What are the responsibilities and job description for the Supervisor, Transdermal position at Amneal?
Job Summary
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.
Qualifications:
Education
- Bachelors Degree (BA/BS) in Related field - Preferred
- Associate Degree in Related field 5 yrs experience leading and training staff - Required
Work Experience
- 3 years or more in Transdermal drug delivery or manufacturing GMP environment - Required
- 3 years or more in Leading and training staff - Required
Skills and Abilities
- 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