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United Therapeutics Corporation

Biotech company develops PAH therapies

GMP Maintenance Technician 2 / Senior GMP Maintenance Technician

Equipment MaintenanceConfirmed live in the last 24 hours
Full-timeDurham, NC, USANo salary listed

About the Job

Requirements

  • A high school diploma or General Education Degree (GED) is required.
  • For GMP Maintenance Technician II level, a minimum of 4 years of experience as maintenance personnel in an industrial, pharmaceutical/biotechnology, or manufacturing environment is required.
  • For Senior GMP Maintenance Technician level, a minimum of 6 years of experience as maintenance personnel in an industrial, pharmaceutical/biotechnology, or manufacturing environment is required.
  • Proficiency in all Microsoft Office applications is required.
  • Experience troubleshooting and repairing pneumatic, electronic, and hydraulic control systems, including diagnosing non-routine issues, is required.
  • Working knowledge of test equipment such as digital voltmeters, temperature probes, and pneumatic calibrators is required.
  • Strong organizational and problem-solving skills are required.
  • Written and verbal communication skills sufficient to communicate effectively across functions and with external vendors are required.
  • The ability to provide guidance or technical support to less experienced technicians is required.

Responsibilities

  • Execute planned and unplanned routine maintenance and repairs on manufacturing, filling, assembly, and packing/kitting lines to ensure efficient production and supply of Tyvaso DPI medicine.
  • Work closely with Mechanics team members to complete maintenance events on time, document events in a Computerized Maintenance Management System (CMMS), and maintain an accurate spare parts inventory.
  • Assist with equipment operations and work with stakeholders and vendors to anticipate and resolve mechanical and automated equipment issues while adhering to current Good Manufacturing Practices (cGMPs).
  • Understand the role equipment and systems play in meeting Critical Process Parameters (CPPs), certificate of pharmaceutical product requirements, and other regulatory guidelines in DPI manufacturing and kitting operations.
  • Perform preventative maintenance on equipment and update BMRAM to maintain accurate records with limited supervision.
  • Troubleshoot and diagnose mechanical, electrical, and operational issues on production equipment, using technical judgment to resolve non-routine issues and ensure problems are addressed promptly and effectively.
  • Maintain proficiency in GMP maintenance responsibilities and apply working knowledge to improve equipment performance and reliability.
  • Assist with obtaining maintenance proposals, approving purchase orders, and procuring spare parts inventory from external vendors to support DPI manufacturing and kitting equipment.
  • Coordinate with external vendors during site visits to perform maintenance activities on production equipment.
  • Support quality events, deviations, change controls, CAPAs, and action items in TrackWise related to DPI manufacturing and kitting, including investigations and follow-up actions.
  • Support completion of validations, special projects, audits, and other requirements, contributing to execution and documentation; this may include travel to other United Therapeutics or vendor sites.
  • Perform other duties as assigned.

Desired Qualifications

  • An associate degree in life science, mechanical studies, or technical vocational studies in a related field is preferred.
  • Experience with automation systems and platforms is preferred.
  • Advanced ability to troubleshoot and operate complex automation systems and resolve non-routine issues is preferred.
  • Experience using a regulated database such as BMRAM or Cal Man is preferred.
  • Four or more years of experience in the pharmaceutical or medical devices industry is preferred.

About the Company

United Therapeutics Corporation

Biotech company develops PAH therapies

United Therapeutics develops medicines for pulmonary arterial hypertension and other rare diseases, and pursues organ manufacturing through its Xenotransplantation efforts. Its drugs are given as oral tablets, intravenous infusions, or inhaled therapies to open damaged lung vessels and support heart function, while its organ programs aim to create bioengineered organs from donor animals to reduce rejection. The company differentiates itself by pairing a pharmaceutical portfolio with regenerative medicine and organ manufacturing, and by operating as a public-benefit corporation with sustainable facilities. Its goal is to end the organ transplant shortage by supplying transplantable organs while improving patient outcomes through better drug delivery and regenerative medicine.

Company size
Not listed
Company stage
IPO
Headquarters
Silver Spring, MD
Founded
1996

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