Supervisor, Transdermal

Amneal India•Piscataway, NJ

21d

About The Position

The Supervisor will oversee the operations and staff throughout the manufacturing floor. The supervisor will also assist with equipment start-up, participate in ANDA batch production and commercial batch manufacturing. This role follows a 12-hour rotating schedule, working from 6:00 AM to 6:30 PM. Essential Functions: Oversee all activities throughout the manufacturing floor. Ensure safety, quality, and effective productivity, adhering to 100% GMP compliance. Plan and schedule all manufacturing and packaging activities to ensure deadlines are met, prevent a back order situation. Work closely with the quality group to ensure constant compliance, participate in any and all investigations that may arise in the department. Support the R&D process and execution of new products is expected, will be a key contributor of information during the process. Act as a "Working Supervisor" to manufacture the various R&D large/small scale batches, train operators in the processing and equipment capabilities for all production. Participate in equipment set-up, IQ/OQ/PQ, and commercial batch activities. Set-up, run and clean equipment in a GMP compliant environment. Conduct mixing, coating, converting, pouching and cartoning operations. The Working Supervisor responsibility is a key aspect of the role as it pertains to leading, performing and demonstrating the actual methods and procedures in manufacturing the products using state-of-the-art equipment and operating systems. These systems include sophisticated recipe driven controlled human interface systems. Conduct effective communication to the staff on a daily basis to ensure that everyone is up to speed with the all pertinent departmental and/or company events. Additional Responsibilities: R&D and commercial scale-up activities. Perform Continuous Improvements.

Responsibilities

Oversee all activities throughout the manufacturing floor.
Ensure safety, quality, and effective productivity, adhering to 100% GMP compliance.
Plan and schedule all manufacturing and packaging activities to ensure deadlines are met, prevent a back order situation.
Work closely with the quality group to ensure constant compliance, participate in any and all investigations that may arise in the department.
Support the R&D process and execution of new products is expected, will be a key contributor of information during the process.
Act as a "Working Supervisor" to manufacture the various R&D large/small scale batches, train operators in the processing and equipment capabilities for all production.
Participate in equipment set-up, IQ/OQ/PQ, and commercial batch activities.
Set-up, run and clean equipment in a GMP compliant environment.
Conduct mixing, coating, converting, pouching and cartoning operations.
Conduct effective communication to the staff on a daily basis to ensure that everyone is up to speed with the all pertinent departmental and/or company events.
R&D and commercial scale-up activities.
Perform Continuous Improvements.