Biocon
Essential Duties and Responsibilities include the following.
Other duties may be assigned.
Is this your next job Read the full description below to find out, and do not hesitate to make an application.
Assist Production Management with all scheduled and requested activities in an efficient and smooth operation. Ensure all scheduled commercial and non-commercial manufacturing activities are completed on time. Become proficient in the setup, operation, and cleaning of all cGMP equipment used during production operations and to supervise individuals performing these actions. Participate in all Quality Investigations as required. Be able to provide written support as required. Adhere to all approved Standard Operating Procedures, Batch Records, and Safety Procedures as written when performing all daily activities. Ensure the cGMP area is cleaned and maintained following all SOPs and good housekeeping practices. Must use required PPE during cGMP activities as specified in the Batch Records and Safety Data Sheets.
Education and / or Experience:
High School Diploma or GED Equivalent with 10-15 years related experience in cGMP production operation activities and limited supervisor experience or bachelor's degree in physical sciences or pharmaceutical life-science related field of study. Familiarity with working and supervising operators in a regulated pharmaceutical solid dosage facility. Ability to read and write documents written in English. Able to work with minimal supervision. Maintain personal hygiene habits consistent with working in a cGMP environment. Be capable of wearing all required PPE; including partial and full facepieces based on OSHA guidelines.
Must have Valid work permit.
Other duties may be assigned.
Is this your next job Read the full description below to find out, and do not hesitate to make an application.
Assist Production Management with all scheduled and requested activities in an efficient and smooth operation. Ensure all scheduled commercial and non-commercial manufacturing activities are completed on time. Become proficient in the setup, operation, and cleaning of all cGMP equipment used during production operations and to supervise individuals performing these actions. Participate in all Quality Investigations as required. Be able to provide written support as required. Adhere to all approved Standard Operating Procedures, Batch Records, and Safety Procedures as written when performing all daily activities. Ensure the cGMP area is cleaned and maintained following all SOPs and good housekeeping practices. Must use required PPE during cGMP activities as specified in the Batch Records and Safety Data Sheets.
Education and / or Experience:
High School Diploma or GED Equivalent with 10-15 years related experience in cGMP production operation activities and limited supervisor experience or bachelor's degree in physical sciences or pharmaceutical life-science related field of study. Familiarity with working and supervising operators in a regulated pharmaceutical solid dosage facility. Ability to read and write documents written in English. Able to work with minimal supervision. Maintain personal hygiene habits consistent with working in a cGMP environment. Be capable of wearing all required PPE; including partial and full facepieces based on OSHA guidelines.
Must have Valid work permit.