LEAD3R is looking to speak with Manufacturing Science & Technology Engineers to join our client at their facility in the greater Salt Lake City, Utah area.

Main Responsibilities, not exhaustive:

• Author and execute equipment commissioning and qualification documents.
• Author SOPs, batch records and generate engineering drawings, reports and specifications.
• Serve as a technical expert to receive the technology transfer from Development to cGMP manufacturing.
• Manage production runs and events in cGMP manufacturing environment.

Required Qualifications:

• Minimum of a BS/BA and minimum 5+ years of experience in cGMP manufacturing environment.
• Must have direct experience with upstream and downstream processes using aseptic processing techniques in a cleanroom environment.
• Experience with biologics.

If you or someone you know may be interested, please send your resume to Allison.Sudman@LEAD3R.COM or visit Lead3r.com to learn more about us. #LifeSciences #LEAD3Rjobs #LEAD3R