Supervisor, Transdermal - Night Shift

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.

Night Shift – 12-hour per day, rotating schedule (6:00pm-6:30am) 3 days on week 1 and 4 days on week 2 of pay cycle

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 Supervisor's 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.
• Operate and support complex process control systems utilizing advanced human-machine interfaces.
• 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.

Education:

• Bachelors Degree (BA/BS) Related field - Preferred
• Associate Degree Related field - Required

Experience:

• 5 years or more in Pharmaceuticals or manufacturing within a GMP environment
• 3 years or more in Leading and training staff

Specialized Knowledge:

• Transdermal, Converting, Packaging Experience with in a GMP Manufacturing Environment