GMP Validation Lead — CQV, CSV & Compliance

JobDiva, Inc.; Raleigh (NC); On-site; USD 110,000 - 160,000; Full time

Job summary

Creative Solutions Services, LLC seeks an experienced Senior Validation Specialist to lead qualification and validation activities in a GMP-regulated environment. You will plan, execute, review, and approve validation documentation for equipment, facilities, utilities, processes, and computerized systems while ensuring compliance with FDA, EMA, and cGMP regulations.

You will drive DQ/IQ/OQ/PQ, author validation plans and reports, manage deviations and CAPAs, and mentor junior staff.

Qualifications

• Bachelor's degree in Engineering, Life Sciences, Biotechnology, Pharmacy, Chemistry, or a related field.
• 5+ years of validation experience in a GMP-regulated environment.
• Strong knowledge of IQ/OQ/PQ, Process Validation, Equipment Qualification, Cleaning Validation, CSV, Risk Assessments, Change Control and CAPA.

Responsibilities

• Lead validation lifecycle activities including DQ, IQ, OQ, and PQ.
• Author, review, and approve validation protocols, reports, risk assessments, and validation plans.
• Execute equipment, process, cleaning, utility, facility, and computer system validation activities.
• Support commissioning and qualification activities for new equipment and manufacturing systems.
• Manage deviations, investigations, CAPAs, and change controls related to validation activities.
• Develop and maintain Validation Master Plans (VMPs).
• Ensure compliance with cGMP, FDA, EMA, GxP, and data integrity requirements.
• Support regulatory inspections and internal/external audits.
• Collaborate with Engineering, QA, Manufacturing, Automation, and Regulatory teams.
• Mentor junior validation engineers and specialists.

Skills

Validation experience

GxP compliance

Regulatory inspections

Leadership

Technical writing

Education

Bachelor's degree

Tools

CSV

Kneat

ValGenesis

MasterControl

TrackWise

Job description

Creative Solutions Services, LLC seeks an experienced Senior Validation Specialist to lead qualification and validation activities in a GMP-regulated environment. You will plan, execute, review, and approve validation documentation for equipment, facilities, utilities, processes, and computerized systems while ensuring compliance with FDA, EMA, and cGMP regulations.

You will drive DQ/IQ/OQ/PQ, author validation plans and reports, manage deviations and CAPAs, and mentor junior staff.