Quay lại việc làm
ScovaiScovaiJobs
QRC Group, LLC

QRC Group, LLC

Sr Engineer

Juncos, PRTại chỗHợp đồngToàn thời gian

Đăng 23 thg 10, 2026

Công việc này được đăng bằng ES

We are seeking a Senior Engineer with hands-on experience with technical assessments supporting FDA/regulatory commitments, manufacturing-floor investigations, root cause analysis, deviation investigations, and CAPA development and implementation.

Key Responsibilities & Qualifications:


• Preparation, review, and approval of technical reports, engineering assessments, equipment evaluations, and technical justifications.

• Evaluation of equipment failures, performance issues, maintenance history, operating conditions, and potential impact to product, process, quality, and equipment qualified state.

• Technical support for deviations, investigations, CAPAs, change controls, risk assessments, and post-FDA commitments.

• Assessment of equipment design, functionality, reliability, lifecycle documentation, maintenance strategies, and continued fitness for intended use.

• Review and interpretation of engineering drawings, technical specifications, vendor documentation, equipment manuals, work orders, calibration records, and historical performance data.

• Development of clear, factual, and scientifically justified conclusions and recommendations based on available evidence.

• Experience collaborating with Manufacturing, Maintenance, Automation, Validation, Quality, Process Development, and external vendors to obtain and evaluate technical information.

• Knowledge of cGMP requirements and the ability to ensure that technical assessments are complete, traceable, inspection-ready, and supported by objective evidence.

• Strong technical writing, problem-solving, and communication skills, with the ability to independently manage multiple assessments and deliverables.

• Experience with purification, fermentation, process equipment, utilities, or pharmaceutical manufacturing systems is preferred.

• Strong field presence and willingness to inspect equipment and verify actual operating conditions within manufacturing areas.

Requirements

  • Bachelors in Engineering + 4 years of Engineering experience.
  • Bilingual (English & Spanish).
  • Technical Writing




Tóm tắt vai trò

Loại công việc

Toàn thời gian

Kỹ năng yêu cầu

FDA/Regulatory Technical AssessmentsRoot Cause AnalysisDeviation InvestigationsCAPA Development and ImplementationTechnical Report WritingEquipment Failure and Performance EvaluationEquipment Reliability and Lifecycle AssessmentEngineering Drawing and Technical Specification InterpretationcGMP Compliance and Inspection-Ready DocumentationRisk Assessment and Change ControlEvidence-Based Technical Problem-SolvingCross-Functional Technical CollaborationPharmaceutical Manufacturing Equipment and SystemsEnglish-Spanish Bilingual CommunicationManufacturing-Floor Equipment Inspection

Công việc tương tự

QG

Engineer

QRC Group

Juncos, PRTại chỗHợp đồngToàn thời gian
8 giờ trước
QG

Sr Associate EHS

QRC Group

Juncos, PRTại chỗHợp đồngToàn thời gian
8 giờ trước
QG

Sr Engineer

QRC Group

Juncos, PRTại chỗHợp đồngToàn thời gian
8 giờ trước
QRC Group, LLC

Process Development Senior Scientist

QRC Group, LLC

Juncos, PRTại chỗHợp đồngToàn thời gian
8 giờ trước
QG

Engineer

QRC Group

Juncos, PRTại chỗHợp đồngToàn thời gian
Hôm qua
IS

Specialist Manufacuring -35922 - Juncos, PR

Integrated Services For Productivity & Validation, Inc

Juncos, PRTại chỗHợp đồngToàn thời gian
Hôm kia