QRC Group, LLC
Sr Engineer
Juncos, PRVor OrtVertragVollzeit
Veröffentlicht am 26. Aug. 2026
Diese Stelle wird in ES ausgeschrieben
We are seeking Sr Engineer with experience in Medical Devices or Pharma industry.
Duties:
1. C&Q Strategy & Planning
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.
- 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.
- 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.
- 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.
- 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).
- 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.
- 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)
Rollenübersicht
Jobart
Vollzeit
Erforderliche Kompetenzen
Commissioning & Qualification (C&Q) Strategy & PlanningRisk Assessment (ISPE Baseline, ASTM E2500)Commissioning Execution (FAT, SAT, field commissioning)Qualification Protocol Authoring and Review (IQ/OQ/PQ)Requirements Traceability (URS to testing)Electronic Documentation Management and Data Integrity (ALCOA+)Change Control and CAPA ManagementVendor and Contractor Coordination during StartupCross-functional Collaboration and Stakeholder CommunicationTechnical Guidance, Mentoring, and Team LeadershipProcess Characterization Protocol Development and ExecutionValidation Summary Report PreparationMedical Device and Pharmaceutical Industry Regulatory Knowledge (GMP, FDA, EMA)Bilingual Spanish/English Communication
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