Manufacturing Supervisor

Responsibilities

• Lead a team of operations personnel in the manufacturing of sterile injectable drug products
• Ensure compliance with current Good Manufacturing Practices (cGMP) and EHS regulations
• Supervise day-to-day production, scheduling, staffing, and material management
• Review and manage documentation for batch and system records
• Implement training programs and performance measurement systems
• Lead technical reviews, investigations, and process improvement projects using Root Cause Analysis (RCA)
• Represent the company during audits and inspections

Requirements

• High School diploma or GED required
• Minimum 2 years of manufacturing or operations support experience
• Minimum 1 year of leadership experience
• Proficiency in Microsoft Office (Word, Excel, Outlook)
• Ability to lift up to 50 pounds and perform physical tasks in a clean room environment
• Ability to gown qualify for Grade A/B areas

Preferred Qualifications

• Bachelor's Degree in a science, engineering, or business discipline
• Experience with enterprise software such as Microsoft Dynamics, Veeva, PowerBI, or Trackwise

About the Company

Simtra BioPharma Solutions is a world-class Contract Development Manufacturing Organization (CDMO) that partners with pharmaceutical and biotech companies to bring sterile injectable products to market, including biologics, small molecules, and vaccines.