Process Engineer III
Job in
Durham, Durham County, North Carolina, 27701, USA
Listed on 2026-06-08
Listing for:
Novartis AG
Full Time
position Listed on 2026-06-08
Job specializations:
-
Engineering
Quality Engineering, Validation Engineer, Manufacturing Engineer, Process Engineer
Job Description & How to Apply Below
Step into a pivotal engineering role where your expertise directly shapes advanced manufacturing operations. As a Process Engineer III, you will support the design, validation, maintenance, and lifecycle management of manufacturing equipment, facilities, and utilities. This role requires hands-on experience with automated and manual visual inspection systems and drug product/fill-finish equipment to ensure compliant, reliable, and efficient GMP operations.
About the Role
Location:
* This position will be located in Durham, NC and will be an onsite role.
* Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.
Key Responsibilities:
* Bachelor's degree in Chemical, Electrical, or Mechanical Engineering or related technical field
* Minimum 5 years pharmaceutical or biopharmaceutical GMP manufacturing experience, or equivalent experience
* Strong knowledge of FDA regulations and GMP systems
* Demonstrated experience supporting engineering activities in a regulated pharmaceutical or biotechnology environment
* Experience with automated and manual visual inspection equipment, as well as general drug product / fill-finish production equipment
* Proven ability to lead cross-functional teams in a fast-paced and dynamic setting
* Strong project management skills with experience in both strategic and long-term planning
* Excellent written and verbal communication skills with strong technical writing capabilities
* Ability to analyze complex issues and implement effective, compliant engineering solutions
Essential Requirements:
* Bachelor's degree in Chemical, Electrical, or Mechanical Engineering or related technical field
* Minimum 5 years pharmaceutical or biopharmaceutical GMP manufacturing experience, or equivalent experience
* Strong knowledge of FDA regulations and GMP systems
* Demonstrated experience supporting engineering activities in a regulated pharmaceutical or biotechnology environment
* Proven ability to lead cross-functional teams in a fast-paced and dynamic setting
* Strong project management skills with experience in both strategic and long-term planning
* Excellent written and verbal communication skills with strong technical writing capabilities
* Ability to analyze complex issues and implement effective, compliant engineering solutions
Novartis Compensation and Benefit
Summary:
The salary for this position is expected to range between $98,700 and $183,300 annually
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.
#LI-Onsite
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?
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