Supervisor, Transdermal - 3rd Shift (12 Hours) at Amneal Pharmaceuticals LLC (J0P) in Piscataway, New Jersey

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.

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.

Education:

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


• Associate Degree Related field + 5 yrs exp leading and training staff - Required

Experience:

• 3 years or more in Transdermal drug delivery or manufacturing GMP environment


• 3 years or more in Leading and training staff

Skills:

• Strong analytical and quantitative skills with good common sense. - Intermediate


• Excellent oral and written communication skills. - Intermediate


• Able to multi-task, and advance multiple programs simultaneously. Takes thoughtful and timely action when confronted with a problem. - Intermediate


• Ability to adapt to changes in assignments, flexibility, and willingness to work extended hours. - Intermediate


• Strong team player. - Intermediate

Specialized Knowledge:

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