Senior CSV​/Lab Instrument Validation Consultant

Sr. CSV / Lab Instrument Validation Specialist

Type of role:
Contract

Duration: 12-36+ months

Hourly pay rate: DOE (C2C, W2, or 1099 permissible)

Location:

South San Francisco Bay Area (Remote during COVID)

Our customer is seeking a Senior CSV / Lab Instrument Validation Engineer who is well versed in laboratory Instrument processes within a Pharmaceutical environment. Must have hands experience on Lab Instrument Qualification. You will be primarily responsible for planning, leading, and executing validation efforts for standalone Lab Instrument Software systems.

Must have strong experience in the following:

• Responsible for performing validation of Laboratory Instrumentation by following approved standard operating procedures (SOPs), current Good Manufacturing Practices (GMPs) and all other regulatory requirements.
• Responsible for the mapping and bringing consistency to the instrument lifecycle globally, from supporting purchase to instrument validation to decommissioning documentation.
• Plan, lead, and execute the standardizing of validation efforts for standalone Lab Instrument Software systems.
• Responsible for developing and executing on validation plans according to approved procedures, collation of test results, and organizes data packages and maintains all documentation pertaining to validation.
• Ability to compile and analyze validation data, prepare reports and makes recommendations for changes and/or improvements.
• Well versed in Laboratory Instrument process, ability to provide guidance to management on what improvements need to be made. (Essential for this role)
• May also investigate and trouble-shoot problems which occur, and determine solutions.
• Support change management and manage existing lab systems.
• Participates on cross-functional project teams with the support of Development, Quality, and other groups
• Familiar with FDA guidelines for Instrument and Software validation.
• Experience must come from a pharmaceutical, biotech industry with direct knowledge of FDA regulations including 21
  
  CFR Part 11.
• Self-motivated, good communication, technical writing, presentation skills, detail oriented, analytical, and a team player.