Onsite CSV/CQV Validation Specialist (6-9 Mo)

ASK Consulting; Bend (OR); On-site; USD 261,744,000 - 289,296,000; Part time

Job summary

ASK Consulting seeks a contractor-level CSV/CQV Specialist for a 6- to 9-month onsite engagement in Bend, OR. The role focuses on qualification and validation of analytical instruments, computerized systems, and GMP equipment, balancing CQV priorities with Instrumentation activities.

Ideal candidates have 3–5 years of CQV/CSV experience, hands-on lab qualification, and strong documentation skills to ensure regulatory compliance in a fast-paced, regulated environment.

Qualifications

• 3–5 years CQV/CSV in regulated environments.
• Experience validating analytical instruments and equipment.
• Familiar with cGMP, 21 CFR Part 11, and related standards.

Responsibilities

• Develop, execute, and maintain validation lifecycle documents.
• Support IQ/OQ/PQ activities and equipment qualification.
• Collaborate across CQV and Instrumentation teams and document thoroughly.
• Ensure data integrity and regulatory compliance in all activities.

Skills

CQV experience

CSV experience

GMP documentation

Multi-project management

Education

Bachelor’s degree in engineering or life sciences

Tools

Kneat validation

Job description

ASK Consulting seeks a contractor-level CSV/CQV Specialist for a 6- to 9-month onsite engagement in Bend, OR. The role focuses on qualification and validation of analytical instruments, computerized systems, and GMP equipment, balancing CQV priorities with Instrumentation activities.

Ideal candidates have 3–5 years of CQV/CSV experience, hands-on lab qualification, and strong documentation skills to ensure regulatory compliance in a fast-paced, regulated environment.