We are supporting a biotech client in South San Francisco that is seeking a Senior Validation & Facilities Engineer to step into an execution-heavy GMP environment and take ownership of facility and equipment qualification activities.
This is not a junior validation role and not a project management position . The client needs a hands-on senior engineer who can independently assess risk, define appropriate validation strategy, challenge vendor documentation when necessary, and execute qualification work with minimal oversight.
This is a great opportunity to truly own scope rather than operate under rigid templates!
Responsibilities
- Lead and execute facility and environmental qualification activities, including :
- Smoke studies / airflow visualization
- Pressurization and differential pressure studies
- Temperature mapping
- EMPQ support for GMP rooms
- Review and assess vendor commissioning and IOQ documentation for adequacy
- Determine when supplemental or wrapper protocols are required
- Support qualification of process and laboratory equipment (multiple units)
- Apply and justify representative qualification strategies where appropriate
- Perform P&ID walkdowns , redlines, and field verification
- Author and execute validation protocols and reports
- Coordinate with QA, Facilities, Engineering, Manufacturing, QC, and vendors
- Provide clear weekly progress updates and flag risks early
Requirements :
10+ years of hands-on validation and facilities engineering experience in a GMP biotech or pharmaceutical environmentProven experience leading validation execution , not just reviewing documentsStrong background in :Facility qualification and EMPQHVAC systemsSmoke studies / airflow visualizationTemperature mappingUtilities and process equipment qualificationComfortable making risk-based decisions and defending technical judgmentAble to work fully onsite in a fast-moving environment