Validation Engineer I/ II

Work Location or Remote
On-site
Remote?
No
Full time or part time?
Full time
Shift
Hours
40/week
Number of Positions
1
Any possibility of the assignment to be converted to a full-time role?
Not at this time
Duties
Perform Smoke studies and assist in semi annual Media fill qualifications as a SME
Perform requalification/periodic review of autoclaves, depyrogenation tunnels, cold rooms, freezers and warehouse areas.
Has worked with Ellabs data loggers and software
Write and execute protocols and complete final reports.
Understanding of cleaning validation concepts and principles.
Understands pharma grade utilities ( water HVAC, gases)
Support Maintenance, Engineering and Production Depts. in the selection, review, acquisition, and upgrade of systems and production equipment.
Provide technical support in developing user and functional requirements specifications, URS, RA, FRS, and DQ for systems and equipment.
Develops and Assists with audit responses and completion of assigned CAPAs by target due dates. Included is the responsibility for making sure Validation areas are "inspection ready" at all times.
Support Change Control, Deviation and CAPA activities

Skills
Aseptic processing
Protocol generation
Sterilization
Validation
FDA/USDA

Bachelors , preferable in a science or engineering related field