Manager, Process Engineering
@ 37-1755209 Patheon Manufacturing Services LLCManager, Process Engineering
About the job
Join Thermo Fisher Scientific's Pharma Services Group in Greenville, NC, to lead sterile manufacturing process engineering supporting drug development and production.
Requirements
- 6+ years in pharmaceutical manufacturing
- Experience with sterile fill/finish
- 3+ years in team leadership
- Troubleshooting manufacturing issues
- Supporting tech transfers and changeovers
Qualifications
- Bachelor's in Engineering or related field
- Strong collaboration skills
- Hands-on troubleshooting experience
Full job description
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale.
About the Business
Join our Pharma Services Group (PSG)—a global leader providing integrated drug development and manufacturing solutions to pharmaceutical and biotech companies. Our Greenville, North Carolina site specializes in sterile and oral solid dose (OSD) manufacturing.
Discover Impactful Work
The Manager, Process Engineering will lead a team supporting sterile manufacturing operations within Sterile South (vial, syringe, and auto-injector lines).
A Day in the Life
- Lead ~5 process engineers
- Provide hands-on support on the manufacturing floor
- Troubleshoot issues and perform root cause analysis
- Support tech transfers and changeovers
- Drive process improvements and efficiency
- Collaborate with quality, operations, maintenance, and engineering teams
- Mentor and develop team members
Keys to Success
Education
- Bachelor’s degree in Engineering, Science, Chemistry, Biology, or related technical discipline
Experience
- 6+ years of experience in pharmaceutical manufacturing with direct experience in sterile fill/finish operations (required)
- Minimum 3+ years of leadership experience, leading engineers or technical teams in a manufacturing environment
- Strong hands-on experience with:
- Troubleshooting manufacturing/process issues on the floor
- Root cause analysis and corrective actions
- Experience supporting tech transfer, changeovers, and new product introductions
- Experience partnering with operations to drive process improvements, efficiency gains, and performance optimization
- Exposure to equipment capabilities, line performance, and manufacturing constraints within sterile environments
Knowledge, Skills, Abilities
- Strong sterile manufacturing expertise
- Hands-on troubleshooting capability
- Strong collaboration and communication skills
Competencies
Technical Problem Solving, Leadership, Continuous Improvement, Collaboration, Execution
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