Pharmaceutical Development Technician I

About the Role

Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. This role supports the business needs of the organization while ensuring quality and compliance in all operations.

Position Summary

We have an opportunity for a Pharmaceutical Development Technician I to join our team. In this role, you will perform setup, teardown, manufacturing, and cleaning of equipment and processes under the guidance of senior technicians. You will follow policies and procedures with a strong focus on regulatory compliance, including SOPs, cGMP, and safety standards.

• Shift: M-F 2pm-10:30pm
• Location: Kansas City, MO
• 100% Onsite

Key Responsibilities

• Ensure cGMP compliance and maintain good housekeeping practices
• Follow all Catalent safety procedures and communicate necessary adjustments to address potential safety concerns
• Ensure proper use of Personal Protection Equipment (PPE)
• Learn all equipment and testing within the core group while maintaining high quality standards
• Maintain up-to-date training on equipment and site procedures
• Perform daily tasks to keep working areas stocked with proper materials and supplies
• Conduct physical characterization testing on raw and in-process materials
• Support sampling and packaging of in-process and finished product material
• Maintain active inventory of excipients and active pharmaceutical ingredients used for experimental processing
• Perform all other duties as assigned

Requirements & Tech Stack

• High School Diploma or General Educational Development
• 0+ years of relevant work experience
• Excellent written and verbal communication skills with internal and external customers, peers, and managers
• Well organized with the ability to multitask and work effectively under pressure to meet deadlines
• Individual may be required to sit, stand, walk regularly and occasionally lift up to 50 pounds

Preferred Skills & Background

• Demonstrated outstanding troubleshooting skills preferred
• Experience maintaining high quality laboratory documentation in accordance with applicable regulatory guidance and site Standard Operating Procedures
• Previous Good Manufacturing Practice (GMP) experience highly preferred