Senior CSV / Lab Instrument Validation Consultant
Company: AdeptSource
Location: Belmont
Posted on: April 2, 2026
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Job Description:
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 21CFR Part 11.
Self-motivated, good communication, technical writing, presentation
skills, detail oriented, analytical, and a team player. Dawn West
AdeptSource
Keywords: AdeptSource, Tracy , Senior CSV / Lab Instrument Validation Consultant, Science, Research & Development , Belmont, California
