Validation Engineer I/II – Travel‑Ready Life Sciences

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

Job summary

Project Farma in the United States seeks an early-career Validation Engineer I & II to support project execution across life sciences projects. You will perform CQV tasks, develop protocols, and ensure compliance with FDA and GMP standards while reporting to the Site Lead.

With 0–2 years of experience, you will build foundational skills, contribute to billable tasks, travel as required, and collaborate with cross-functional teams to deliver high-quality results in a fast-paced environment.

Qualifications

• Bachelor's Degree in Life Science, Engineering, or related discipline (OR a combination of equivalent work experience in capital project engineering, pharma cGMP facility start-up, CapEx/OpEx project management and/or comparable military experience).
• Years of Experience: 0-2 years in consulting and/or engineering services.
• Willingness to travel up to 100% or as required for client projects.

Responsibilities

• Execute specific technical tasks within a project, ensuring high-quality deliverables.
• Perform CQV tasks, such as protocol development or equipment testing, under the Site Lead's guidance.
• Report technical issues to the Site Lead and support resolution efforts.
• Ensure tasks meet client specifications, regulatory requirements (e.g., FDA, GMP), and industry standards.
• Author technical documents: SOPs, requirements specifications, testing protocols, summary reports, etc.
• Identify and close individual knowledge gaps with support from other team members or leads as needed.
• Execute system and process validation protocols by using GxP best practices.
• Ensure billable targets are met each month as forecasted by respective site dashboards.
• Report workload or skill gaps within assigned tasks.
• Focus on professional development and support team collaboration under the Site Leads guidance.
• Share technical knowledge with peers to support project delivery.
• Contribute to project-level success by delivering high-quality work that supports business growth opportunities.
• Build meaningful internal and external relationships.
• Present Project Farma as a service to clients as needed.
• Communicate with clients in a professional manner.
• Ensure any client feedback or opportunities identified are being escalated properly.
• Maintain professional relationships with project team members and client POCs at the operational level (e.g., technicians, engineers) to facilitate task completion

Education

Bachelor's Degree in Life Science, Engineering, or related discipline

Job description

Project Farma in the United States seeks an early-career Validation Engineer I & II to support project execution across life sciences projects. You will perform CQV tasks, develop protocols, and ensure compliance with FDA and GMP standards while reporting to the Site Lead.

With 0–2 years of experience, you will build foundational skills, contribute to billable tasks, travel as required, and collaborate with cross-functional teams to deliver high-quality results in a fast-paced environment.