Pharma Validation Engineer — On-Site, Growth & Compliance

Vpicompounding

Centennial (CO)

On-site

USD 48,000 - 55,000

Full time

14 days+

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Benefits offered by this job

Company-paid health, dental, andVision
401(k) plan with employer match
6 paid company holidays per year
32 hours of PAID floating holiday time
Paid Time Off (PTO) accrual
Tuition and certification reimburse
RTD EcoPass for public transportation
Career growth opportunities with hands
On-site training and advancement

Job summary

VPI Compounding Pharmacy seeks a Validation Engineer to support pharmaceutical manufacturing operations in Centennial, CO. This full-time role emphasizes hands-on work, cGMP compliance, and developing and maintaining validation documentation throughout the lifecycle.

The ideal candidate will coordinate equipment and process qualifications, assist with cleanroom certifications, and liaise with vendors to ensure regulatory standards are met.

Qualifications

  • Understanding of scientific and mathematical principles.
  • Strong verbal and written communication skills.
  • Ability to read and follow SOPs, cGMPs, and regulatory guidelines.

Responsibilities

  • Develop, write, and maintain validation protocols, reports, and SOPs in compliance with FDA, USP, and cGMP requirements.
  • Coordinate and execute equipment and process qualifications.
  • Maintain full documentation throughout the validation lifecycle.
  • Support cleanroom certification and recertification every six months.

Skills

Scientific principles
Verbal and written communication
Regulatory guidelines interpretation

Education

Bachelor’s degree in Engineering (Chemical, Mechanical, Manufacturing, Electrical, or Software)

Tools

Microsoft Word
Microsoft Excel

Job description

VPI Compounding Pharmacy seeks a Validation Engineer to support pharmaceutical manufacturing operations in Centennial, CO. This full-time role emphasizes hands-on work, cGMP compliance, and developing and maintaining validation documentation throughout the lifecycle.

The ideal candidate will coordinate equipment and process qualifications, assist with cleanroom certifications, and liaise with vendors to ensure regulatory standards are met.

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