Jobs · Quality Assurance · Colorado

Validation - Engineer II - Project Farma

PerkinElmer · Denver, CO · 1 mo ago
Quality Assurance$81k/yrFull-time

About the role

This is a full-time salaried position with Project Farma, a PerkinElmer company. The successful candidate will reside in the Colorado market and be willing to travel domestically to meet client project requests. Project Farma’s purpose is to improve patient lives by accelerating the delivery of life-changing therapies through the successful execution of high-quality life sciences projects across the full project lifecycle.

Team members collaborate with cross-functional teams to build trusted client relationships, deliver an exceptional customer experience, and contribute to business growth by identifying opportunities and applying data-driven insights to support project planning, cost, schedule, and performance management. All team members are expected to embody Project Farma’s values by being curious, personable, and unselfish, while maintaining a strong commitment to a Patient Focused and People First mindset.

Responsibilities

  • Technical Delivery
    • 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 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.
  • Talent Development
    • Focus on professional development and support team collaboration under the Site Lead's guidance.
    • Share technical knowledge with peers to support project delivery.
  • Business Growth & Development
    • 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 escalated properly.
    • Maintain professional relationships with project team members and client POCs at the operational level (e.g., technicians, engineers) to facilitate task completion.
  • Operational Performance & Billability
    • Maintain 100% individual billability by completing assigned project tasks.
    • Escalate any roadblocks to achieving billable targets to the site lead.

Requirements

  • 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).
  • 0-2 years of experience in consulting and/or engineering services.
  • Willingness to travel up to 100% or as required for client projects.
  • Must be authorized to work in the United States on a full-time basis; sponsorship is not available for this position.
  • Valid driver’s license required.

Pay

The annual compensation range for this full-time position is $74,500 - $81,000. The final base pay offered will be determined by factors including internal equity, work location, as well as individual qualifications, such as job-related skills, experience, and relevant education or training.

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