Sr Mgr Quality Assurance- On Site CMO Manager

About the role

The role provides end-to-end quality oversight, risk management, and QMS governance for external manufacturing operations, ensuring adherence to cGMP requirements, regulatory expectations, Teva quality standards, and Quality Technical Agreements while supporting uninterrupted product supply Pharmaceutical QMS (Deviations, CAPA, Change Control, Investigations, APR/PQR, Validation, SOPs).

What you'll do

• Be part of a high-performing, inclusive culture that values fresh thinking and collaboration
• Have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together
• Participate in daily production and operational review meetings to provide quality oversight and ensure alignment with production objectives
• Monitor adherence to cGMP requirements, approved procedures, and quality standards through routine shop floor engagement
• Provide real-time visibility and escalation of critical quality events, deviations, compliance concerns, and operational risks

What you need

• 12–22 yrs of experience
• GMP
• ISO 9001
• SOP writing
• Complaint handling
• Regulatory affairs
• Lean
• Any graduate

Good to have

• Chemistry