Pharmaceutical Manufacturing Operator I

Catalent•Kansas City, MO

1d•Onsite

About The Position

Start your career where science meets purpose. At Catalent, we don’t just make medicine—we help people live better, longer lives. As a Pharmaceutical Manufacturing Operator I, you’ll be part of a team that transforms scientific breakthroughs into life-saving treatments. This is more than a job. It’s a career launchpad in a growing industry with real impact. The Role Responsible for ensuring cGMP compliance, general good housekeeping, informing Senior Pharmaceutical Technician or Pharmaceutical Manufacturing Lead of work orders to be placed for processing rooms and equipment within core group. Ensures 5S standards are met and maintained. Ensure that the facility is kept “tour ready” at all times and people/material/flow/cleaning and zone concepts are maintained at all times. Associate Pharmaceutical Technician should have high ability to learn batch records to ensure clarity and drive accuracy for processing. Ensure that training is up to date and progressing for core group requirements with direction from Senior Pharmaceutical Technician or Pharmaceutical Manufacturing Lead. Ensure that assigned operational areas are processing under GMP conditions and applicable SOP’s are being strictly followed. Provides information to support core group metrics and efficiency increases. Focuses on building proficiency with business critical equipment within core group while maintaining high quality standards. Follows all Catalent safety procedures and identifies/communicates the necessary adjustments to address potential safety concerns. Will also ensure the proper use of PPE (Personal Protection Equipment) Ability to wear a PAPR (Powered Air Purifying Respirator) during manufacturing when required. Ability to wear required gowning required to work in the GMP manufacturing areas. Operating safely in a dynamic environment which includes mobile and fixed equipment and changing conditions while completing job tasks that range from simple to complex and/or multi-tasking. Must be capable of wearing steel-toed safety shoes for 8 to 12 hours a day, depending on duration of the shift. Other duties, as assigned

Requirements

High school diploma or GED required
0-3 years of experience with Pharma or cGMP manufacturing environment preferred
Equipment process and framework knowledge
Working knowledge of basic hand tools
Basic computer skills
Knowledge of cGMP, FDA, MHRA and DEA guidelines and how to apply them effectively
Knowledge of Solid Dosage manufacturing preferred
Must be able to manage priorities and projects prioritizing effectively
Capability to work in a matrix organization
Maintains current knowledge of cGMP regulations and regulatory trends as they pertain to the stated responsibilities
Individuals may be required to sit, stand, walk regularly and occasionally lift up to 40 pounds

Responsibilities

Ensuring cGMP compliance
General good housekeeping
Informing Senior Pharmaceutical Technician or Pharmaceutical Manufacturing Lead of work orders to be placed for processing rooms and equipment within core group
Ensuring 5S standards are met and maintained
Ensuring the facility is kept “tour ready” at all times
Maintaining people/material/flow/cleaning and zone concepts at all times
Learning batch records to ensure clarity and drive accuracy for processing
Ensuring training is up to date and progressing for core group requirements
Ensuring assigned operational areas are processing under GMP conditions and applicable SOP’s are being strictly followed
Providing information to support core group metrics and efficiency increases
Building proficiency with business critical equipment within core group while maintaining high quality standards
Following all Catalent safety procedures
Identifying/communicating necessary adjustments to address potential safety concerns
Ensuring the proper use of PPE (Personal Protection Equipment)
Ability to wear a PAPR (Powered Air Purifying Respirator) during manufacturing when required
Ability to wear required gowning required to work in the GMP manufacturing areas
Operating safely in a dynamic environment which includes mobile and fixed equipment and changing conditions while completing job tasks that range from simple to complex and/or multi-tasking
Capable of wearing steel-toed safety shoes for 8 to 12 hours a day, depending on duration of the shift