Pharmaceutical Manufacturing Operator I
Catalent, Kansas City, MO, Onsite
Manufacturing ProductionHigh School RequiredEntry Level
Catalent, Kansas City, MO, Onsite
Work Schedule: Monday – Thursday 1:30pm-12am
100% onsite
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
High school diploma or GED required
0-3 years of experience with Pharma or cGMP manufacturing environment preferred.
Equipment process and framework knowledge. Have 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