POSITION SUMMARY: ·       This position is responsible for performing manufacturing procedures and the execution of scheduled tasks within a CGMP environment in Downstream Manufacturing. This position is responsible for quality and maintaining the highest standards in compliance within company policies, procedures and all applicable regulations.  EDUCATION and/or EXPERIENCE: ·       College degree or an equivalent combination of education and experience ·       Biotech/Pharmaceutical industry experience preferred or relevant experience working with Standard Operating Procedures (SOP’s) where formal documentation is required ·       Previous experience with MES would be an advantage ·       Knowledge of routine and non-routine testing and sampling methods, techniques and related equipment would be an advantage