Validation Engineer I/II — Travel‑Heavy Life Sciences

Kappaalphapsi1911; Washington (District of Columbia); On-site; USD 58,000 - 71,000; Full time

Job summary

Project Farma, in Washington, DC, seeks an early-career Validation Engineer I/II to support project execution with technical contribution and problem-solving within defined scope. Travel up to 100% for client projects is expected, with emphasis on GMP compliance and high-quality deliverables.

You will perform CQV-related tasks, develop testing protocols, and author SOPs and requirement specifications under guidance, building foundational skills for growth in life sciences validation.

Qualifications

• Bachelor's degree in Life Science or Engineering or related field.
• 0-2 years in consulting/engineering services or equivalent.
• Willingness to travel up to 100% for client projects.

Responsibilities

• Execute specific technical tasks within a project.
• Perform CQV tasks or equipment testing under guidance.
• Report technical issues to Site Lead and support resolution.
• Ensure tasks meet FDA, GMP, and industry standards.
• Author technical documents such as SOPs and testing protocols.
• Maintain assigned billable targets as forecasted.

Skills

Willingness to travel

Education

Bachelor's degree in Life Science or Engineering

Job description

Project Farma, in Washington, DC, seeks an early-career Validation Engineer I/II to support project execution with technical contribution and problem-solving within defined scope. Travel up to 100% for client projects is expected, with emphasis on GMP compliance and high-quality deliverables.

You will perform CQV-related tasks, develop testing protocols, and author SOPs and requirement specifications under guidance, building foundational skills for growth in life sciences validation.