Validation Engineer I/II - Travel-Ready (Life Sciences)

Gamma Phi Omega International; Washington (District of Columbia); On-site; USD 58,000 - 71,000; Full time

Job summary

Project Farma seeks a Validation - Engineer I/II in Washington, DC area to support project execution with technical contribution and problem-solving. The role requires some travel to meet client project requests and adherence to FDA/GMP standards.

You will develop or execute validation protocols, write SOPs, and maintain strong collaboration with cross-functional teams. The successful candidate will have a life sciences or engineering background with 0–2 years of experience, and a commitment to

Qualifications

• Bachelor's Degree in Life Science, Engineering, or related discipline.
• 0-2 years in consulting and/or engineering services.
• Willingness to travel up to 100% or as required for client projects.
• Authorized to work in the United States without visa sponsorship.

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.

Skills

CQV tasks

Technical delivery

Education

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

Job description

Project Farma seeks a Validation - Engineer I/II in Washington, DC area to support project execution with technical contribution and problem-solving. The role requires some travel to meet client project requests and adherence to FDA/GMP standards.

You will develop or execute validation protocols, write SOPs, and maintain strong collaboration with cross-functional teams. The successful candidate will have a life sciences or engineering background with 0–2 years of experience, and a commitment to