CSV Engineer - Bend, Oregon, USA

Advanced Manufacturing Tech Solutions

$90K — $110K *
Bend, OR 97701In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 3-5+ years in CQV/CSV in regulated industries
  • Bachelor's degree in Engineering, Life Sciences, Chemistry, Biology or related field preferred
  • Strong GMP / CQV / CSV background
  • Experience qualifying analytical laboratory instruments
  • Hands-on experience with equipment qualification
  • Familiarity with Kneat software strongly preferred
  • Excellent technical writing and documentation skills

Responsibilities

  • Support IQ/OQ/PQ for analytical instruments and GMP equipment
  • Develop and execute validation documentation and test scripts
  • Ensure compliance with CSV, data integrity, and GMP regulations
  • Collaborate with various teams including QC, QA, and Engineering
  • Manage deviations, CAPAs, and validation backlog activities
  • Utilize Kneat for validation documentation and workflows
  • Drive inspection-ready documentation and backlog remediation

Benefits

  • Support for professional development and training
  • Collaborative work environment with cross-functional teams
  • Opportunities to work in a fast-paced and impactful setting
  • Focus on high-priority qualification and validation activities
  • Engagement with cutting-edge technology and methodologies
Full Job Description
CSV Engineer - Bend, Oregon, USA AMTSOL is seeking a CSV/CQV Specialist to support high-priority qualification and validation activities within a cGMP environment. The role focuses on the qualification of analytical instruments, computerized systems and GMP equipment, and on driving inspection-ready validation documentation and backlog remediation. Key Responsibilities • Support IQ/OQ/PQ for analytical instruments, computerized systems and GMP equipment. • Develop and execute validation documentation, including URS, risk assessments, protocols, test scripts, traceability matrices and reports. • Support CSV, data integrity, 21 CFR Part 11, EU Annex 11 and GMP compliance. • Partner with QC, QA, Engineering, Automation, Instrumentation and system owners. • Manage deviations, CAPAs, change controls and validation backlog activities. • Use Kneat for validation documentation, workflows and approvals. • Help drive inspection-ready documentation and backlog remediation. Requirements • 3-5+ years' experience in CQV/CSV within pharmaceutical, biotech or regulated industries. • Bachelor's degree in Engineering, Life Sciences, Chemistry, Biology or a related field preferred. • Strong GMP / CQV / CSV background. • Analytical laboratory instrument qualification experience. • Hands-on equipment qualification experience. • Kneat experience strongly preferred. • Excellent technical writing and documentation skills. • Able to manage multiple priorities in a fast-paced environment.

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