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QRC Group

Sr Engineer

Juncos, PRPresencialContratoTiempo completo

Publicado 6 oct 2026

We are seeking Sr Engineer with experience in Medical Devices or Pharma industry.

Duties:
1. C&Q Strategy & Planning
  • Develop and implement the overall Commissioning & Qualification strategy aligned with project and regulatory requirements.
  • Define system boundaries and identify direct/indirect impact systems.
  • Lead risk assessments (e.g., ISPE Baseline, ASTM E2500) to determine qualification scope.
  • Develop C&Q plans, schedules, and resource forecasting.
2. Commissioning Activities
  • Oversee and/or execute commissioning activities including FAT, SAT, and field commissioning.
  • Ensure systems are installed and operate per design specifications.
  • Coordinate with vendors and contractors during startup activities.
  • Review and approve commissioning documentation and test results.
3. Qualification Execution (IQ/OQ/PQ)
  • Author, review, and approve qualification protocols (IQ, OQ, PQ).
  • Ensure traceability from User Requirements Specifications (URS) through testing.
  • Execute or oversee protocol execution and ensure proper documentation of results.
4. Documentation & Compliance
  • Ensure all C&Q documentation complies with GMP, FDA, EMA, and internal Amgen standards.
  • Maintain document lifecycle within electronic systems.
  • Support data integrity and ALCOA+ principles throughout qualification activities.
  • Prepare and support validation summary reports.
5. Risk Management & Change Control
  • Lead and document risk assessments related to system qualification.
  • Evaluate and manage change controls impacting validated systems.
  • Assess impact of deviations and implement corrective and preventive actions (CAPA).
6. Cross-functional Coordination
  • Collaborate with Engineering, Validation, Quality Assurance (QA), Manufacturing, and Supply Chain teams.
  • Interface with system owners and technical authorities.
  • Provide technical guidance and mentorship to junior engineers and project team members.
  • Support project meetings, status reporting, and stakeholder communication.
7. Characterization Process
  • Develop the characterization protocols.
  • Execute the characterization activities.
  • Develop and review the characterization reports


Requirements

  • Doctorate or Masters + 2 years of Engineering experience or
    Bachelors in Engineering + 4 years of Engineering experience
  • Bilingual (Spanish/English)



Resumen del puesto

Tipo de empleo

Tiempo completo

Habilidades requeridas

Commissioning & Qualification (C&Q) Strategy and PlanningFactory Acceptance Testing (FAT), Site Acceptance Testing (SAT) and Field CommissioningQualification Protocols (IQ/OQ/PQ) authoring, review and approvalRegulatory compliance with GMP, FDA and EMA requirementsRisk assessment using ISPE Baseline and ASTM E2500 methodologiesChange control and CAPA evaluation and managementElectronic documentation lifecycle managementData integrity and ALCOA+ principles applicationVendor and contractor coordination during startup activitiesCross-functional collaboration and stakeholder communicationTechnical mentorship and guidance to junior engineersCharacterization protocol development, execution and reportingBilingual communication (Spanish/English)

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