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 Senior 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
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 utility equipment
- Partner with the facility commissioning/validation team, including operational protocol development, to implement and requalify equipment in compliance with requirements
- Draft SOPs for building operation, maintenance, and calibration
- Identify improvements and efficiencies of facility preventative maintenance
- Perform hands-on activities, often partnering with the maintenance, as needed to help troubleshoot facility problems and support facility staff
- Assist in responding to customer/regulatory audit observations and corrective actions
- Collaborate significantly with cross functional groups including Validation, Quality Engineering, Manufacturing, Process Development, and Facilities
- Other duties as assigned
The Candidate:
- Bachelor's degree in Chemical/Mechanical/Electrical Engineering or appropriate scientific discipline, with 5-8 years of relevant experience, required
- Master’s degree, preferred
- PE / Registered Engineer in training, preferred
- OSHA 10 or equivalent, preferred
- 5+ years of Project Engineering relevant experience, preferred
- 2+ years within the pharmaceutical or biotechnology industry with a focus on sterile biologics manufacturing, inspection and/or packaging preferred
- Highly skilled and/or certified in multiple trades
- 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.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
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. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
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