Evening Biotech Shift Leader – cGMP & Lean Excellence

Lonza Biologics, Inc. in; Vacaville (CA); On-site; USD 95,000 - 159,000; Full time

Benefits offered by this job

Performance-related bonus

Medical, dental and vision insurance

401(k) matching plan

Life insurance and disability

Employee assistance programs

Paid Time Off

Job summary

Lonza Vacaville is seeking a shift leader to manage site manufacturing operations in a fully onsite role. You will lead a team, ensure cGMP compliance, and drive Lean initiatives to improve efficiency, quality, and safety in a high-stakes biopharmaceutical setting.

The position requires AS/BS/BA in relevant fields and 5–6 years of supervisory biotech experience, with a proven track record of successful inspections and continuous improvement. Competitive salary and benefits are offered.

Qualifications

• AS/BS/BA in Biological Sciences, Physical Sciences, or Engineering preferred.
• Minimum 5-6 years supervisory experience in biotech/pharmaceutical industry.
• Proven track record of safe, compliant operations in a large-scale cGMP manufacturing environment.
• Experience leading cGMP-compliant operations through health authority inspections; aseptic/bioprocessing background preferred.
• Driven by Lean and continuous improvement methods to boost quality and productivity.
• Ability to lead and develop an operational staff in a dynamic setting.

Responsibilities

• Accountable for shift performance including budget management, productivity, labor efficiency, and achieving goals.
• Ensure cGMP compliance and inspection readiness at all times; support inspections.
• Produce high-quality products per Health Authority regulations and Lonza quality systems.
• Drive Lean and other continuous improvement initiatives for efficiency and quality.
• Lead, train, and develop manufacturing staff for qualification and accountability.
• Oversee equipment, facilities, and validated processes; coordinate maintenance and improvements.
• Manage deviations, investigations, validation strategies, and technical transfers with sustainable CAPAs.

Skills

Supervisory experience

Lean manufacturing

cGMP compliance

Quality systems

Bioprocessing

Education

AS/BS/BA in Biological Sciences, Physical Sciences, or Engineering

Job description

Lonza Vacaville is seeking a shift leader to manage site manufacturing operations in a fully onsite role. You will lead a team, ensure cGMP compliance, and drive Lean initiatives to improve efficiency, quality, and safety in a high-stakes biopharmaceutical setting.

The position requires AS/BS/BA in relevant fields and 5–6 years of supervisory biotech experience, with a proven track record of successful inspections and continuous improvement. Competitive salary and benefits are offered.