Metrologist

Posted 8 Days Ago
Be an Early Applicant
Durham, NC, USA
In-Office
Mid level
Biotech • Pharmaceutical
The Role
Perform calibration, preventative and corrective maintenance, testing, troubleshooting, and repair of laboratory and GMP manufacturing instrumentation. Maintain logs and CMMS records, write OOTs and deviations, support IQ/OQ/PQ activities, coordinate with validations, quality, R&D and contractors, and ensure instrumentation fitness and compliance across GMP and non-GMP sites.
Summary Generated by Built In

Job Purpose: This position contributes to company success by providing calibration and instrumentation oversight for laboratory and facility equipment across MedPharm’s Durham sites, including the Stirrup Creek GMP manufacturing facility and the Emperor Boulevard R&D laboratories. The role executes scheduled calibrations and preventative / corrective maintenance in compliance with GMP regulations, internal procedures, and research laboratory requirements, ensuring equipment is maintained in a state of control and fitness for intended use across both regulated and non-GMP environments.

Summary of Key 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, R&D scientific teams (Emperor Boulevard, Manufacturing and Quality to ensure strict compliance with GMP guidelines, specifically to ensure to ensure instrumentation remains compliant and fit-for-purpose across both GMP and non-GMP operations
  • Support calibration, maintenance, and troubleshooting of instrumentation across both GMP and R&D environments, including bioanalytical, research biology, and in vitro testing at the Emperor Boulevard R&D site
  • Ensure instrumentation readiness, uptime, and compliance across two distinct operational environments: GMP-regulated manufacturing and non-GMP research laboratories 
  • 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

Required Qualifications and Skills:

  • 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

Supervisory Responsibility:

Direct Reports:            None

Indirect Reports:         None

Confidential Data:      Yes 

Travel Requirements:  Limited local travel between Durham sites 

Work Environment:  Climate controlled office and laboratory.   
        

All position requirements listed indicate the minimum level of knowledge, skills and/or experience necessary to perform the job proficiently.  This position description is not to be construed as an exhaustive statement of duties, responsibilities or requirements.  Employees will be required to perform any other job-related duties as requested by their supervisor, subject to reasonable accommodation.

Skills Required

  • B.S. in a scientific or engineering discipline with 2-5 years of GMP pharmaceutical experience, or associate's degree with 5+ years of GMP pharmaceutical or equivalent
  • Knowledge of equipment validation and qualification requirements (IQ/OQ/PQ)
  • Technical troubleshooting and maintenance experience with HPLCs, balances, pH meters, HVAC, chart recorders, and stability chambers
  • Experience performing calibrations, preventative and corrective maintenance, and maintaining calibration documentation and logs
  • Experience entering and updating information in a CMMS
  • Knowledge of Quality systems and GMP regulations
  • Ability to write Out-Of-Tolerance reports and deviations
  • Ability to work outside normal business hours when needed
  • Strong communication, organization, multitasking, and problem-solving skills
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The Company
HQ: Guildford
230 Employees
Year Founded: 1999

What We Do

MedPharm is a world-leading contract provider of topical and transdermal product design and development services. Our delivery of robust and innovative research has commanded recognition from regulators and investors alike. We utilise our unique cost-effective performance testing models to mitigate risk and accelerate development times.

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