Process Engineer III

As a Process Engineer III, you will support the design, validation, maintenance, and lifecycle management of manufacturing equipment, facilities, and utilities to ensure compliant, reliable, and efficient GMP operations, including automated and manual visual inspection systems and drug product/fill-finish equipment.

Location: Durham, NC (onsite). Novartis is unable to offer relocation support.

Key Responsibilities / Qualifications:
- Bachelor’s degree in Chemical, Electrical, or Mechanical Engineering (or related technical field).
- 5+ years pharmaceutical/biopharmaceutical GMP manufacturing experience (or equivalent).
- Strong knowledge of FDA regulations and GMP systems.
- Experience supporting engineering activities in a regulated pharmaceutical/biotechnology environment.
- Experience with automated/manual visual inspection equipment and drug product/fill-finish production equipment.
- Ability to lead cross-functional teams in a fast-paced environment.
- Strong project management skills (strategic and long-term planning).
- Excellent written/verbal communication with strong technical writing.
- Ability to analyze complex issues and implement compliant engineering solutions.

Compensation & Benefits (as stated):
- Salary range: $98,700–$183,300 annually.
- Performance-based cash incentive; eligibility for annual equity awards (depending on level).
- Comprehensive benefits (health, life, disability, 401(k) with match) and time off (vacation, personal days, holidays, other leaves).