Quality Control Technician I

Catalent Pharma Solutions•Kansas City, MO

7d•Onsite

About The Position

Quality Control Technician I Position Summary Shift: Monday – Friday 12pm - 8pm 100% on-site Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. The Quality Control Technician I performs tasks from detailed instructions and established procedures. Comply with site SXPs, corporate policies, and Environmental Health and Safety requirements. Applies technical skills and strong work habits to complete assigned work within own group/project team. A self-motivated, detail-oriented person who is able to make decisions and solve problems is essential. Able to work independently with little supervision, and flexible to also assist team members as needed.

Requirements

High School diploma or equivalent with zero (0) years of experience
Mathematical and scientific reasoning ability and ability to learn and retain technical information
Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form
Excellent written and verbal communications skills with internal customers, team members, and management
Strategy is focused on personal time management and efficiency
Individual may be required to sit, stand, walk regularly and occasionally lift, pull or push 0-40 pounds

Responsibilities

Physically receive and count, sort, label, and organize samples by lot/condition/sample orientation for the purposes of stability study setups and/or pulls
Communicate effectively with internal (project management, operations, and laboratory personnel) and external customers to facilitate efficient sample flow
Assist with sample set downs, staging, pulling and sample movements.
May obtain DEA clearance and participate in controlled substance inventory verification
Perform labware cleaning, including but not limited to physical receipt, organization, loading and unloading glassware washers, and inspection of labware (chips or cracks)
May order and receive compressed gas cylinders required for the labs. May monitor cylinder inventory and verify accuracy of order upon delivery
Maintain high quality documentation in accordance with applicable regulatory guidance and site SOPs documenting work as appropriate within notebooks, forms, etc.
Execute procedures or methods with high quality and review own work to ensure accuracy and completeness and able to identify minor quality/compliance gaps during routine work

Benefits

Competitive medical benefits and 401K
152 hours PTO + 8 Paid Holidays
Dynamic, fast-paced work environment
Opportunity to work on Continuous Improvement Processes
Catalent offers rewarding opportunities to further your career!
Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world.
Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us.
Join us in making a difference. personal initiative. dynamic pace. meaningful work.

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