Key Responsibilities

- Implement and uphold cGMP-compliant facility management and administrative processes.
- Handle USFDA and other regulatory audits, from coordination to ensuring zero deviation execution.
- Provide daily oversight of security services, pantry/canteen, and cleaning operations.
- Drive 100% compliance with SOPs and ensure that practice aligns with documented procedures.
- Monitor Quality Management System (QMS) activities daily and support seamless internal and external audits.
- Generate and manage Management Information System (MIS) reports, dashboards, and audit trackers.
- Ensure training and performance reviews for all support and outsourced staff.
- Supervise vendor management, including bills, services, and budget control.




- Track and maintain consumables, materials, and vendor coordination logs.
- Drive continuous improvement in service quality and stakeholder satisfaction.

Desired Profile

- Solid background in administration within pharma manufacturing units.
- Familiar with regulatory audit environments such as USFDA, WHO, etc.
- Good understanding of SOP implementation, QMS, and cGMP norms.
- Skilled in MIS/data reporting and vendor management.
- Excellent coordination, communication, and execution skills.

📌 Executive / Sr. Executive - Admin (Secunderabad)
🏢 Biological E
📍 Secunderabad