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Location
In office (Juncos)
Seniority
Principal · 4+ years exp
Employment
Contractor

Confirmed on the employer's own hiring board on Nov 8, 2026. First seen by Alion on Nov 6, 2026.

Overview
Company
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Profile match
QRC Group is a consulting company that provides regulatory compliance, validation, quality systems and technology consulting services to pharmaceutical, medical device and biotechnology manufacturers. Founded in 2005 in Puerto Rico, it places quality assurance, validation, investigation and data science staff at client manufacturing sites across Puerto Rico and the United States. The company is headquartered in Puerto Rico.

QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

Log on now to our website http://www. qrcgroup.com / to learn more about our services and solutions!

Sr Engineer with experience supporting manufacturing equipment and systems in a regulated pharmaceutical or biotechnology environment, with the ability to independently manage technical assessments, corrective actions, and equipment improvement initiatives.

  • Performing System Owner assessments and engineering impact assessments related to equipment failures, process deviations, and quality events.
  • Supporting technical investigations, identifying equipment failure mechanisms, and developing corrective and preventive actions to reduce recurrence.
  • Evaluating the applicability of CAPA and lessons learned to other equipment, systems, and manufacturing areas.
  • Managing engineering activities in IBM Maximo, including work order technical review, pre-approval and post-approval activities, maintenance coordination, and follow-up through closure.
  • Developing and revising preventive maintenance strategies, Job Plans, inspection requirements, and SOPs.
  • Implementing engineering controls and completing actions associated with safety incidents and INCA records.
  • Supporting equipment troubleshooting, repair coordination, replacement of obsolete equipment, spare parts evaluations, and equipment modernization projects.
  • Working with bio pharmaceutical manufacturing equipment such as centrifuges, autoclaves, process tanks, chromatography and UF/DF systems, homogenizes, filter integrity testers, and associated instrumentation.
  • Preparing clear technical reports and assessment rationales, maintaining traceable supporting documentation, and completing actions within established deadlines.
  • Coordinating with Manufacturing, Process Engineering, Maintenance, Quality, Automation, Validation, and equipment suppliers.
  • Managing multiple concurrent assignments and prioritizing work according to safety, quality, and operational needs..
  • Doctorate or Masters + 2 years of Engineering experience or

    Bachelors in Engineering + 4 years of Engineering experience (Chemical, Mechanical or Electrical Engineer)

  • Bilingual (Spanish/English)

All your information will be kept confidential according to EEO guidelines.

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