Lab Instrument Qualification / Validation Consultant from Adept Source
Redwood City, CA
About the Job
Title: Lab Instrument Qualification / Validation Consultant
Type of role: Remote Contract
Duration: 3+ Months
Customer Location: Redwood City, CA - Remote role
Our customer is seeking a Lab Instrument Qualification / 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:
Type of role: Remote Contract
Duration: 3+ Months
Customer Location: Redwood City, CA - Remote role
Our customer is seeking a Lab Instrument Qualification / 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.
- 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.