The Manufacturing Associate 2 is an associate with a moderate level of technical expertise and experience. An MA2 may perform complex activities outside of routine manufacturing operations commensurate with their experience and training. An MA2 participates in the day to day operation of a cGMP compliant Manufacturing facility. Responsibilities include performing basic to complex activities related to operating bioprocess manufacturing equipment, completing the associated documentation of those activities, monitoring assigned processes using automated production systems and controls under limited supervision. Other activities include keeping the GMP manufacturing facility in a state of inspection readiness, using performance tools (Human Performance), and routine housekeeping activities. The MA2 must be technically capable with a good theoretical comprehension of general biopharmaceutical manufacturing equipment, principles and processes and have a good understanding of current GMP and safety standards and be able to apply this knowledge in a GMP manufacturing environment during performance of routine activities.