PharmEng Technology
About the job CQV Engineer
Job Title:
C&Q Engineer (Mid -Senior Level) Clean Utilities & Downstream Equipment Location:
Greater Raleigh Area, NC Industry:
Pharmaceutical Manufacturing Employment Type:
Full-Time or Contract
Position Summary:
We are looking for a
mid- to senior-level Commissioning & Qualification (C&Q) Engineer
to support project execution at a pharmaceutical manufacturing facility in the
Greater Raleigh area . This position is part of a project team focused on delivering commissioning and qualification activities for
clean utility systems
and
downstream process equipment .
This is a field-based, execution-oriented role. The ideal candidate will have hands-on experience with GMP systems, familiarity with clean utilities and downstream process equipment.
Key Responsibilities: Commissioning & Qualification: Support the preparation and execution of commissioning and qualification (IQ/OQ) protocols for clean utilities and downstream equipment. Perform P&ID walkdowns, loop checks, component verifications, and functional testing. Participate in FAT/SAT, equipment installation verification, punchlist tracking, and issue resolution. Assist with generating turnover packages (TOPs), traceability matrices, and related documentation. Collaborate with QA, automation, and construction teams to ensure systems are delivered per GMP and project standards. Document and escalate deviations and support resolution and closeout. Systems in Scope: Clean Utilities: Water for Injection (WFI) Clean steam Compressed air and process gases CIP/SIP systems Cleanroom HVAC systems Downstream Equipment:
Chromatography skids Tangential Flow Filtration (TFF) units Buffer prep and hold tanks Centrifuges Formulation vessels and associated skids Qualifications:
Bachelors degree in Engineering, Life Sciences, or related technical field. 5+ years of experience in C&Q within pharmaceutical or biotech GMP facilities. Proven experience with clean utility systems and downstream manufacturing equipment. Proficiency with
Kneat
for protocol development, execution, and documentation. Familiarity with P&IDs, engineering documentation, and protocol execution standards. Understanding of cGMP, ASTM E2500, and risk-based C&Q practices. Strong communication, organization, and technical writing skills. Collaborative mindset and ability to work effectively within cross-functional teams. Preferred Experience:
Project experience in greenfield or facility expansion projects. Exposure to DeltaV, SCADA, or building management/automation systems. Experience using commissioning tracking tools or turnover documentation systems.
Join our team
and play a critical role in supporting the startup and qualification of essential GMP systems for a leading pharmaceutical client in the
Greater Raleigh area . Opportunities are available for both
full-time
and
contract
roles.
Job Title:
C&Q Engineer (Mid -Senior Level) Clean Utilities & Downstream Equipment Location:
Greater Raleigh Area, NC Industry:
Pharmaceutical Manufacturing Employment Type:
Full-Time or Contract
Position Summary:
We are looking for a
mid- to senior-level Commissioning & Qualification (C&Q) Engineer
to support project execution at a pharmaceutical manufacturing facility in the
Greater Raleigh area . This position is part of a project team focused on delivering commissioning and qualification activities for
clean utility systems
and
downstream process equipment .
This is a field-based, execution-oriented role. The ideal candidate will have hands-on experience with GMP systems, familiarity with clean utilities and downstream process equipment.
Key Responsibilities: Commissioning & Qualification: Support the preparation and execution of commissioning and qualification (IQ/OQ) protocols for clean utilities and downstream equipment. Perform P&ID walkdowns, loop checks, component verifications, and functional testing. Participate in FAT/SAT, equipment installation verification, punchlist tracking, and issue resolution. Assist with generating turnover packages (TOPs), traceability matrices, and related documentation. Collaborate with QA, automation, and construction teams to ensure systems are delivered per GMP and project standards. Document and escalate deviations and support resolution and closeout. Systems in Scope: Clean Utilities: Water for Injection (WFI) Clean steam Compressed air and process gases CIP/SIP systems Cleanroom HVAC systems Downstream Equipment:
Chromatography skids Tangential Flow Filtration (TFF) units Buffer prep and hold tanks Centrifuges Formulation vessels and associated skids Qualifications:
Bachelors degree in Engineering, Life Sciences, or related technical field. 5+ years of experience in C&Q within pharmaceutical or biotech GMP facilities. Proven experience with clean utility systems and downstream manufacturing equipment. Proficiency with
Kneat
for protocol development, execution, and documentation. Familiarity with P&IDs, engineering documentation, and protocol execution standards. Understanding of cGMP, ASTM E2500, and risk-based C&Q practices. Strong communication, organization, and technical writing skills. Collaborative mindset and ability to work effectively within cross-functional teams. Preferred Experience:
Project experience in greenfield or facility expansion projects. Exposure to DeltaV, SCADA, or building management/automation systems. Experience using commissioning tracking tools or turnover documentation systems.
Join our team
and play a critical role in supporting the startup and qualification of essential GMP systems for a leading pharmaceutical client in the
Greater Raleigh area . Opportunities are available for both
full-time
and
contract
roles.