About Client:


Client is the global contract development and manufacturing services platform of large chemical therapeutics company which is a leading external development and manufacturing partner that focuses exclusively on the cell therapy industry. Client is investing a ton of money into the organization. The company is growing fast with 6 clean rooms scheduled to be up and ready within the next 12 months. 

About this Group:

This is in the Q/A team. 4 total managers of this group and roughly 30 members of the team. This is a Mon-Fri 1st shift role, but candidates need to be able to work weekends


Must-Have:

  1. 2 years Validating Manufacturing equipment and QC equipment
  2. Pharmaceutical industry experience is a must-have. Cell therapy manufacturing preferred).


ADDITIONAL COMMENTS:

  1. The client will NOT consider consultants who have been working on 1-2 year contracts assignment.
  2. This is a full-time direct-hire position, so candidates who have been working as contractors will not be considered. 

QA VALIDATION ENGINEER - COMPLIANCE, ALLENDALE, NJ - ID RF08A

QA VALIDATION ENGINEER - COMPLIANCE

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