-Prior experience in small- to intermediate-scale cell therapy manufacturing under GMP conditions strongly preferred.
- Familiarity with autologous cell therapy manufacturing workflows is highly desirable.
-Experience with aseptic technique in ISO-classified cleanroom environments.
-Working knowledge of cGMP regulations and documentation practices.
-Understanding of Quality Control processes and basic analytical testing methods.--Experience with flow cytometry, cell counting systems, or other cell-based analytical assays is a plus.
-Prior hands-on experience in clinical-stage cell therapy manufacturing under GMP conditions.
-A working understanding of quality control principles, and basic analytical testing skills to support in-process monitoring and product release activities.

Skills:
-Strong aseptic technique.
-High attention to detail and documentation accuracy.
-Ability to follow complex written procedures precisely.
-Understanding of chain-of-identity and chain-of-custody principles-Team-oriented with strong communication skills.
-Ability to work in a fast-paced clinical manufacturing environment.
-Proficient in Office Suite software.

PHYSICAL QUALIFICATIONS:
-Must be able to lift heavy boxes (approximately 50 lbs)
-Must be in good physical condition to clean the GMP facilities on a regular basis

For consideration, please complete an application and include a cover letter, resume and the names and email addresses of three to five references. 

 Application must be submitted by 11:55 p.m. (ET) of the posting end date.