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Engineer, Process Engineering - Bloomington Indiana
Company: Disability Solutions Location: Bloomington, Indiana
Posted On: 05/18/2024
Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives.--Process Engineering focuses on developing processes to minimize risks to the product. The Engineering department is responsible for supporting CGMP operations through process engineering, facilities and utilities engineering, calibration, process improvement and automation, packaging, capital projects, while maintaining compliance with regulatory standards.--The Engineer, Process Engineering, will support ongoing activities by assisting in troubleshooting mechanical problems, identifying improvements in utilities to minimize interruptions (down time) and reduce energy usage/cost, and supporting new and ongoing projects. This position will further assist in the management and planning of project budgets and schedules and provide contractor oversight. This position will assist in identifying, tracking, forecasting, and implementing capital expenditure projects by working with site leadership and departmental end users to identify the correct project parameters and utility requirements. The Engineer may establish new Standard Operating Procedures (SOPs) and/or recommend changes to current SOPs based on facility needs. This person will work on complex facility-related problems requiring in-depth data analysis to determine appropriate action. The Engineer is expected to have extensive ongoing communication with employees and cross-functional group managers/departments on facility-related issues.This is a fulltime role working days; Monday - Friday This position offers a $5,000 sign on bonusCatalent Pharma Solutions in Bloomington, Indiana is a state-of-the-art, GMP manufacturing facility, providing one million sq/ft of drug substance manufacturing, drug product manufacturing, and related pharmaceutical services. This award-winning facility helps customers accelerate biologic drug development programs and bring better treatments to help patients live better healthier lives.--Catalent is committed to a Patient First culture through excellence in quality and compliance and to the safety of every patient, consumer, and Catalent employee.The Role: - Support selection and installation of manufacturing equipment
- Proactively and effectively partner with the facility commissioning/validation team, including operational protocol development, to implement compliance with FDA GMP requirements
- Draft SOPs for building operation, maintenance, and calibration
- Develop critical recipes for the Automated Inspection Machine (AIM)
- Identify improvements and efficiencies
- Provide engineering guidance and execution on projects
- Perform hands-on activities as needed to help troubleshoot AIM related problems
- Communicate with clients and vendors to ensure the integrity of validated inspection recipes and ensure accurate tech transfer
- Other duties as assignedThe Candidate:
- Bachelor's degree in Chemical/Mechanical/Electrical Engineering or appropriate scientific discipline, required, or 8 years of engineering experience in lieu of the degree
- PE / Registered Engineer in training, preferred
- OSHA 10 or equivalent, preferred
- 2+ years of Project Engineering related experience
- Statistics experience/knowledge, preferred
- Must be able to read and understand English-written job instructions and safety requirementsWhy You Should Join Catalent
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