Senior Mechanical Engineer – Pharma HVAC & Cleanrooms

Jedson Engineering

San Juan (PR)

Vor Ort

USD 120.000 - 170.000

Vollzeit

Vor 5 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Zusammenfassung

Jedson Engineering seeks a Registered Professional Mechanical Engineer to lead HVAC design for pharmaceutical process facilities, including cleanrooms, labs and process suites. The role emphasizes cGMP awareness, contamination control, and coordination with process, automation and construction teams.

The ideal candidate has a strong background in cleanroom environments, aseptic processing, regulatory compliance, and experience supporting commissioning and qualification activities.

Qualifikationen

  • Bachelor degree in Mechanical Engineering required.
  • Active PE licensure is required.
  • 10+ years in pharma/biotech or life sciences facilities.
  • Experience with pharmaceutical HVAC, cleanrooms and aseptic processing.
  • Experience supporting commissioning and qualification activities.
  • Proficiency with design tools; AutoCAD/REVIT preferred.

Aufgaben

  • Design and oversee HVAC systems for pharmaceutical manufacturing, labs, cleanrooms and process suites.
  • Develop mechanical packages including load calculations and airflow strategies.
  • Coordinate with process eng, validation, QA, automation and construction.
  • Lead or support commissioning, qualification and validation activities.
  • Review submittals, drawings, and calculations; drive energy efficiency improvements.
  • Support audits, inspections, and regulatory reviews.

Kenntnisse

HVAC design
Cleanroom design
Aseptic manufacturing support
Building automation systems
Commissioning & qualification
Autocad/REVIT
Technical writing & coordination

Ausbildung

Bachelor degree in Mechanical Engineering
PE license

Tools

Autocad
REVIT

Jobbeschreibung

Jedson Engineering seeks a Registered Professional Mechanical Engineer to lead HVAC design for pharmaceutical process facilities, including cleanrooms, labs and process suites. The role emphasizes cGMP awareness, contamination control, and coordination with process, automation and construction teams.

The ideal candidate has a strong background in cleanroom environments, aseptic processing, regulatory compliance, and experience supporting commissioning and qualification activities.

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