Aseptic Groninger Technician - Fill/Pack Equipment Specialist

Fagron; Wichita (KS); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

401(k) with company match

Medical, Vision and Dental insurance

Health Savings Account (HSA)

Paid time off

Job summary

Fagron in Wichita, KS, seeks a Groninger Technician to set up, operate, and troubleshoot automated filling, stoppering, capping and packaging equipment in a sterile, FDA-regulated 503B facility. The role ensures compliance with cGMP and quality standards.

You will support maintenance, validations, investigations, CAPAs, and continuous improvement while collaborating with Production, Quality, Validation and Engineering teams.

Qualifications

• Associate degree in a technical field preferred.
• 2–5 years of pharmaceutical manufacturing or maintenance experience.
• Experience with Groninger equipment strongly preferred.
• Experience in sterile, aseptic, or injectable manufacturing environments preferred.
• Knowledge of automated filling and packaging systems.
• Understanding of cGMP requirements and aseptic manufacturing.
• Ability to read schematics and technical documentation.
• Strong troubleshooting and root-cause analysis skills.
• Excellent communication and teamwork skills.

Responsibilities

• Operate and set up Groninger filling and packaging equipment.
• Perform changeovers, adjustments, and line clearances.
• Monitor equipment performance and troubleshoot issues.
• Perform preventive and corrective maintenance.
• Maintain GMP-compliant documentation and records.
• Support validations, investigations, CAPAs, and continuous improvement initiatives.
• Collaborate with Production, Quality, Validation, and Engineering teams.

Skills

Groninger equipment

cGMP knowledge

Troubleshooting

Root-cause analysis

Aseptic manufacturing

Reading schematics

Documentation

Communication

Teamwork

Pharma manufacturing experience

Education

Associate degree

Job description

Fagron in Wichita, KS, seeks a Groninger Technician to set up, operate, and troubleshoot automated filling, stoppering, capping and packaging equipment in a sterile, FDA-regulated 503B facility. The role ensures compliance with cGMP and quality standards.

You will support maintenance, validations, investigations, CAPAs, and continuous improvement while collaborating with Production, Quality, Validation and Engineering teams.