Manufacturing Setup Technician

Kindeva Drug Delivery; Lexington (KY); On-site; USD 50,000 - 75,000; Full time

Job summary

Kindeva Drug Delivery in Kentucky is seeking a Setup Technician, Manufacturing to support Filling, Assembly, and Packaging operations. You will set up equipment, verify performance, troubleshoot issues, and execute production with GMP compliance.

You will serve as an equipment SME, collaborating with Engineering and Maintenance, training team members, and driving continuous improvement in setup efficiency and process reliability.

Qualifications

• 2+ years of GMP manufacturing experience focusing on equipment setup, operation, and troubleshooting.
• Ability to make sound compliance decisions with moderate supervision.
• Strong knowledge of GMP, SOPs, and production processes in a regulated environment.
• Excellent communication, leadership, and organizational skills.

Responsibilities

• Lead and perform equipment setup, verification, clearance, and changeover activities for Filling, Assembly, and Packaging operations.
• Ensure equipment is properly set up, verified, and ready to support production execution.
• Perform work in accordance with established procedures and GMP requirements.
• Serve as an equipment SME and key point of contact for troubleshooting; adjust as needed to support performance.
• Train and develop team members; maintain up-to-date training records.

Skills

GMP experience

Equipment setup

Troubleshooting

Team collaboration

Education

High school diploma or equivalent

Job description

• (1)-1st shift (5:00 AM - 3:30 PM Monday-Thursday & every other Friday)


• (1)-2nd shift (3:00 PM - 1:30 AM Monday-Thursday & every other Friday)

Open Positions

• (1)-1st shift (5:00 AM - 3:30 PM Monday-Thursday & every other Friday)


• (1)-2nd shift (3:00 PM - 1:30 AM Monday-Thursday & every other Friday)

The Impact You Will Make

As a Setup Technician, Manufacturing, you will play a critical hands-on role in keeping our Filling, Assembly, and Packaging operations running safely, efficiently, and compliantly.

You will be responsible for equipment setup, operational verification, troubleshooting, production execution, clearance, and changeovers while ensuring adherence to established procedures and Good Manufacturing Practices (GMP).

You’ll also serve as an equipment Subject Matter Expert (SME), working closely with Manufacturing, Engineering, and Maintenance to troubleshoot equipment and process issues, support and train team members, and continuously improve equipment setup and performance.

What You Will Do

Equipment Setup, Changeovers & Production Readiness

• Lead and perform production room release, equipment setup, operational verification, clearance, and changeover activities for Filling, Assembly, and Packaging operations.


• Help ensure equipment is properly set up, verified, and ready to support production execution.


• Perform work in accordance with established procedures and GMP requirements.

Equipment Troubleshooting & Technical Support

• Serve as an equipment SME and key point of contact for equipment and process troubleshooting.


• Troubleshoot mechanical and operational equipment issues and make appropriate adjustments to support equipment performance.


• Partner with Engineering and Maintenance personnel to identify and resolve equipment and process issues.

Training & Team Development

• Help ensure team members are fully trained on equipment, processes, and GMP standards associated with the setup, operation, and maintenance of production equipment.


• Maintain up-to-date training records.


• Provide ongoing coaching and development to team members.

Continuous Improvement

• Identify opportunities to improve equipment performance, processes, efficiency, and throughput.


• Collaborate with cross-functional teams to implement Lean manufacturing initiatives and other continuous improvement strategies.

Shift & Team Coordination

• Coordinate with technicians, Manufacturing leadership, and support departments to ensure smooth transitions between production processes.


• Work collaboratively across functions to maximize efficiency and throughput while maintaining safety, quality, and compliance expectations.

Basic Qualifications

What You Will Bring

• High school diploma or equivalent.


• 2+ years of Good Manufacturing Practice (GMP) manufacturing experience with specific focus on equipment setup, operation, and troubleshooting.


• Ability to make sound decisions regarding compliance-related issues with moderate supervision.


• Strong knowledge of GMP, Standard Operating Procedures (SOPs), and production processes in a regulated environment.


• Excellent communication, leadership, and organizational skills.


• High level of personal and departmental accountability and responsibility.


• Ability to work effectively within a team environment to maximize efficiency and throughput.

Physical Requirements & Work Environment

• Regularly use hands to handle materials and supplies.


• Use computers for extended periods during the workday.


• Communicate effectively by telephone and electronic means.


• Regularly stand and walk for extended periods.


• Occasionally lift and/or move up to 25 pounds.


• Use proper lifting techniques and maintain awareness of workplace hazards.


• Have adequate vision to read and execute documentation and perform job responsibilities compliantly and safely.


• Follow all site safety procedures.


• Work in an environment that may include high-potency chemical compounds, hazardous materials, toxic substances, and controlled substances.


• Adhere to stringent Personal Protective Equipment (PPE) requirements and safe work methods and practices to ensure the safety and quality of personnel and finished product.

#WH

California residents should review our Notice for California Employees and Applicants before applying.

Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees—regardless of format—without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.

Equal Opportunity Employer

Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.