Early Career - CQV Engineer - Commissioning, Qualification & Validation
Full-time
PACIV
CQV Engineer (Commissioning, Qualification & Validation)
Location: Raleigh, NC (Hybrid)
Travel: Up to 40% Domestic and International Travel Bring Critical Manufacturing Systems to Life PACIV stands for Process Automation, Controls, Instrumentation & Validation. At PACIV, we help bring the future of advanced manufacturing to life by delivering world-class automation, validation, and instrumentation solutions. Our teams solve complex challenges, support industry-leading facilities, and make a measurable impact on critical manufacturing operations every day. We are looking for a CQV Engineer . In this position, you will support the commissioning, qualification, and validation of manufacturing systems, equipment, facilities, utilities, and automation systems within regulated pharmaceutical environments. You will work on high-impact capital projects that help transform complex systems into operational, compliant, and production-ready assets. PACIV does not provide H-1B sponsorship, H-1B transfers, OPT sponsorship or CPT sponsorship Responsibilities
PACIV offers a competitive compensation package designed to support employee well-being and long-term financial success.
#LI-DNI
Location: Raleigh, NC (Hybrid)
Travel: Up to 40% Domestic and International Travel Bring Critical Manufacturing Systems to Life PACIV stands for Process Automation, Controls, Instrumentation & Validation. At PACIV, we help bring the future of advanced manufacturing to life by delivering world-class automation, validation, and instrumentation solutions. Our teams solve complex challenges, support industry-leading facilities, and make a measurable impact on critical manufacturing operations every day. We are looking for a CQV Engineer . In this position, you will support the commissioning, qualification, and validation of manufacturing systems, equipment, facilities, utilities, and automation systems within regulated pharmaceutical environments. You will work on high-impact capital projects that help transform complex systems into operational, compliant, and production-ready assets. PACIV does not provide H-1B sponsorship, H-1B transfers, OPT sponsorship or CPT sponsorship Responsibilities
Develop and drive completion of Commissioning & Qualification (C&Q) deliverables, including validation plans, risk assessments, project strategies, user requirements, functional specifications, design specifications, impact assessments, traceability matrices, test cases, engineering studies, and final summary reports.
- Apply a strong understanding of commissioning and qualification principles to support project execution and regulatory compliance activities.
- Support pharmaceutical capital projects involving:
- A ctive pharmaceutical ingredient (API) manufacturing equipment
- Filling operations
- Device assembly systems
- Packaging equipment
- Facilities and utilities
- Automation systems
- Participate in project review meetings, including design reviews, qualification reviews, testing strategy discussions, execution reviews, and project status meetings.
- Develop, review, and maintain validation and qualification documentation within electronic lifecycle management systems.
- Assess, document, and support change management activities resulting from design updates, deviations, and testing outcomes.
- Participate in Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT) activities.
- Complete required client training and site-specific onboarding requirements.
- Perform other duties as assigned.
- Bachelor's degree in Biomedical or Chemical Engineering.
- Up to 3 years of experience with Commissioning & Qualification (C&Q) deliverables, CQV activities, validation documentation, or relevant academic/project experience.
- Strong understanding of validation principles and deliverables, including requirements development, design, testing, and reporting.
- Strong interpersonal, verbal, written, and presentation communication skills.
- Highly motivated, results-driven mindset with the ability to manage multiple priorities in a fast-paced environment.
- Demonstrated project management skills and the ability to independently drive assignments to completion.
- Ability to travel up to 40% domestically and internationally.
- Work on pharmaceutical manufacturing and life sciences capital projects.
- Gain hands-on experience with commissioning, qualification, validation, FAT, and SAT activities.
- Collaborate with experienced engineering, automation, and validation professionals.
- Build expertise working with manufacturing systems, utilities, facilities, and automation technologies.
- Contribute to projects that support critical manufacturing operations and production readiness.
PACIV offers a competitive compensation package designed to support employee well-being and long-term financial success.
- Generous Paid Time Off: Vacation, Sick Leave, and Company Holidays
- PACIV pays 90% of yearly health care premiums
- Health Savings Account (HSA) with Company Contributions
- 401(k) with Company Match up to 4% and immediate vesting with enrollment
- Full-time, direct-hire position
- No Corp-to-Corp (C2C) or 1099 arrangements
- PACIV does not partner with third-party recruiting agencies
- PACIV does not provide H-1B sponsorship, H-1B transfers, OPT sponsorship, CPT sponsorship, or employment-based immigration support.
#LI-DNI
Vacancy posted 4 days ago
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