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

PerkinElmer

Los Angeles (CA)

On-site

USD 58,000 - 71,000

Full time

14 days+

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Job summary

PerkinElmer in the United States seeks an early-career Validation - Engineer I & II for Project Farma, supporting CQV tasks and technical delivery across multiple client sites. You will work under Site Leads to develop protocols, test equipment, and ensure compliance with FDA, GMP, and project requirements.

Based in markets such as Boulder, CO and other listed locations, this full-time role offers travel as needed, growth through hands-on experience, and collaboration with cross-functional teams

Qualifications

  • Bachelor's degree in Life Science, Engineering, or related discipline.
  • 0-2 years of consulting or engineering services experience.
  • Willingness to travel up to 100% 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 (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.
  • Maintain 100% individual billability by completing assigned project tasks.
  • Report workload or skill gaps within assigned tasks.

Education

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

Job description

PerkinElmer in the United States seeks an early-career Validation - Engineer I & II for Project Farma, supporting CQV tasks and technical delivery across multiple client sites. You will work under Site Leads to develop protocols, test equipment, and ensure compliance with FDA, GMP, and project requirements.

Based in markets such as Boulder, CO and other listed locations, this full-time role offers travel as needed, growth through hands-on experience, and collaboration with cross-functional teams

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