Accountable for the growth and profitability of Aenova’s Contract Development Manufacturing Organization (CDMO) business. - Manage and grow existing customer base via strategic relationship management - Identify and manage new business opportunities - Develop and manage budgets and forecasts - Increase access to and visibility of the Aenova organization within North America

Pfizer CentreOne is a leading provider of contract manufacturing services offering biopharmaceutical companies unparalleled knowledge, experience, and expertise in injectable drug product and API manufacturing. Specific focuses include:• Sterile injectable fill-finish (small molecule and biologic)• Small-molecule steroid and hormone intermediates and APIs• Custom small-molecule API synthesis

Expat assignment supporting Hospira’s green field site located in Visakhapatnam, India. Responsibilities include the oversight of activities related to the qualification and start-up of all aseptic filling operations.

Manufacturing business unit manager with oversight of the Dispensing, Compounding, Component Prep, and Equipment Prep departments, leading 10 direct reports and approximately 150 non-exempt employees. Directly responsible for approximately $45MM in Hospira raw materials and $150 to $200MM in third party API drug product. Maintaining cGMP compliance in the department while meeting the production schedule and reducing downtime. Resolve complex issues; compile, analyze and report on key performance metrics to support decision-making; allocate and adapt resources to maximize effectiveness.

Responsible for the contract manufacturing development team and multiple third party accounts, acting as a liaison between the One2One business and the Hospira McPherson site. Coordinated all activities associated with the manufacturing, release, and shipping of commercial product. Ensured compliance with all regulatory and legal requirements. Extensive interaction across site functions and departments as well as with suppliers and customers.

Senior supervisor role over a 24/7 compounding and dispensing operation, leading a department of approximately 30 team members. Tracked and monitored the manufacturing schedule, coordinating all activities related to dispensing, API thaw, product hold times, and all related activities associated with the formulation of several hundred Hospira and third party product formulations. Ensured a thorough review of batch records for accuracy and completeness; authoring deviations, and identifying corrective and preventative actions as necessary. Maintained cGMP compliance within the department.

Supervised both terminal and aseptic filling lines, along with multiple packaging lines. Intimately involved in day to day operations, including scheduling and execution of batches. Responsibilities included the planning and effective use of labor and materials while maintaining quality. Responsible for approximately 65 non-exempt employees.

R&D chemist responsible for 3rd party method development, technical transfers, assay validations, and cleaning validations supporting Manufacturing, Validations, and the One2One Contract Manufacturing business. Proficient in analytical techniques requiring HPLC, GC, UV, FTIR, KF Titration.