Biocon
Essential Duties and Responsibilities include the following. Other duties may be assigned.
- 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.