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Maintenance Planner (cGMP - CMMS - Pharmaceutical) JD816669

JD816669

DPS Engineering is looking for an experienced Maintenance Planner/CMMS Specialist to work with a BioPharma client in the Boston, MA area. This individual will perform the scheduling of maintenance activities with respect to any maintenance processes related to the quality system. The ideal candidate should be able to plan work with awareness of associated audits, notice of events, equipment change control, day-to-day activities and maintenance outsourcing. This person should also have a strong understanding of GMP manufacturing environments.

Category:
Schedules Personnel
Location:
Massachusetts
Years of Experience Req.:
2+
Date Posted:
01/01/2019
Days Remaining:
39
Employment Type:
Full-time
Education Level Req.:
Bachelors Preferred

Maintenance Planner (CMMS - Pharmaceutical)        JD816669

Boston, MA area

 

Summary:

 

DPS Engineering is looking for an experienced Maintenance Planner to work with a BioPharma client in the Boston, MA area. This individual will perform the scheduling of maintenance activities with respect to any maintenance processes related to the quality system. The ideal candidate should be able to plan work with awareness of associated audits, notice of events, equipment change control, day-to-day activities and maintenance outsourcing. This person should also have a strong understanding of GMP manufacturing environments.

 

Responsibilities:

  • Develop and plan accurate and concise scopes of work for corrective work orders, drawing upon internal and/or external expertise.
  • The day-to-day ability to map work priorities and work assessment to the manufacturing plan (i.e. planned preventive maintenance work orders and work backlog).
  • Gather required information to be decisive in moving work requests through the planning & scheduling process.
  • Formaliz750399.283952e work plan as well as a 30 day forecast of maintenance activities.
  • Publish to customers and maintenance personnel the agreed to date for the work to be performed and systems returned to service.
  • Develop positive and cooperative working relationships between the facilities operations groups and the customer manufacturing and R & D groups.
  • Research and supply information and technical data for securing spare parts.
  • Work in a collaborative team environment and interact with other support groups such as Engineering, Validation, Quality Assurance and Metrology.
  • Complete and provide accurate documentation, as required in cGMP operations.

 

Qualifications and Education: 

  • Bachelor’s degree in Engineering, Science or a related discipline is preferred.
  • 2+ years’ planning/scheduling related experience as well as 3+ years of experience in cGMP or regulated industry.
  • Proven proficiency with computer skills utiliz750399.283952ing MS Office suite as well as experience working with MS Project and Computeriz750399.283952ed Maintenance Management Systems (CMMS).
  • Excellent written and verbal communication skills.
  • Experience using TrackWise, Livelink, Plateau or other quality management systems.
  • Experience working independently under little supervision in a team environment.
  • Experience with Infor Enterprise Asset Management Software (Infor EAM) is preferred.
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