Supervisor, Transdermal - Night Shift
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At a glance
Job overview
Amneal Pharmaceuticals is hiring a Supervisor, Transdermal - Night Shift. The Supervisor, Transdermal will oversee manufacturing operations and staff, ensuring safety, quality, and productivity while adhering to GMP compliance. This role involves assisting with equipment start-up, participating in ANDA batch production, and commercial batch manufacturing. The supervisor will also support R&D processes and continuous improvements.
Key focus areas include Oversee all activities throughout the manufacturing floor, Ensure safety, quality, and effective productivity, and Adhere to 100% GMP compliance.
Important skills include GMP Compliance, Planning And Scheduling, QA, Investigations, R&D Process Support, and Training Operators.
Skills & qualifications
Skills
Full job description
Description:
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 PM to 6:30 AM. (Requires every other weekend)
Essential Functions:
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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.
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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.
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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.
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Actively perfrom and demonstrate manufacturing processes while supervising daily operations
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Participate in equipment set-up, IQ/OQ/PQ, and commercial batch activities. Set-up, run and clean equipment in a GMP compliant environment.
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Conduct mixing, coating, converting, pouching and cartoning operations.
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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:
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R&D and commercial scale-up activities.
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Perform Continuous Improvements.
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