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Metrology Supervisor (cGMP – Pharmaceutical) JD818783

JD818783

DPS is seeking a Metrology Supervisor for a position supporting cGMP manufacturing. This individual will be responsible for managing calibrations in our cGMP manufacturing facility. Individual is expected to perform job functions and responsibilities independently and with limited direction.

Category:
Mechanical
Location:
Massachusetts
Years of Experience Req.:
8+
Date Posted:
15/06/2019
Days Remaining:
18
Employment Type:
Full-time
Education Level Req.:
Bachelors Preferred

Metrology Supervisor (cGMP – Pharmaceutical)                         JD818783

Boston, MA

 

DPS is seeking a Metrology Supervisor for a position supporting cGMP manufacturing.  This individual will be responsible for managing calibrations in our cGMP manufacturing facility.  Individual is expected to perform job functions and responsibilities independently and with limited direction.

 

Responsibilities:

  • Management and oversight of calibration contract service providers.
  • Scheduling of calibration and maintenance activities through coordination with end user groups.
  • Execution of work orders using the computeriz590901.105061ed maintenance management system.
  • Identify and remove single points of failure for calibration activities.
  • Lead process and equipment troubleshooting to support deviations, corrective actions and related issues.
  • Develop and revise Metrology Procedures.
  • Act as Metrology subject matter expert for change management assessments, deviation and CAPA management.
  • Generate and provide quality metrics for site and department.
  • Participate in internal and external audits.
  • Coordinate specification, fabrication, procurement, installation, engineering start-up and validation activities of new equipment and systems.

 

Qualifications and Experience:

  • Bachelor’s degree in science or engineering or related field.
  • Minimum 8 years of experience in a biotech or pharmaceutical company.
  • Experience in design and specification requirements of pilot and commercial scale equipment for pharmaceutical manufacturing.
  • Knowledge and experience with the FDA requirements for clinical and commercial products.
  • Understanding of process controls and equipment automation.
  • Demonstrated project management skills.
  • Ability to work in fast-paced manufacturing environment.
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