Manufacturing Operations Lead for Gene Therapy Startup

BioSpace; Lebanon (IN); On-site; USD 66,000 - 145,000; Full time

Benefits offered by this job

Company bonus

401(k) plan

Pension

Vacation benefits

Health insurance

Well-being benefits

Job summary

Lilly is a global leader in biopharmaceuticals, currently starting up a state-of-the-art manufacturing facility in Lebanon, Indiana dedicated to gene therapy. This Manufacturing Operations Associate role focuses on startup delivery, process design, and ramping GMP production efficiencies in a fast-paced environment.

You will partner with Engineering, Tech Services, and Quality & Regulatory, building deep operating expertise and driving data-driven decisions to ensure continuous improvement and

Qualifications

• Bachelor's degree in engineering or related technical field.
• 5+ years of Operational, Engineering, Technical Services, or Pharmaceutical Manufacturing Experience.
• Authorized to work in the United States on a full-time basis; Lilly will not sponsor visas.

Responsibilities

• Assist Process Team Leaders by leading Process Teams with focus on safety, quality and manufacturing performance.
• Ensure cGMP readiness of manufacturing areas for startup and process qualification activities; support training and runs.
• Support validation activities and maintain GMP production areas in compliance and in a validated state.
• Promote a safety-first culture with accountability and safe systems of work.
• Lead or participate in continuous improvement projects; contribute to the Operational Excellence Roadmap for LP2 Flow Team.
• Collaborate with Engineering, Tech Services, Quality & Regulatory to troubleshoot processes and drive improvements.

Education

Bachelor's degree in engineering or related technical field

Job description

Lilly is a global leader in biopharmaceuticals, currently starting up a state-of-the-art manufacturing facility in Lebanon, Indiana dedicated to gene therapy. This Manufacturing Operations Associate role focuses on startup delivery, process design, and ramping GMP production efficiencies in a fast-paced environment.

You will partner with Engineering, Tech Services, and Quality & Regulatory, building deep operating expertise and driving data-driven decisions to ensure continuous improvement and