Process Engineer III
Listed on 2026-06-18
-
Engineering
Validation Engineer, Quality Engineering, Manufacturing Engineer, Process Engineer -
Manufacturing / Production
Validation Engineer, Quality Engineering, Manufacturing Engineer
Band Level 3 Process Engineer III
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.
Location:
Durham, NC (onsite). No relocation support.
• Design and validate manufacturing equipment and facilities.
• Maintain and manage lifecycle of equipment, utilities, and production lines.
• Support visual inspection systems and drug product/fill‑finish equipment.
• Ensure compliance with GMP, FDA regulations, and internal quality systems.
• Lead cross‑functional teams and drive continuous improvement.
Qualifications- Bachelor’s degree in Chemical, Electrical, or Mechanical Engineering or related technical field.
- Minimum 5 years of pharmaceutical or biopharmaceutical GMP manufacturing experience, or equivalent.
- Strong knowledge of FDA regulations and GMP systems.
- Experience supporting engineering activities in a regulated pharmaceutical or biotechnology environment.
- Proven ability to lead cross‑functionally in a fast‑paced, dynamic setting.
- Strong project management skills with experience in both strategic and long‑term planning.
- Excellent written and verbal communication skills and strong technical writing capabilities.
- Ability to analyze complex issues and implement effective, compliant engineering solutions.
- Business Continuity
- Change Control
- Cost Management
- Data Analytics and Digital
- Engineering Technical Expertise
- GDP Knowledge
- GMP Knowledge
- HSE Knowledge
- Knowledge of Relevant Tools and Systems
- Manufacturing Process (Production)
- Operational Excellence
- Quality Compliance
- Resilience and Risk Management
- Total Productive Maintenance
Salary range: $98,700 to $183,300 annually. Salary determined by skills and experience; reviewed periodically. Includes performance‑based cash incentive and potential eligibility for equity awards. Eligible US employees receive a comprehensive benefits package including health, life and disability insurance, 401(k) plan with company match, generous paid time off, and other benefits.
EEO StatementThe Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.
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