Manufacturing Supervisor

Lonza Biologics, Inc.; Vacaville (CA); On-site; Confidential; Full time

Benefits offered by this job

Performance-related bonus

Medical, dental and vision insurance

401(k) matching plan

Life insurance

Short-term and long-term disability

Employee assistance programs

Paid Time Off

Job summary

Lonza Biologics, Inc. in Vacaville is seeking a shift leader to manage the manufacturing shift and drive performance, quality, and compliance. The role requires in-person leadership to support real-time collaboration and high precision in medicines manufacturing.

You will lead a team, ensure cGMP adherence, and coordinate lean initiatives and improvements while maintaining inspection readiness and health authority compliance.

Qualifications

• 5–6 years of supervisory experience in biotech, pharmaceutical, or related industries.
• AS/BS/BA in Biological Sciences, Physical Sciences, or Engineering preferred.
• 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.
• Demonstrated ability to drive quality and productivity improvements via Lean and other CI methods.

Responsibilities

• Accountable for manufacturing shift performance, including budget management, productivity, labor efficiency, and achievement of operational goals.
• Ensure cGMP compliance and inspection readiness for site at all times; actively support inspection activities.
• Ensure production of high-quality products in accordance with Health Authority regulations and Lonza quality systems.
• Drive Lean manufacturing and continuous improvement initiatives to enhance efficiency, quality, and operational performance.
• Lead, train, and develop manufacturing staff to ensure qualification, accountability, and high team performance.
• Oversee manufacturing equipment, facilities, and validated processes, coordinating maintenance and technical improvements as needed.
• Manage deviations, investigations, validation strategies, and technical transfers while implementing sustainable corrective and preventive actions.

Skills

Supervisory experience

Lean manufacturing

cGMP compliance

Inspection readiness

Bioprocessing tech

Education

AS/BS/BA in Biological Sciences or Engineering

Job description

Location: Vacaville, California

This is a fully site based role. Working together in person supports close, real time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.

Shift leader will foster an environment founded on trust, accountability, and mutual respect and will provide active, visible leadership to maintain and enhance the company's position as a best-in-class, bio-pharmaceutical manufacturer.

What you will get

The full-time base annual salary for this position is expected to range between $95,250 to $158,750. In addition, below you will find a comprehensive summary of the benefits package we offer:

• Performance-related bonus

• Medical, dental and vision insurance

• 401(k) matching plan

• Life insurance, as well as short-term and long-term disability insurance

• Employee assistance programs

• Paid Time Off

Shift hours: 6:30pm-7:30am; Wednesday-Friday and every other Saturday

What you will do

• Accountable for manufacturing shift performance, including budget management, productivity, labor efficiency, and achievement of operational goals.

• Ensure cGMP compliance and inspection readiness for site at all times. Actively support inspection activities.

• Ensure production of high-quality products in accordance with Health Authority regulations and Lonza quality systems.

• Drive Lean manufacturing and continuous improvement initiatives to enhance efficiency, quality, and operational performance.

• Lead, train, and develop manufacturing staff to ensure qualification, accountability, and high team performance.

• Oversee manufacturing equipment, facilities, and validated processes, coordinating maintenance and technical improvements as needed.

• Manage deviations, investigations, validation strategies, and technical transfers while implementing sustainable corrective and preventive actions.

What we are looking for

• AS/BS/BA in Biological Sciences, Physical Sciences, or Engineering preferred.

• Minimum 5-6 years of supervisory experience in a biotech, pharmaceutical, or related industry preferred.

• Proven track record of ensuring safe, compliant, and efficient operations in a large-scale cGMP manufacturing environment.

• Proven success in leading cGMP-compliant operations through health authority inspections, with a background in aseptic and bioprocessing technologies preferred.

• Shown ability to drive quality and productivity improvements through the use of Lean and other continuous improvement methods.

• Ability to lead/guide/develop an operational staff team to achieve beneficial results in a dynamic environment.

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law.