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Job description
CQV Engineer - Pharmaceutical Manufacturing
Location: Clayton, North Carolina
Contract: 24 months, with potential for extension
Pay Rate: $65/hour
Work Model: On-site
We are seeking an experienced CQV Engineer to support commissioning, qualification, and validation activities across pharmaceutical manufacturing projects in Clayton, NC.
The CQV Engineer will lead validation efforts for assigned projects from requirements definition through qualification, validation, change control, and decommissioning. Projects may involve facility systems, aseptic formulation and filling, medical device assembly, packaging, warehouse and QC operations, manufacturing systems, and computerized equipment.
This position requires previous pharmaceutical validation experience and the ability to independently develop and execute validation deliverables following an initial onboarding period.
Key Responsibilities
Lead commissioning, qualification, and validation activities for assigned pharmaceutical manufacturing projects.
Develop, revise, and maintain validation plans, reports, specifications, risk assessments, traceability matrices, and decommissioning documentation.
Author and execute Design Qualification/Review, Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and Process Validation protocols and reports.
Support commissioning and qualification activities to ensure equipment and systems are ready for validation execution.
Participate in Factory Acceptance Testing (FAT) where required.
Track validation documentation, milestones, risks, and deliverables across multiple concurrent projects.
Provide regular project status updates and escalations to Project Managers.
Identify, investigate, and document deviations and engineering changes encountered during validation.
Initiate, author, and support Change Controls and assess the validation impact of proposed changes.
Participate in recurring project meetings and lead focused validation meetings when required.
Use electronic validation and quality systems such as TIMS/HP ALM and Veeva QualityDocs/Vault Quality.
Ensure validation activities comply with GMP, FDA requirements, EU Annex 15, GAMP 5, and applicable company procedures.
Support project activities during plant shutdowns, which may occasionally require evening or weekend work.
Preferred Experience
Candidates with pharmaceutical validation experience in one or more of the following areas are particularly relevant:
Manufacturing equipment upgrades and production line modifications
Aseptic formulation and filling equipment, including RABS
Vision inspection systems
Medical device assembly equipment
Pharmaceutical packaging equipment
Process control and manufacturing execution systems, including SCADA, PLC, PAS-X, and LMES
Laboratory and GMP facility modifications
Process instrumentation, monitoring, and calibration systems
BMS, HVAC, refrigeration, and facility utility systems
Electrical distribution, switchgear, and controls
Physical security, access control, and CCTV systems
Technology modernization and lifecycle replacement projects
Electronic validation documentation and execution
Qualifications
Demonstrated experience generating and executing validation documentation within a pharmaceutical or regulated GMP manufacturing environment.
Hands-on experience with commissioning, qualification, and validation activities.
Strong knowledge of IQ/OQ/PQ, risk assessments, traceability, deviations, and change control.
Understanding of applicable GMP, FDA, EU Annex 15, and GAMP 5 requirements.
Ability to independently manage validation deliverables across multiple projects after onboarding.
Strong technical documentation, communication, and project coordination skills.
Ability to work on-site in Clayton, North Carolina.
Flexibility to support occasional evening or weekend activities during major project execution or plant shutdowns.
This is an excellent opportunity for an experienced CQV or Validation Engineer to join a long-term pharmaceutical manufacturing program and work across a diverse portfolio of equipment, facility, automation, and manufacturing projects.
Desired Skills and Experience
Commissioning & Qualification (CQV), Validation, GMP, Equipment Qualification, IQ/OQ/PQ, Process Validation, FDA Regulations, EU Annex 15, GAMP 5, Veeva Vault, Change Control, Deviation Management, Aseptic Processing, Pharmaceutical Manufacturing
Worksite address
township of clayton, NC, 27520, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.