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Principal Engineer, Facilities

1 month ago


Bloomington, United States Catalent Inc Full time

Principal Engineer, Facilities & Maintenance 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 Principal Engineer, Facilities & Maintenance, serves as a subject matter expert supporting 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. There is a $10,000 sign on for this role. 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: Investigate and document technical problems for identified non-conformances. 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. Identify improvements and efficiencies of facility preventative maintenance; help drive department continuous improvement projects related to department metrics. Perform hands-on activities, often partnering with the maintenance, as needed to serve as an escalation point for help in troubleshooting facility problems and support facility staff. Respond to customer/regulatory audit observations and corrective actions as it pertains to automation system validation. Assist Manager in candidate selection process. Other duties as assigned. The Candidate: Bachelor's degree in Chemical/Mechanical/Electrical Engineering or appropriate scientific discipline, with 8+ years of relevant experience, required. Master’s degree, preferred. PE / Registered Engineer in training a plus. OSHA/IOSH/NeBOSH Certification or equivalent, preferred. 3+ years within the pharmaceutical or biotechnology industry with a focus on sterile biologics manufacturing, inspection and/or packaging. Must be able to read and understand English-written job instructions and safety requirements. Why You Should Join Catalent: Competitive medical benefits and 401K. 152 hours of PTO + 8 Paid Holidays. Dynamic, fast-paced work environment. Opportunity to work on Continuous Improvement Processes. Catalent offers rewarding opportunities to further your career Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone’s safety. The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. #J-18808-Ljbffr