VHP Isolator Validation Engineer

Verista, Inc.; Indianapolis (IN); On-site; USD 85,000 - 127,000; Full time

Benefits offered by this job

Competitive pay with incentive program

Company-paid life and disability ins.

Additional insurance options (supp. &/

Health Savings Account

Paid time off and holidays

Tuition reimbursement

Team social activities

Employee recognition program

Employee referral program

Parental leave and bereavement

Job summary

Verista is seeking a VHP validation specialist in Indianapolis, IN to lead cycle development and qualification for pharmaceutical isolators. The role emphasizes aseptic processing, BI placement, worst‑case strategies, and PQ protocol execution within a cGMP framework.

Ideal candidates bring strong technical writing, cross‑functional collaboration, and deep knowledge of regulatory expectations for VHP decontamination and barrier system lifecycle management.

Qualifications

• Hands-on experience with VHP cycle development and qualification for pharmaceutical isolators.
• Strong knowledge of aseptic processing and contamination control principles.
• Experience authoring and executing PQ protocols and final validation reports.
• Understanding GMP validation requirements in pharma/biotech manufacturing.
• Ability to troubleshoot VHP cycle development and performance issues.
• Excellent technical writing for protocols, reports, risk assessments, SOPs.
• Knowledge of regulatory expectations for VHP decontamination and lifecycle management.

Skills

VHP cycle development

BI placement strategies

PQ protocols

GMP validation

technical writing

regulatory knowledge

cross-functional collaboration

analyytical problem-solving

Education

Bachelor's in science/engineering

Job description

Verista is seeking a VHP validation specialist in Indianapolis, IN to lead cycle development and qualification for pharmaceutical isolators. The role emphasizes aseptic processing, BI placement, worst‑case strategies, and PQ protocol execution within a cGMP framework.

Ideal candidates bring strong technical writing, cross‑functional collaboration, and deep knowledge of regulatory expectations for VHP decontamination and barrier system lifecycle management.