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

ESSENTIAL FUNCTIONS Facilitates Process Hazard Analysis (HAZOP) associated with Process Safety Management activities. Ensures a safe and quality working environment through training, awareness, and compliance to safety SOP's, corporate standards, EPA, and OSHA regulations. Contributes as a team member in analyzing and continually improving the site's Safety Culture. Exper

OF POSITION Perform basic quantitative and qualitative analyses of pharmaceutical components, in process material, finished good product, and/or stability product. Depending on the department to which the incumbent reports some of the functions listed may not be applicable. ESSENTIAL FUNCTIONS Perform basic analytical laboratory tests (such as potency, purity, uniformity,

The Sr Formulation Scientist will assume a key functional role within Global Technical Operations. The Sr Formulation Scientist will be responsible for providing formulation and aseptic fill/finish expertise for late stage drug product development and commercial manufacturing initiatives. This includes conducting laboratory scale formulation and fill/finish experiments fo

Salary range $46,000.00 $50,000.00 + $3,500.00 Sign On Bonus Samples Tested Perform basic analytical laboratory tests (such as potency, purity, uniformity, dissolution, moisture, etc.) in accordance with approved methodology and cGMP, FDA, and DEA regulations, including a. Set up, adjustment, calibration and operation of laboratory equipment and instruments, as well as an

The Manager, Controlled Substances Compliance position is part of the Controlled Substances Compliance Team within the Mallinckrodt Specialty Generics business. The Manager Controlled Substances Compliance role is vital to the Company's U.S. Drug Enforcement Administration (DEA) compliance function, which is a critical part of the continued success of the Company's Specia