Director, Non-Sterile Manufacturing & Packaging

ThermoFisher Scientific; Greenville (NC); In loco; USD 180.000 - 230.000; Tempo pieno

Descrizione del lavoro

Thermo Fisher Scientific in Greenville, NC seeks a Director of Non-Sterile Operations to lead and optimize non-sterile manufacturing, packaging, inspection, and device assembly. You will oversee OSD and Continuous Manufacturing platforms, driving safety, quality, and cost performance from development to commercialization.

Responsibilities include ensuring cGMP compliance, guiding technology transfer, and building high‑performing cross-functional teams across packaging, device assembly, and CM

Competenze

• Bachelor’s degree in Engineering, Operations Management, or related field (or equivalent experience).
• 10+ years of progressive operations leadership in pharmaceutical/biopharmaceutical manufacturing, including sterile manufacturing in a regulated environment.

Mansioni

• Lead and oversee non-sterile operations focusing on packaging, inspection, and Auto Injector Assembly.
• Own operational performance across safety, quality, delivery, cost, and people with accountability and measurable results.
• Strengthen capabilities through operational rigor, process robustness, and technology enablement.
• Ensure sustained cGMP compliance through quality systems, documentation, investigations, CAPA, and risk management.
• Support technology transfer, scale-up, and commercialization across packaging, device assembly, OSD, and CM programs.
• Develop high-performing teams and foster a culture of engagement and continuous improvement.

Conoscenze

Operations leadership

Regulatory compliance

Continuous improvement

Strategic financial acumen

Travel readiness

Formazione

Bachelor’s degree in Engineering or related field

Strumenti

Automated assembly systems

Continuous manufacturing technologies

CAPA systems

Descrizione del lavoro

Thermo Fisher Scientific in Greenville, NC seeks a Director of Non-Sterile Operations to lead and optimize non-sterile manufacturing, packaging, inspection, and device assembly. You will oversee OSD and Continuous Manufacturing platforms, driving safety, quality, and cost performance from development to commercialization.

Responsibilities include ensuring cGMP compliance, guiding technology transfer, and building high‑performing cross-functional teams across packaging, device assembly, and CM