Global Notification To Management (GNTM)
Managing corporate gap assessments and supporting CAPA implementation
Oversee documentation systems, ensuring:
Controlled issuance of SOPs, logbooks, and production batch records
Effective use and governance of the Electronic Document Management System (EDMS)
High-quality, audit-ready documentation across teams
Prepare for and lead third-party audits and act as a strategic support during government inspections, either in the front office or as back-office lead, depending on the situation.
Monitor and report on quality KPIs relevant to your area, translating performance insights into improvement initiatives.
Foster collaboration with cross-functional stakeholders and contribute to global knowledge-sharing across the Teva Quality network.
