Lead Manufacturing Technician - Aseptic & Biopharma Ops

PCI TRGR Penn Pharmaceutical Services Ltd; Madison (WI); On-site; USD 75,000 - 95,000; Full time

Job summary

PCI Pharma Services in Madison, WI seeks a Manufacturing Technician IV - Lead to supervise complex biopharma manufacturing tasks in a GMP environment. You will prep equipment, dispensing, dissolution, aseptic filling, packaging, and mentor junior staff.

Lead daily tasks, manage schedules, ensure SOP/MBR compliance, and escalate issues to management. Requires 4+ years of cGMP pharma experience and strong aseptic techniques.

Qualifications

• Requires a high school diploma with 4+ years of cGMP Pharmaceutical experience to include finished dose form.
• Strong knowledge of aseptic techniques and fill finish experience required.
• Experience in reviewing and creating controlled documents.
• Detail oriented with strong mechanical aptitude.
• Positive attitude and strong interpersonal skills to resolve and de-escalate issues.

Responsibilities

• Maintains and adheres to safe work habits and all applicable PCI safety procedures and guidelines.
• Leads team to accomplish daily tasks
• Maintains weekly/daily schedule up to date and provides direction to team
• Accountable for completing daily tasks and reporting issues to management
• Trains and guides less experienced personnel
• Prepares equipment and components for sterilization and Lyophilization
• Operates processing equipment including autoclaves, ovens, vial washers, and depyrogenation, centrifuges, mills equipment.
• Assists in the formulation and dispensing of product in a clean room environment per SOPs and MBRs
• Trous in and resolves problems with equipment or processes in the course of performing job duties

Skills

Aseptic techniques

Leadership

Troubleshooting equipment

Documentation

Safety compliance

Education

High school diploma

Tools

MS Office

Job description

PCI Pharma Services in Madison, WI seeks a Manufacturing Technician IV - Lead to supervise complex biopharma manufacturing tasks in a GMP environment. You will prep equipment, dispensing, dissolution, aseptic filling, packaging, and mentor junior staff.

Lead daily tasks, manage schedules, ensure SOP/MBR compliance, and escalate issues to management. Requires 4+ years of cGMP pharma experience and strong aseptic techniques.