Validation Specialist â Equipment
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Job Location:
Barceloneta - USA
Monthly Salary:
Not Disclosed
Posted on:
14-09-2025
Vacancies:
1 Vacancy
Job Summary
Validation Specialist Equipment
Location: Barceloneta Puerto Rico (On-site)
Shift: Day (7:00 a.m. 5:00 p.m.)
Start: ASAP
Role Overview
Execute and support validation for new and existing equipment partnering closely with Construction Utilities Operations and Quality. You will prepare/execute protocols assess project impacts and ensure inspection-ready documentation and safe compliant start-ups.
Key Responsibilities
Plan and execute equipment validation activities aligned to construction/utilities work in cleanrooms.
Coordinate with area owners on documentation materials and training; maintain change and deviation records.
Generate and maintain validation packages (protocols reports traceability risk assessments) and supporting logs.
Support readiness for start-up walk-downs and handover; address gaps to meet regulatory expectations.
Adhere to EHS/Security cGMP and site procedures; provide precise status and metrics.
Minimum Qualifications
Bachelors degree preferred (Engineering Science or related) or equivalent experience.
Validation experience in pharma or highly regulated manufacturing; cleanroom familiarity.
Strong collaboration with PM/Field teams; excellent written and verbal communication.
Proficiency with MS Office and basic schedule/document tools; day-shift availability (75).
Preferred
Exposure to commissioning/qualification interfaces (e.g. IQ/OQ/PQ) risk tools (FMEA/pFMEA) and data integrity practices.
Onboarding
One day of on-site training; computer/system access to follow.
Required Experience:
Unclear Seniority
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