Quality Control Specialist

KOCH INDUSTRIES INC • Hudson, WI • 1d ago

JOB REQUIREMENTS: Your Job Phillips Medisize, a Molex company is seeking
a Drug Logistics Material Specialist to join our team at our Hudson, WI
site. In this role, you will play a vital role in maintaining the
accuracy and compliance of drug product inventory within
temperature-controlled environments. This role offers the opportunity to
contribute innovative solutions to optimize drug logistics operations
within a dynamic pharmaceutical manufacturing environment. Our Team
Phillips Medisize is an end-to-end provider of innovation, development,
and manufacturing solutions to the pharmaceutical, diagnostics and
medical device industries. Our team at Hudson, WI is made up roughly of
300 employees that support our production, Engineering, Quality, Molding
& Tooling departments. What You Will Do Ensure all drug products are
accurately tracked entering and leaving storage areas, keeping records
audit-ready and compliant with regulatory standards. Collaborate with
project teams to complete all required documentation for new or updated
products, including chemical reviews, hazard worksheets, inventory
forms, and impact assessments. Work closely with project teams,
warehouse, operations, and engineering to facilitate smooth product
receipt, staging, and readiness for processing. Monitor inventory
levels, fulfill drug requests promptly, and coordinate with purchasing
to maintain optimal stock, including related materials such as data
loggers and transport carts. Manage timely receipt and proper storage of
drug products, prioritize urgent items to prevent delays, and prepare
finished products for shipment following all compliance protocols.
Perform regular temperature mapping and monitoring of drug storage
locations (including coolers), ensuring adherence to temperature
standards and coordinating with calibration teams. Conduct regular
inventory cycle counts, investigate discrepancies, and execute ERP
system transactions to maintain real-time inventory status and accurate
labeling. Maintain organization and segregation of walk-in cold rooms
and drug storage areas per FIFO, quarantine, rejected, and approved
classifications. Ensure all procedures are standardized, consistently
applied, and documented; develop innovative solutions to address
operational challenges and unforeseen issues. Who You Are (Basic
Qualifications) 3+ years of experience in quality within the
pharmaceutical, medical device, or biotechnology industry 2+ years of
direct experience in drug manufacturing Experience in quality management
tools, methodologies (e.g. risk management, root cause analysis, FMEA),
and software systems What Will Put You Ahead Ability to work effectively
with cross-functional teams such as Quality Engineers, Manufacturing
Engineers, and Operations. Experience with tracking TOR (Time Out of
Refrigeration) for drug... For full info follow application link. Equal
Opportunity Employer, including disability and protected veteran status.
*** APPLICATION INSTRUCTIONS: Apply Online:
ipc.us/t/3ECEA3E9C3A5477A

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Minnesota Visiting Nurse Agency • Minneapolis, MN • 14h ago

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14h ago

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Registration Specialist Senior, Admitting and Registration

Minnesota Visiting Nurse Agency • Minneapolis, MN • 14h ago

IT & Engineering

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14h ago

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ECOLAB INC • Hudson, WI • 19h ago

IT & Engineering

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19h ago

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Aerotek • Saint Paul, MN • 21h ago

IT & Engineering

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