Validation Engineer — CQV for Pharma, with ESOP & PTO

CAI; Raleigh (NC); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Comprehensive Health Insurance

24 days of Paid Time Off

15% Company Contribution to ESOP/401K

Company paid Life Insurance

Company paid Long Term Disability

Job summary

A leading professional services company located in North Carolina seeks candidates for a CVQ role focused on commissioning and qualification within regulated industries. Responsibilities include developing technical documentation, executing protocols, and managing project work. Candidates should hold a bachelor's degree in a science or engineering field and possess 2-4 years of relevant experience. The position offers comprehensive health benefits, paid time off, and a strong dedication to diversity and inclusion.

Qualifications

• 2-4 years’ experience in a regulated industry.
• Familiar with pharmaceutical facilities and utilities.
• Experience in facilities and equipment startup is preferred.

Responsibilities

• Develop documentation for CQV activities.
• Write and execute protocols for field verification.
• Plan and coordinate work, direct small teams.

Skills

Commissioning and qualification

Technical documentation

Project management

Troubleshooting

Education

Bachelor’s degree in science or engineering

Tools

ISPE Baseline Guide 5

Pharmaceutical manufacturing processes

Job description

A leading professional services company located in North Carolina seeks candidates for a CVQ role focused on commissioning and qualification within regulated industries. Responsibilities include developing technical documentation, executing protocols, and managing project work. Candidates should hold a bachelor's degree in a science or engineering field and possess 2-4 years of relevant experience. The position offers comprehensive health benefits, paid time off, and a strong dedication to diversity and inclusion.