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
- Strong background in administration within pharma manufacturing units .
- Familiar with regulatory audit environments such as USFDA, WHO, etc.
- Positive 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