Life Sciences Validation Engineer — CQV, Travel‑Ready

PerkinElmer; Raleigh (NC); On-site; USD 68,000 - 121,000; Full time

Job summary

Project Farma, part of PerkinElmer, is seeking candidates who will reside within 50 miles of Raleigh, NC and be willing to travel domestically to meet client project requests. The role focuses on technical delivery across CQV, regulatory compliance, and project execution in life sciences projects.

The team collaborates to deliver high-quality project outcomes, develop professional skills, and uphold values of curiosity, personable, and patient-focused mindset.

Qualifications

• 1-7 years in consulting and/or engineering services.
• Willingness to travel domestically for client work.
• Residence within 50 miles of Raleigh, NC.

Responsibilities

• Execute specific technical tasks within a project, ensuring high-quality deliverables.
• Perform CQV tasks under guidance of Site Lead.
• Report technical issues and support resolution efforts.
• Ensure tasks meet regulatory requirements (FDA, GMP) and standards.
• Author technical documents (SOPs, specs, protocols, reports).
• Identify knowledge gaps and escalate as needed.
• Execute validation protocols using GxP best practices.
• Support billables as forecasted by site dashboards.

Skills

CQV tasks

Regulatory compliance

GxP knowledge

Project management

Communication

Education

Bachelor’s Degree in Life Science

Job description

Project Farma, part of PerkinElmer, is seeking candidates who will reside within 50 miles of Raleigh, NC and be willing to travel domestically to meet client project requests. The role focuses on technical delivery across CQV, regulatory compliance, and project execution in life sciences projects.

The team collaborates to deliver high-quality project outcomes, develop professional skills, and uphold values of curiosity, personable, and patient-focused mindset.