The Thought Leader Liaison (TLL) is responsible for developing, managing, and engaging with Key Opinion Leaders throughout their assigned geography reporting to the Thought Leader Liaison Lead, reporting through Specialty Brands Marketing. He/she works closely with commercial colleagues and other staff to help build advocacy of Mallinckrodt's products with KOLs. TheThough

The Thought Leader Liaison (TLL) is responsible for developing, managing, and engaging with Key Opinion Leaders throughout their assigned geography reporting to the Thought Leader Liaison Lead, reporting through Specialty Brands Marketing. He/she works closely with commercial colleagues and other staff to help build advocacy of Mallinckrodt's products with KOLs. TheThough

The Senior Director, Clinical Development Medical Affairs (CDMA) drives strategy and accountability for the nitric oxide drug and device program execution, ensuring alignment with brand team objectives, incorporation of relevant internal and external insights and the generation of an R&D plan that delivers for unmet patient need, generates competitive differentiation, and

Strategic Planning and Coordination Develop and coordinate pre launch and launch activities, including leading launch kickoff meetings, conducting Launch Readiness Reviews, and acting as a thought partner with the brand lead. Create and lead the implementation of a strategic roadmap and operational direction for the launch process, ensuring alignment across functions. Cro

Blend defined quantities of designated raw materials (per specific manufacturing instructions) into final dosage blend stage. Executes all production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Blending Technician is exp

The Quality Control (QC) Manager is responsible for leading the QC function at the Port Allen, LA manufacturing facility. The QC Manager oversees quality inspections, material characterization, and qualification in production operations. They also ensure compliance in deviation investigations, validation studies, and site level research. Essential Functions Lead developme

The Operations Shift Supervisor is responsible for the Safety, Quality, and cost Effectiveness of the maintenance and manufacturing operations in his/her area. The Operations Shift Supervisor will also serve as Incident Commander or Incident Operations during a plant incident. The Operations Shift Supervisor operates as the site leader on off shifts and weekends. Operatio

Responsible for continually monitoring processes and procedures primarily for inventory control of controlled substances active pharmaceutical ingredient (API) and finished dose, preparation of U.S. Drug Enforcement Administration (DEA) controlled substances quota requests and reporting of controlled substances transactions in accordance with state and federal controlled

Works with respective functional group in developing and implementing project scope and cost estimates. Works with respective functional group(s), incorporating business data (sales, financial, etc.) where appropriate, to generate a compelling project justification and application for approval of funds. Works with all internal stakeholders to develop User Requirement Spec

The successful candidate will be able to show documented success as a top producer using superior clinical selling skills, while effectively managing their territory operating within all compliance and company policies and procedures, as a results oriented sales person, business partner and consultant. Develop strategically targeted, accounts and specific business plans t

The Senior Director, Clinical Development Medical Affairs (CDMA) drives strategy and accountability for the hepatology drug program execution, ensuring alignment with brand team objectives, incorporation of relevant internal and external insights and the generation of an R&D plan that delivers for unmet patient need, generates competitive differentiation, and prepares for

ESSENTIAL FUNCTIONS Diagnose plant equipment problems. Perform preventive maintenance procedures. Routine repairs to electrical equipment in accordance with all plant work instructions and safety procedures. Perform safety observations as needed. Maintain equipment in area of responsibility. Perform inspections of electrical equipment. Troubleshoot electrical failures usi

OF POSITION The Manager Plant Quality II directs the operation of the Greenville Quality Department to ensure product quality and regulatory compliance. The Quality Manager will champion the continued transformation of the Greenville Site to pharmaceutical finished drug product standards while achieving stated departmental and business objectives. The Quality Manager will

OF POSITION Depending on the laboratory area, will perform analysis on Raw Materials, Intermediates, In Process, Finished Product, or Stability samples using established analytical methods. ESSENTIAL FUNCTIONS Follow good documentation practices for the accurate and timely documentation of all activities. Perform wet chemistry and instrumentation testing. Follow site HSE P

OF POSITION The primary responsibility of this position is working with Production Operators in the transfer and shipping of controlled substances from the St. Louis Plant as well as serving as a back to the vital functions of the custom packaging operations of the controlled substances business. This position is responsible for coordinating controlled substance moves thro