Calibration Tech II

United Therapeutics Corporation-posted about 1 month ago
Full-time • Mid Level
Onsite • Raleigh, NC
1,001-5,000 employees
Professional, Scientific, and Technical Services
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The Calibration Technician II will perform calibration, maintenance, and documentation of manufacturing equipment and instrumentation within a manufacturing facility. All duties must be performed in compliance with established policies and procedures in a cGMP-regulated facility.

  • Perform, or oversee vendors performing, calibration of equipment, instruments, or systems in accordance with SOPs in order to reduce interruptions in the daily manufacturing schedules
  • Perform basic to moderate troubleshooting and repair of instrumentation and related equipment or systems, escalating and seeking guidance on most complex tasks
  • Complete proper documentation related to scheduled and unscheduled calibration events on all critical instrumentation and maintain records as required
  • Assist in administering a computerized program that tracks calibration of all equipment associated with CGMP equipment and systems
  • Assist with the writing or revising of SOPs, initiation of calibration protocols, deviation / failure investigations, and creation of reports, etc
  • Assist with equipment validation activities associated with CGMP process
  • Assist with maintaining spare parts inventory
  • Review work performed by other staff, communicate problems and deficiencies, elicit corrections, and enforce company policy and procedures as they relate to calibration requirements
  • Provide training to lower-level technicians on general and specific calibration procedures to support manufacturing operations in order to minimize downtime or delays
  • H.S. Diploma or General Education Degree (GED)
  • 4+ years of experience in a pharmaceutical, food, or chemical manufacturing environment as a calibration technician or equivalent role (is it a requirement for the experience to be in a pharmaceutical, food, or chemical manufacturing environment
  • Ability to become skilled in the use of calibration manager software
  • Strong working knowledge of CGMP regulations
  • Applied knowledge of pharmaceutical GMPs, FDA guidelines, and industry standards and the ability to apply GMP to company specific processes and products
  • Strong professional documentation skills
  • Ability to interact with other departments effectively
  • Ability to handle confidential company data, projects, information, etc.
  • Proficient in Microsoft office or equivalent
  • Strong written and verbal communication skills with the ability to objectively, accurately, and thoroughly convey complex issues in writing and produce a large volume of written materials independently
  • Associate Degree in engineering, life sciences, or other related technical field or equivalent military training and four years of instrumentation experience or the equivalent combination of education and experience
  • Knowledgeable in the use of Kaye data logging equipment and associated computer programming
  • Eligible employees may participate in the Company's comprehensive benefits suite of programs, including medical / dental / vision / prescription coverage, employee wellness resources, savings plans (401k and ESPP), paid time off & paid parental leave benefits, disability benefits, and more.
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