More jobs:
CQV Associate : Commissioning, Validation & Quality
Job Description & How to Apply Below
A global CDMO specializing in cell and gene therapies is seeking an Associate I for Commissioning, Qualification, and Validation in Hamilton, Ontario. The candidate will focus on validating equipment, maintaining schedules, and collaborating with various departments to ensure compliance with GMP standards. Applicants should have at least a year of experience in CQV roles and strong technical writing abilities. This is a 6-month contract role, ideal for those looking to deepen their expertise in the biopharma sector.
#J-18808-Ljbffr
Position Requirements
10+ Years
work experience
Note that applications are not being accepted from your jurisdiction for this job currently via this jobsite. Candidate preferences are the decision of the Employer or Recruiting Agent, and are controlled by them alone.
To Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search:
To Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search:
Search for further Jobs Here:
×