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Cleanroom Fill Technicians (Multiple Shifts)

Fagron Sterile Services

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At a glance

Compensation
No compensation found
Location
Wichita, KS
Work Authorization
Not specified

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Job overview

The Cleanroom Fill Technician assembles sterile products, maintains a CGMP‑compliant cleanroom, and ensures equipment validation while documenting batch records and coordinating supplies. The role requires strict adherence to sterility protocols, inventory management, and timely shift attendance, supporting patient safety and product quality in a regulated manufacturing environment.

Skills & qualifications

RequiredNice to have

Skills

Cleanroom ProceduresCGMP ComplianceWork With OthersTake InitiativeStrong Attention to DetailPrioritize and Plan Work ActivitiesHandle Multiple Tasks

Qualifications

High School Diploma or Equivalent1-4 Years Previous Work Experience in Hospital or Manufacturing Environment or Aseptic Filling

Full job description

This job was posted by https://www.kansasworks.com : For more information, please see: https://www.kansasworks.com/jobs/13654139 ## Who We Are Since 1990, weve grown into a global leader in personalized medicine. Today, our +5,000 energetic employees are based in +80 locations in Europe, North America, South America, Africa and Asia-Pacific and are working together to support over 200,000 customers worldwide. From compounding and natural products to software, equipment, and genomics we deliver smart, ready-to-use solutions that make healthcare better. Were passionate, science-driven, and always looking for new ways to improve lives. ?? Explore your future atFagron Career Site. ## About The Job [The Cleanroom Fill Technician will assemble finished sterile products with a focus on patient safety and quality; ensure that the clean room remains in a state of constant cleanliness and that supplies are appropriately stacked.]{contrast="auto"} [Key Responsibilities]{contrast="auto"} - [Maintains a sterile environment in the cleanroom, by garbing, cleaning the room, and behaving according to clean room procedures that align with CGMP practices or guidelines.]{contrast="auto"} - [Cleans the equipment in the cleanroom daily; ensures equipment validations are up to date.]{contrast="auto"} - [Follows the tech check tech process to oversee the techniques and practices of co-workers, including product assembly, measurements, garbing, sterile techniques, and documentation.]{contrast="auto"} - [Take inventory into the cleanroom to identify components needed to fill production batches, as scheduled.]{contrast="auto"} - [Ensure all components entering the clean room are sterile.]{contrast="auto"} - [Coordinates and communicates with compounding and vial wash to obtain supplies needed to turn products; communicates within the clean room, from room to room.]{contrast="auto"} - [Documents batch records, Climents (measurements of air in the room), lumacs (log use, maintenance, and cleaning of all equipment), and cleaning logs.]{contrast="auto"} - [Prepares and sterilizes components/vials for appropriate solutions; sterilizes solutions and fills into specified containers.]{contrast="auto"} - [Validates that garbing standards have been followed on a semi-annual basis.]{contrast="auto"} - [Completes 3 consecutive media fills with a set minimum of syringes and vials that is established by the quality department in an established time frame and in the most difficult operating conditions to pass validation every 6 months.]{contrast="auto"} - [Follows standard operation procedures to package sterile products in their final container closure.]{contrast="auto"} - [Designate people and hoods for different tasks.]{contrast="auto"} - [Use appropriate process to establish sterility on products received via pass through from compounding.]{contrast="auto"} - [Clock in and out for every scheduled shift in a timely manner.]{contrast="auto"} ## Basic Qualifications [High school diploma or equivalent; one to four years previous work experience in a hospital or manufacturing environment or doing aseptic filling.]{contrast="auto"} [Knowledge of cleanroom procedures preferred but not required.]{contrast="auto"} [Knowledge of and compliance with CGMP (Current Good Manufacturing Practices) regulations preferred but not required.]{contrast="auto"} [Must pass validation three consecutive times before handling product in clean room; must be re-qualified every 6 months with a minimum requirement of filling a set minimum of syringes and vials in an established time frame and difficult operation conditions. Preferred but not required.]{contrast="auto"} [Ability to work with others in a positive and professional manner and to develop and maintain strong working relationships with co-workers and management.]{contrast="auto"} [Ability to take initiative, including asking for and offering help when needed; performs work independently without being prompted.]{contrast="auto"} [Strong attention to detail and focus on quality, accuracy, sterility, and aseptic technique.]{contrast="auto"} [Ability to prioritize and plan work activities. Manages time effectively and adapts quickly to changing priorities.]{contrast="auto"} [Ability to handle multiple tasks and organize re ]{contrast="auto"}

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