ProcessEngineerIII

**Job Description Summary** 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. **Job Description** **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 pharmaceutic