The Role
Support process engineering for pharmaceutical manufacturing recapitalization, BCP, equipment lifecycle, capital projects, commissioning/qualification, validations, CAPA, investigations, and continuous improvement while ensuring quality, safety, and environmental compliance.
Summary Generated by Built In
Process Engineering to provides technical and project execution support for recapitalization initiatives, Business Continuity Planning (BCP) efforts, and general process engineering activities within a regulated pharmaceutical manufacturing environment.
This role supports equipment lifecycle management, capital project execution, process improvements, asset delivery activities, technical investigations, and continuous improvement initiatives while ensuring compliance with quality, safety, and environmental standards.
Skills:
- Capital Projects & Equipment Lifecycle Management
- Commissioning & Qualification
- CAPA
- Investigations
- Validation Cycle
Requirements
- Bachelor's in Engineering
- Bilingual (Spanish/English)
- Technical Writing
- Ability to manage multiple projects and priorities simultaneously
- Capital Projects and Equipment Installation
Skills Required
- Bachelor's in Engineering
- Bilingual (Spanish/English)
- Technical writing
- Ability to manage multiple projects and priorities simultaneously
- Capital projects and equipment installation
- Capital projects & equipment lifecycle management
- Commissioning & qualification
- CAPA
- Investigations
- Validation cycle
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The Company
What We Do
QRC Group specializes in providing expert consulting services in regulatory compliance, quality management, and risk management for the pharmaceuticals, medical devices, biotechnology, and other regulated industries, delivering comprehensive project management and validation solutions.
