More jobs:
Metrologist
Job in
Durham, Durham County, North Carolina, 27703, USA
Listed on 2026-06-10
Listing for:
MedPharm Ltd
Full Time
position Listed on 2026-06-10
Job specializations:
-
Quality Assurance - QA/QC
Quality Engineering -
Manufacturing / Production
Quality Engineering
Job Description & How to Apply Below
This position contributes to the company success by providing calibration and instrumentation oversight for lab equipment through executing scheduled calibrations and preventative / corrective maintenance in compliance with GMP regulations and internal procedures.
Summary ofKey Responsibilities
- Maintain and perform corrective, preventative maintenance calibrations on GMP and non-GMP equipment
- Performs maintenance, testing, troubleshooting, calibration, and repair of electrical circuits, components, analytical instruments, and pharmaceutical laboratory and manufacturing equipment.
- Maintains all logs and required documentation.
- Writes Out-Of-Tolerances (OOT’s) and Deviations.
- Disassembles and reassembles instruments and equipment, using hand tools, and inspects instruments and equipment for defects.
- Entering and updating CMMS system information relevant to calibrations performed
- Provide recommendations for instrumentation / metrology spare parts and PM procedures
- Work closely with Validations and Stability Manager, Lab Operations, Manufacturing and Quality to ensure strict compliance with GMP guidelines, specifically to ensure that equipment is maintained in GMP compliance
- Assist in the maintenance and review of calibration standards and vendor calibration documentation
- Work with contract service providers and support contractors executing calibration and metrology activities
- Provide support to other departments to troubleshoot, test, repair and optimize instruments, equipment and control systems
- Provide support for IQ/OQ and PQ of new systems throughout the facility
- B.S., in a scientific or engineering discipline, with 2-5 years of relevant GMP pharmaceutical experience, or an Associate's Degree in a relevant technical discipline with 5+ years of GMP pharmaceutical or equivalent
- Knowledge of current industry expectations of validation requirements for equipment validation and qualification
- Technical ability to problem solve and troubleshoot equipment systems in a pharmaceutical environment, including but not limited to: HPLCs, balances, pH meters, HVAC, chart recorders and stability chambers
- Flexibility to work outside of business hours, should issues arise
- Knowledge of Quality systems
- Speaks, writes, listens and presents information in a logical and articulate manner appropriate for the audience
- Able to multi-task productively, well organized, effectively applies time management processes and procedures
- Ability to recognize what needs to be done, taking action, and accomplishing results as the situation demands
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