Process Engineer

Job Summary:

Responsible for leading product technology transfer and process scale-up for new and existing thin film and dispensed LCO (Lotion, Cream, Ointment) pharmaceutical products at Aquestive Therapeutics Manufacturing facilities in Portage, IN. 

Responsibilities:

• Lead New and Continuous Process Improvement Projects, including identification of opportunities, researching literature and vendors for new technologies, preparing/presenting proposals, developing/executing projects, while following appropriate Management of Change (MOCs) methodologies.
• Support day-to-day manufacturing operations as Technical Subject Matter Expert (SME) by investigating and resolving process related issues involving the manufacturing process or equipment/ systems
• Perform process monitoring of identified attributes and process parameters. Identifying trends and appropriate actions to continuously improve the process and product.
• Provides training support as required.
• Supports development of required cleaning processes for equipment trains.
• Prepares documentation for new processes and process improvements including Management of Change (MOCs), Risk Assessments, Batch Records, Engineering Studies (ES) and Standard Operating Procedures (SOPs)
• Prepare Work Orders (WOs), Management of Change (MOCs), Design Specifications (DS), User Requirements Specifications (URS), System Specifications Documents (SSD), Failure Mode and Effect Analysis documents (FMEA) for new system/ processes.
• Develops a plan and leads product technology transfer and scale-up.
  • Determines process parameters at Pilot and Commercial Scale.
  • Evaluates process parameter variability on Critical Quality Attributes.
  • Establishes the product manufacturing control strategy and implements into Batch Records.
  • Finalizes the QTPP (Quality Target Product Profile).
• Represents Engineering Subject Matter Expert (SME) in Product Development Teams.
• Support deviation investigations to identify root causes and define corrective and preventive actions (CAPAs).
• Work with and manage outside contractors to provide support to projects.
• Able to perform all duties efficiently and independently with minimal supervision.
• Able to work within and lead in a team environment, consisting of multi-functional groups, to achieve a common goal, while promoting teamwork, timeliness, accuracy and compliance in all activities.
• Able to interact with management and peers within the department, within the plant, within the organization and outside regulatory agencies. The individual must also interact with vendors, sub-contractors and consultants on a routine basis. 

• This position requires concentrated effort in recording, evaluating and transcribing data, as well as computer work, which can cause mental and/or eye fatigue. The work is performed in a clean environment.
• This position will provide 24-hour support for manufacturing and may be required to work extended hours to support operations or projects.