Validation Engineer II

Job Title:
Validation Engineer II

Location:

Oregon
Work Arrangement:
Onsite

Contract:

6 9 Months

Employment Type:

W2

We are seeking a Validation Engineer to join a pharmaceutical project in Bend, OR, supporting ongoing qualification and compliance activities across laboratory and GMP systems.

This position is well suited for someone with a combination of CQV and CSV experience who has worked directly with analytical laboratory instruments. The engineer will collaborate with CQV and Instrumentation teams to complete equipment and system qualification activities, address a current validation workload, and maintain accurate GMP documentation.

• 3 5 years of validation experience in pharmaceutical, biotech, or a similar regulated environment
• Practical experience qualifying analytical laboratory instruments and GMP equipment
• Exposure to both CQV and Computerized Systems Validation (CSV)
• Good understanding of cGMP requirements and validation documentation practices
• Ability to independently manage several qualification activities and changing priorities
• Experience supporting large validation workloads or remediation initiatives is beneficial
• Bachelor's degree in Engineering, Chemistry, Biology, Life Sciences, or a related discipline preferred

Candidates with strong analytical laboratory experience combined with both CSV and CQV knowledge will be given preference.