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Quality Control Supervisor Construction Jobs (NOW HIRING)

QC Supervisor - Microbiology Location: Portsmouth, NH Day Shift: Monday-Friday, 8:00 AM-4:30 PM We are seeking a QC Supervisor - Microbiology to lead a team of Quality Control professionals ...

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Quality Control Supervisor Construction information

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How much do quality control supervisor construction jobs pay per year?

As of Sep 11, 2026, the average yearly pay for quality control supervisor construction in the United States is $98,073.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,500.00 and $111,000.00 per year, depending on experience, location, and employer.

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Infographic showing various Quality Control Supervisor Construction job openings in the United States as of June 2026, with employment types broken down into 67% Full Time, 30% Part Time, and 3% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $98,073 per year, or $47.2 per hour.

QC Supervisor (Day Shift)

Portsmouth, NH • On-site

Lonza
Biotechnology Research and Development • 10K+ employees

Full-time

Medical, Dental, Vision

Re-posted 2 days ago


Key responsibilities

  • Lead and develop a team of QC analysts performing microbiological testing in a GMP-regulated environment.

  • Plan, prioritize, and coordinate testing activities to support manufacturing schedules, product release, and customer commitments.

  • Review and approve laboratory documentation while ensuring compliance with GMP and regulatory requirements.


Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz


Job description

QC Supervisor - Microbiology

Location: Portsmouth, NH

Day Shift: Monday-Friday, 8:00 AM-4:30 PM

We are seeking a QC Supervisor - Microbiology to lead a team of Quality Control professionals supporting microbiological testing activities at our Portsmouth, NH site. In this role, you will provide leadership, direction, and development to a team responsible for supporting product quality, regulatory compliance, and operational excellence. This is an exciting opportunity for a people-focused leader who is passionate about quality, continuous improvement, and developing high-performing teams.

What you will get

  • An agile career and dynamic working culture.

  • An inclusive and ethical workplace.

  • Compensation programs that recognize high performance.

  • Medical, dental, and vision insurance.

  • Opportunities for career growth and professional development.

  • Meaningful work supporting therapies that improve patient lives.

  • A collaborative environment focused on innovation, safety, and quality.

What you will do

  • Lead and develop a team of QC analysts performing microbiological testing in a GMP-regulated environment.

  • Ensure laboratory activities support manufacturing schedules, product release, and customer commitments.

  • Plan, prioritize, and coordinate testing activities to achieve quality and operational goals.

  • Review and approve laboratory documentation while ensuring compliance with GMP and regulatory requirements.

  • Drive accountability, performance, and professional development through coaching and mentoring.

  • Lead process improvement initiatives that enhance laboratory effectiveness, compliance, and efficiency.

  • Collaborate with Quality Assurance, Manufacturing, and site stakeholders to resolve issues and support business objectives.

What we are looking for

  • Bachelor's degree in Microbiology, Biology, Life Sciences, or a related scientific discipline.

  • Experience working in a Quality Control laboratory within a GMP-regulated environment.

  • Strong Microbiology experience; Environmental Monitoring experience is preferred.

  • Previous supervisory or people management experience with a proven ability to lead teams.

  • Strong performance management skills, including coaching, mentoring, and accountability.

  • Experience supporting or leading process improvement and continuous improvement initiatives.

  • Excellent organizational, communication, and problem-solving skills.

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. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.


What Lonza employees say

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About Lonza

Sourced by ZipRecruiter

Industry

Biotechnology research and development and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Bern, KS, US