Senior Process Engineer at Fusion Life Sciences Technologies LLC Senior Process Engineer at Fusion Life Sciences Technologies LLC in Greenville, North Carolina Posted in about 12 hours ago.

Type:

full-time Senior Process Engineer -

Pharmaceutical Manufacturing Location:

Greenville, NC Work Arrangement:

Onsite Contract Duration:

12+

Months Job Type:

Contract Position Overview Our client, a growing pharmaceutical CDMO, is seeking a Senior Process Engineer to drive process improvements across the manufacturing site. The ideal candidate will have hands-on experience with aseptic processing, automated vial filling equipment, isolators, and cGMP manufacturing environments . Key Responsibilities Optimize fill line and isolator performance to improve reliability, efficiency, and throughput. Troubleshoot aseptic processing and manufacturing issues in a cGMP environment . Support and improve EMA and Optima filling lines , including automated vial filling equipment. Investigate process deviations and equipment/process performance issues and implement effective corrective actions. Support formulation, filling, and autoclave operations . Partner with Manufacturing, Engineering, Quality, Maintenance, and other cross-functional teams. Identify opportunities for continuous improvement, process optimization, and reliability enhancement. Develop, revise, and maintain SOPs, batch records, work instructions, and other process documentation . Provide hands-on technical support in a fast-paced pharmaceutical manufacturing environment. Apply engineering principles and data-driven problem-solving to improve process performance and equipment reliability. Required Skills & Experience Strong experience in Process Engineering within pharmaceutical/biopharmaceutical manufacturing. Hands-on experience with aseptic processing and troubleshooting . Experience with automated vial filling/fill-finish operations . Experience with Optima H610 filling equipment strongly preferred. Experience with EMA fill lines preferred. Understanding of isolator systems and associated support equipment. Familiarity with autoclave processes and formulation/filling operations. Strong understanding of cGMP requirements . Experience creating and maintaining SOPs, batch records, and process documentation . Strong troubleshooting, root-cause analysis, and continuous improvement skills. Reliability Engineering experience is a plus. Ability to work onsite in Greenville, NC .