A hands-on contributor, which performs repairs, planned maintenance and Non-Planned Maintenance (IE; improvements) to maintain the facility and facility related equipment at Noven Pharmaceuticals in a compliant and operational readiness state. This position is for support during the 3rd shift operations. This requires a person to be onsite to perform job as this is not a remote position.

Responsible for overall activities related to manufacturing and packaging of potential and existing products. Operate and maintain small production equipment.  Weigh, measure and check raw materials to assure batches manufactured contain proper ingredients and quantities.  Maintain records and cleanliness in compliance with cGMP, SOP, and Safety protocols.

Responsible for the support of manufacturing processes, instrumentation and equipment from manufacturing values stream and equipment maintenance. Integral part of the value stream team accountable for delivery of improvements in the areas of safety, quality, service and cost per the team goals and metrics. Provides expertise in engineering, design, process and/or scale-up. Assists manufacturing operation in problem solving with regards to materials, components, equipment and systems.  Develops and recommends new process solutions and technologies to achieve cost effectiveness and improved product quality.  Recommends process improvements to all products manufacturing areas, using tankage, piping, coating /oven systems, laminating dies, pouching machines,...

Perform Quality Assurance tasks such as sampling, inspections, and tests designed to ensure manufactured products are in compliance with internal SOP’s, Safety initiatives, Company policies, FDA and DEA regulations.  Document all work performed, ensuring accuracy and thoroughness.  Inform management of any deviations from established standards/procedures.

Perform Quality Assurance tasks such as sampling, inspections, and tests designed to ensure manufactured products are in compliance with internal SOP’s, Safety initiatives, Company policies, FDA and DEA regulations.  Document all work performed, ensuring accuracy and thoroughness.  Inform management of any deviations from established standards/procedures.

Provide technical support to manufacturing, engineering and other departments / teams by ensuring maximum equipment uptime, and addressing technical challenges. When not supporting manufacturing, technician shall perform scheduled PMs in timely manner as required by the CMMS system for work orders. Lastly, under limited supervision, performs and documents moderately complex technical functions relating to test, layout, quality control, fabrication, modification and assembly of mechanical equipment and/or components. 

The Sr Director Trade & Market Access is responsible for overseeing and leading the management of Noven trade partnerships and optimizing patient services to ensure the effective distribution and accessibility of our products.  This role will be responsible for developing, enhancing and implementing strategic business opportunities with key partners.

The Mfg Operator BC performs all the general duties and operations to manufacture the product. An operator will operate machines and handle components using prescribed standard operating procedures and cGMP guidelines to manufacture and ensure the product meets the quality requirements. The operator will complete the necessary documentation and records to maintain quality control.