 ##  [Site Engineering Manager, Manufacturing (Isotopes)](/req-10088994-site-engineering-manager-manufacturing-isotopes "Site Engineering Manager, Manufacturing (Isotopes)") 

  Job ID REQ-10088994 

 

 Oct 05, 2026 

 

 LOC_US 

 

 

 

###  About the Role 

## Key Responsibilities

  
- Provide strategic and day-to-day leadership for the Process Engineering and Maintenance departments supporting manufacturing process equipment, including applicable QC-adjacent equipment.
- Coach and develop engineers, maintenance professionals, reliability resources, and external service providers while remaining directly engaged in equipment troubleshooting, investigations, execution, and recovery when needed.
- Ensure equipment remains safe, compliant, qualified, reliable, and fit for intended use while owning site maintenance and asset-management programs, including preventive, predictive, and corrective maintenance activities.
- Drive equipment reliability strategies to improve performance and reduce unplanned downtime. Lead process and equipment engineering initiatives that improve process capability, equipment performance, throughput, yield, safety, product quality, and manufacturability
- Provide governance and oversight for commissioning, qualification, and validation activities, including lifecycle documentation, risk-based qualification, periodic review, requalification, and maintenance of the validated state.
- Lead engineering investigations, deviations, change controls, corrective and preventive actions, and technical risk assessments, ensuring timely closure and sustainable corrective actions.
- Maintain continuous inspection readiness for Engineering and Maintenance; serve as the site engineering subject matter expert during internal audits, health authority inspections, and regulatory commitments.
- Manage departmental operating and capital budgets, contractor performance, technical service agreements, and procurement activities to deliver compliant, cost-effective engineering support.

  
## Essential Requirements

- Bachelor's degree in Engineering, Computer Science, Automation, or a related technical field.
- Minimum 5 years of engineering, maintenance, reliability, process, or equipment experience within the chemical, pharmaceutical, biotechnology, or other regulated manufacturing industry.
- Experience hiring, leading, and developing technical resources in a cGMP environment, including a minimum of 3 years of people leadership experience managing and developing technical teams.
- In-depth knowledge of FDA regulations, Title 21 CFR Part 11, GAMP5, and GMP systems.
- Strong written and verbal communication skills with the ability to communicate equipment status, risks, priorities, and recommendations to diverse stakeholders.
- Ability to travel up to 10% as required.

  
The salary for this position is expected to range between $114,100 and $211,900 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

To learn more about the culture, rewards and benefits we offer our people click [here.](https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf)



 

###  Role Requirements 

 

**Why Novartis:** Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? [https://www.novartis.com/about/strategy/people-and-culture](https://www.novartis.com/about/strategy/people-and-culture "https://www.novartis.com/about/strategy/people-and-culture")

**Benefits and Rewards:** Learn about all the ways we’ll help you thrive personally and professionally.  
[Read our handbook (PDF 30 MB)](https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf)



 

 

 

 

 

 Division DIV_TO 

 

 Business Unit Production / Manufacturing 

 

 Location LOC_US 

 

 Site Indianapolis 

 

 Company / Legal Entity U469 (FCRS = US469) AAA USA Inc. 

 

 Functional Area FCT_TO 

 

 Job Type Full time 

 

 Employment Type Regular 

 

 Shift Work No 

 

 [Apply to Job](https://novartis.wd3.myworkdayjobs.com/en-US/Novartis_Careers/job/Indianapolis/Site-Engineering-Manager--Manufacturing--Isotopes-_REQ-10088994-1 "Apply to Job") <a class="link_button button_text" href=""></a> 

 

 

 

 

 

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 Job ID REQ-10088994 

 

 

###  Site Engineering Manager, Manufacturing (Isotopes) 

 [Apply to Job](https://novartis.wd3.myworkdayjobs.com/en-US/Novartis_Careers/job/Indianapolis/Site-Engineering-Manager--Manufacturing--Isotopes-_REQ-10088994-1 "Apply to Job") <a class="link_button button_text" href=""></a>