Payrate: $38.00 - $40.00/hr.

 

Summary:

Initial training will occur during the day shift. The ideal candidate will have significant experience in a GMP-regulated lab or manufacturing setting, with expertise in quality records management, including deviations and CAPAs. Proficiency with the Veeva Quality system is highly desirable.

 

Responsibilities:

• Execute QC second shift activities, collaborating with day and night shift team leads for tasks such as sample receipt, prioritization, and accurate entry into LIMS.


• Act as a point of contact for Manufacturing during night shift operations to support production schedules, resolve issues, and escalate risks.


• Perform routine and complex analytical testing in chemistry, bioassay, and/or microbiology, including STAT testing as needed.


• Ensure documentation is accurate and compliant with GDP, GMP, and ...