Supervisor I or II, Manufacturing Operations

Are you ready to join a growing, global drug development and manufacturing organization that puts people first?  Come to Adare!  We work closely with our pharmaceutical industry partners during all phases of drug development and commercial manufacturing with a mission of improving the lives of patients and medicines essential to people all over the world.  Every role within Adare offers you a unique, customized experience with a chance to make a real impact that is critical to our success.  With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!

Join our mission at Adare!

What can Adare offer you?


* Medical/dental/vision/life – low employee premiums


* 401k with a highly competitive match


* Generous PTO, including floating holidays


* Career growth and internal opportunities


* Tuition reimbursement


* Relocation assistance


* Performance-based bonus


* Employee Recognition Programs

 

We are seeking to hire a Supervisor I or II to join our Manufacturing Operations team…

If any of the below describes you, we would love to meet you! 

Job Summary

The Supervisor I or II is to assume responsibility for all production activities, control of production processes and development of employees on their respective shift.  It is also to assure production schedules and requirements are satisfied, in addition to other daily functions needed or requested by Manufacturing Management.

 

Responsibilities and Learning Opportunities


* Supervision of daily and monthly tasks within the manufacturing/operations department and be help responsible and accountable for all activities in production areas.


* Support and promote Safety and cGMP programs, ensuring strict conformance to all current FDA and cGMP guidance’s and guidelines.


* Execute all operational plans to optimize capacity/utilization of equipment and personnel to deliver product on time to our internal as well as external customers.


* Perform the computerized inventory transactions needed to assure compliance with master formulae, and to provide the data Logistics and Finance required to track inventory/supply needs, and evaluate business volumes.  Ensures conformance with all current FDA and cGMP guidance’s and guidelines.


* Report any deviations from the schedule promptly to Management and Logistics, and takes all steps possible to minimize downtime of scheduled production.


* Assist Technical Services Group with the execution of experimental and validation projects that use process equipment and facility.


* Assure processes are performed according to Standard Operating Procedures (SOPs) to ensure the quality of the product.


* Routinely monitor facility and equipment status and promptly take steps (through work orders, operator action, etc.) to get repairs made, prevent damage, or protect personnel.  Follow up on these actions.


* Insist on ...