Senior Automation Engineer

• Serve as system owner and automation subject-matter expert ensuring reliable operation of manufacturing and facility automation systems.
• Troubleshoot production-impacting issues involving PLCs, SCADA/HMI systems, historians, alarms, industrial networks, and OEM equipment.
• Support manufacturing, Facilities, and Utilities teams when automation issues arise and perform root cause investigations with long-term corrective actions.
• Provide after-hours escalation support for critical system failures.
• Act as technical owner for assigned automation systems, monitoring performance, reliability, and data integrity.
• Identify opportunities to improve uptime, maintainability, cybersecurity, and system effectiveness.
• Coordinate with vendors and integrators for support and upgrades.
• Lead automation workstreams for equipment installations and capital projects, including user requirements, design reviews, FAT/SAT, commissioning, qualification, startup, and handoff.
• Author and review change controls, deviations, CAPAs, risk assessments, SOPs, technical specifications, and lifecycle documentation.
• Ensure systems remain compliant with cGMP, GAMP, and Data Integrity requirements.
• Support audits and regulatory inspections as the system subject-matter expert.
• Mentor Automation Engineers I and II, review technical work, and lead cross-functional technical discussions.
• Coordinate activities with Quality, Validation, MS&T, Operations, Facilities, and Engineering teams.

• Bachelor's degree in Engineering, Information Technology, Computer Science, Automation, Electrical Engineering, Chemical Engineering, or related technical field with 5-8 years of relevant experience, or Associate degree in a related technical field with 7-10 years of relevant experience.
• 5+ years supporting automation systems in GMP manufacturing environments.
• Experience with PLC, SCADA/HMI, Historian, industrial control systems, and instrumentation.
• Experience leading automation projects, system upgrades, and troubleshooting efforts.
• Experience managing change controls, deviations, investigations, and CAPAs.
• Experience supporting validated systems within regulated manufacturing environments.
• Ability to stand, walk, bend, and climb stairs or ladders regularly throughout the workday.
• Ability to lift and carry up to 30 pounds occasionally.
• Manual dexterity to operate laptops, tools, instrumentation, and testing equipment.
• Ability to visually inspect equipment, read control panels, instrumentation, and technical documentation (corrected vision acceptable).
• Ability to work in tight or awkward spaces, including behind equipment and within cleanroom utility areas when troubleshooting or supporting projects.
• Ability to sit for extended periods while preparing technical documentation, reports, investigations, and engineering deliverables.
• Must be able to wear required PPE, including safety glasses/goggles, gloves, lab coats, and respiratory protection when required.

• Biopharmaceutical manufacturing
• Cell & Gene Therapy
• Vaccine manufacturing
• CDMO organizations
• Sterile injectable manufacturing

• Defined career path and annual performance review and feedback process
• Diverse, inclusive culture
• Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
• Competitive paid time off + 8 paid holidays
• Community engagement and green initiatives
• Medical, dental and vision benefits effective day one of employment
• Tuition Reimbursement

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: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond - it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE .