Validation Engineer

Description

The Validation Engineer will support commissioning, qualification, process validation, cleaning validation, and validation lifecycle activities at the Phlow Petersburg Campus. This role requires a flexible, hands‑on validation professional and can author and execute protocols, support field activities, resolve deviations, evaluate data, and complete final reports.

• Support validation projects from planning through execution, final reporting, and closeout activities.
• Author, review, and execute validation documentation including URS, risk assessments, FAT, SAT, IQ, OQ, PQ, traceability matrices, and summary reports.
• Assist in development and revision of SOPs, Validation Master Plans (VMPs), work instructions, and quality system documentation.
• Maintain accurate and complete validation records in accordance with document control and data integrity requirements.
• Participate in project planning, scheduling, and resource coordination to ensure validation deliverables are completed on time.

• Support qualification and validation of manufacturing equipment, process systems, utilities, clean rooms, facilities, laboratory instruments, automation systems, and cleaning processes.
• Perform equipment walkdowns, commissioning support, startup activities, requalification, periodic reviews, and lifecycle management activities.
• Review technical drawings, P&IDs, specifications, calibration records, maintenance records, and vendor documentation to support qualification activities.
• Support technology transfers, facility expansions, equipment upgrades, and remediation projects.

• Support process validation protocol execution, continued process verification (CPV), and process performance monitoring.
• Collect, analyze, and trend validation data to ensure compliance with approved acceptance criteria and regulatory requirements.
• Assist with new product introductions and validation activities associated with process changes and improvements.

• Assist with cleaning validation strategies, master plans, protocols, sampling plans, execution activities, and final reports.
• Support surface area calculations, worst‑case product selection, swab and rinse sampling, recovery studies, hold‑time studies, residue limit calculations, and CIP, COP, and manual cleaning validation activities.
• Evaluate and document cleaning effectiveness to ensure product quality and regulatory compliance.

• Document, investigate, and support resolution of deviations, CAPAs, investigations, nonconformances, and change controls.
• Ensure compliance with cGMP, FDA, EMA, ICH, ISPE, and company quality standards.
• Support internal audits, client audits, regulatory inspections, and responses to audit observations.
• Participate in continuous improvement initiatives focused on compliance, quality, efficiency, and inspection readiness.

• Coordinate validation activities with Engineering, Manufacturing, MS&T, QA, QC, Maintenance, Facilities, Automation, and external vendors.
• Provide technical support and training to internal teams regarding validation requirements, documentation practices, and regulatory expectations.
• Facilitate consultant‑to‑internal staff knowledge transfer to ensure long‑term sustainability of validation programs and processes.
• Collaborate with cross‑functional stakeholders to identify and resolve technical and compliance issues throughout the validation lifecycle.

The salary range for this position is $90,000 to $115,000, with the final offer determined based on factors such as the candidate's experience, qualifications, skills, and education. In addition to a competitive base salary, this position is eligible to participate in Phlow's bonus and stock option programs. Phlow also offers a comprehensive benefits package that includes medical, life, and disability insurance;

retirement savings plans; paid time off and company holidays; and education-related benefits. Many of these programs are fully funded or significantly subsidized by the company, reflecting our commitment to…