INCOG BioPharma Services is seeking a Principal Validation Engineer to lead validation for sterile manufacturing systems, serialization, and computerized systems. You will partner with internal customers on client projects, facility upgrades, and lab systems, influencing outcomes without direct reporting authority.
The role requires deep CQV/CSV expertise, mentoring of engineers, and readiness to work onsite in a fast-paced manufacturing environment.
#J-18808-LjbffrSenior Validation Engineer – Sterile Systems & CSV Lead in fishers at Unknown Company
This position is listed as full time and onsite.