Maintenance Mechanic III, Utilities

CSL Plasma

Holly Springs (NC)

Sur place

USD 70 000 - 95 000

Plein temps

14 jours+
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Résumé du poste

CSL Plasma is seeking an experienced Maintenance Technician to oversee maintenance and operation of site boilers, chillers, and waste systems in a cGMP biotechnology environment. The role requires collaboration with Utilities Maintenance, Process Engineering, and Quality to ensure GMP compliance and efficient equipment performance.

You will perform corrective and preventive maintenance, develop maintenance plans, manage spare parts, and coordinate with internal and external stakeholders to

Qualifications

  • Advanced experience in maintenance within cGMP biotech/pharma manufacturing.
  • Knowledge of DCS/PLC and BAS control systems.
  • Experience with CMMS and regulatory compliance.
  • Strong problem-solving and organizational skills.

Responsabilités

  • Collaborates with Utilities Maintenance, Process Engineering, and Quality to ensure GMP compliance.
  • Performs corrective and preventive maintenance on site utilities equipment.
  • Develops maintenance plans and work instructions for site equipment.
  • Oversees contract service providers during maintenance execution.
  • Responds to facility alarms and initiates corrective actions.
  • Coordinates maintenance activities with internal stakeholders to minimize disruptions.

Connaissances

GMP experience
Troubleshooting
Maintenance planning
Communication skills

Formation

High School Diploma
Associate degree

Outils

CMMS (SAP)
BAS/PLC
DCS/PLC control systems
Building Automation Systems

Description du poste

Reporting to a Maintenance Manager / Supervisor/Lead, incumbent will be responsible for the maintenance and operation of Utility equipment (GMP and non-GMP) site Boilers, Chillers and Waste systems. Incumbent will be a key shop floor contributor, providing independent support and execution of maintenance tasks.

Hours - Wednesday, Thursday, Friday, and every other Saturday. Nights - 6pm - 6am

Responsibilities
  • Collaborates with Utilities Maintenance, Process Engineering, and Quality teams to ensure work activities are compliant with GMP guidelines and regulatory requirements.
  • Performs corrective and preventive maintenance on Clean and Dirty equipment that provide uninterrupted Utilities for the site.
  • Develop efficient maintenance job plans, procedures, and work instructions for site equipment.
  • Recommends spare parts and preventive maintenance procedures to optimize equipment reliability.
  • Routes documentation for spare parts requests and work order submissions.
  • Assists other departments in troubleshooting, testing, repairing, and optimizing equipment performance.
  • Contributes to continuous improvement initiatives within the site's Maintenance Program.
  • Responds promptly to facility alarms and initiates appropriate corrective actions.
  • Coordinates maintenance activities with internal stakeholders to minimize operational disruptions.
  • Oversees contract service providers and support contractors during maintenance execution.
  • Demonstrates proficiency with tools and software such as CMMS (SAP) BAS, PAS, Pi, and PLCs.
Experience
  • Advanced experience and knowledge of maintenance disciplines within a cGMP Biotechnology / Pharmaceutical manufacturing environment.
  • Demonstrated knowledge of DCS, PLC, and/or Building Automation Systems (BAS) control systems.
  • Proven knowledge of a Computerized Maintenance Management System (CMMS).
  • Working knowledge of the process for fermentation, purification, utilities and formulation preferred.
  • Demonstrated experience problem solving and troubleshooting systems in a pharmaceutical environment required.
  • Strong organizational and planning skills required.
  • Excellent interpersonal effectiveness and communication skills (written and oral) are required in order to interface across management levels and departments.
Education
  • High School Diploma with 5+ years' relevant GMP / industry experience OR an Associate degree with 4+ years' relevant GMP / industry experience OR equivalent.
  • Different qualifications or responsibilities may apply based on local legal and/or educational requirements.
  • Refer to local job documentation where applicable.
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