Biopharma MRO & Calibration Planner

KBI Biopharma, Inc.; Boulder (CO); Vor Ort; USD 55.000 - 76.000; Vollzeit

Benefits dieser Stelle

Annual bonus structure

Medical, dental, and vision coverage

Paid PTO and holidays

401K matching with 100% vesting in 60 

employee recognition programs

Zusammenfassung

KBI Biopharma, Inc. in Boulder, CO seeks an MRO inventory maintenance and calibration planner level 1 to support equipment maintenance at our biopharma facility.

You will forecast, schedule, and document calibration and maintenance activities using the CMMS and specify parts for planned and unplanned work. Collaborate with maintenance technicians and Facilities Engineering to install critical parts, integrate CMMS with SAP, and improve our MRO program while ensuring cGMP compliance in a

Qualifikationen

• Must have high school diploma or equivalent and 2+ years in a regulated biopharma setting.
• Proficient in MS Office and strong written/verbal communication.
• Solid understanding of cGMP and regulatory compliance.
• Experience with CMMS/asset management and SAP integration is preferred.
• Inventory management and BOM knowledge desirable.

Aufgaben

• MRO inventory management including cycle counting and parts accuracy.
• Maintain and document calibration/maintenance plans in CMMS.
• Integrate CMMS with SAP and help build engineering asset BOMs.

Kenntnisse

MS Office

Verbal & written communication

cGMP knowledge

Inventory management

Team collaboration

Ausbildung

High school diploma or equivalent

Tools

Blue Mountain CMMS

SAP

ETQ

Jobbeschreibung

KBI Biopharma, Inc. in Boulder, CO seeks an MRO inventory maintenance and calibration planner level 1 to support equipment maintenance at our biopharma facility.

You will forecast, schedule, and document calibration and maintenance activities using the CMMS and specify parts for planned and unplanned work. Collaborate with maintenance technicians and Facilities Engineering to install critical parts, integrate CMMS with SAP, and improve our MRO program while ensuring cGMP compliance in a