Automation Engineer
Actalent
Automation Engineer
The Automation Engineer is responsible for ensuring the reliable, compliant, and continuous operation of sterile pharmaceutical manufacturing systems within a regulated cleanroom environment. This role is heavily hands-on and supports day-to-day manufacturing by installing, maintaining, calibrating, and troubleshooting automation hardware, process instrumentation, electrical systems, and clean utility infrastructure used in aseptic production. The position combines field-level electrical and instrumentation work with controls system support, including PLC, HMI, SCADA, BMS, and EMS platforms. The engineer performs equipment installation, wiring, panel modifications, loop checks, functional testing, and commissioning activities while supporting validation efforts such as FAT/SAT and IQ/OQ/PQ. A strong emphasis is placed on cGMP compliance, FDA 21 CFR Part 11, data integrity, and audit-ready documentation. This role also supports critical pharmaceutical utilities such as PW, WFI, Clean Steam, CIP/SIP, HVAC, and HEPA-controlled environments, ensuring systems meet cleanroom classification and environmental monitoring requirements. The engineer works extensively with sensors, transmitters, motors, drives, actuators, and automated machinery, diagnosing issues and implementing corrective and preventive maintenance strategies. In addition to technical execution, the Automation Engineer maintains detailed calibration records, CMMS entries, and validation documentation, and participates in root-cause analysis and CAPA implementation. The position requires comfort working in ISO 5/7/8 cleanrooms, wearing full gowning, navigating elevated platforms, and performing physical, hands-on work across rotating or extended shifts in a regulated manufacturing setting.
Plc programming, SCADA, Electrical, Troubleshooting
Plc programming, SCADA, Electrical, Troubleshooting
BE – Mechanical/Chemical from a reputed University Minimum 3 to 10 years of professional experience in the field of pharmaceutical or manufacturing industry. Experience supporting GMP audits and inspections Familiarity with change control and deviation processes Basic knowledge of industrial communication networks Exposure to manufacturing data or automation systems Ability to work closely with Quality, Validation, and Production teams Strong prioritization skills in fast-paced manufacturing environments
This is a Permanent position based out of Sacramento, CA.
The pay range for this position is $75000.00 - $95000.00/yr. Yearly bonus eligibility Benefits: Nivagen offers a wide variety of benefits and programs to support health and well-being, including medical, dental, and vision coverage Paid time off plan 401k savings plan
This is a fully onsite position in Sacramento, CA.
This position is anticipated to close on Apr 1, 2026.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:
- Hiring diverse talent
- Maintaining an inclusive environment through persistent self-reflection
- Building a culture of care, engagement, and recognition with clear outcomes
- Ensuring growth opportunities for our people
Actalent is an equal opportunity employer.
About Actalent
Actalent is a global leader in engineering and sciences services. For more than 40 years, we've helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.
Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands.