Assist with supervising employees to ensure compliance of cGMP during complete operation of compression. Ensure process flow is meeting the required levels.
Essential Functions
Plan and execute compression operation as per monthly planning. Control and maintain tracking of batch records. Review batch record and provide to next department on time. Inform management if there is an observation of wrong doing during the manufacturing process.
Review and verify all compression operators use log book for correct data entry.
Train compression operators on safety parameters during operation of compression.
Prevent Mix up, Cross Contamination during compression.
Communicate to engineering department on Dust Collector clean up.
Monitor room temperature and humidity on environmentally sensitive products. Maintain In-process Check Control during compression process.
Must follow up on Amneal Compression CAPA.
Check Calibration status of all scale, balance, and equipment (Routine)
Additional Responsibilities
Others duties as assigned.
Education
High School or GED in General HS - Required
Work Experience
7 years or more in Pharmaceutical/Manufacturing Environment - Required
Skills and Abilities
Good communication written and verbal. - Intermediate
Good supervising a group of employees. - Intermediate
Ability to read, write, and communicate in English at a level to facilitate the understanding terminology of the job. - Intermediate
Ability to comprehend and follow written and verbal procedures or instructions - Intermediate
Have basic math and mechanical skills - Intermediate