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Manufacturing Supervisor

Lonza · Portsmouth, NH

Apply on Lonza ↗
Level
Supervisor
Team
Manufacturing
Degree
Required
Industry
Pharma & life sciences
Posted
11 days ago

The role in 30 seconds

A supervisor manufacturing role at Lonza (pharma & life sciences) in Portsmouth, NH. You will lead a team responsible for producing therapeutic proteins in a highly regulated cGMP environment.

They ask for
degree required
Tools it names
FDA / GMP

Read from the posting. The full description is below.

From the plant jobs report · week of October 19, 2026

Production Supervisor roles in the US: typical posted base $76k–$102k.

Median of the low and high ends of 249 live postings that list pay, out of 928 production supervisor openings in the US, read from manufacturers' own careers sites.

New Hampshire plant jobs report →Pay by team and state →What moves pay →

How this role compares

Against 16 other live manufacturing postings in New Hampshire.

Experience asked
Not stated

Similar roles usually ask 4+ years.

Skills these teams ask for most

  • ✓ Team leadership 76%
  • ✓ FDA / GMP 65%
  • Validation (IQ/OQ/PQ) 47%
  • CNC 24%

✓ = this posting asks for it too. % = share of similar postings that mention it.

At a glance

Pulled from the posting text. If it's not listed here, the posting didn't say.

How to get in at this plant

Five moves over a week or two. The first one takes ten minutes.

  1. 1

    Pick 2–3 people on the Manufacturing team at Lonza

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  2. 2

    Send a short, curious note

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  3. 3

    Turn a reply into a short call

    Questions worth asking about this team:

    • What does a normal week look like on your team?
    • Is the work mostly new product launches or sustaining existing lines?
    • How much time do you spend on the floor versus at a desk?
    • How did you land the job? What stood out in your interviews?
  4. 4

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    If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.

  5. 5

    Bring proof to the interview

    One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.

This plant: Lonza in Portsmouth

16 other open roles at this site · 1 person we found in manufacturing roles at Lonza.

All 17 roles at Lonza →
Full description from LonzaAs posted on their careers site.Show

What you will do

  • ◆Lead daily manufacturing operations to ensure safe, compliant, and on-time execution of the production schedule
  • ◆Coach, train, and develop operators through performance management, career planning, and ongoing development activities
  • ◆Monitor manufacturing activities to ensure compliance with cGMP requirements, quality systems, SOPs, and safety standards
  • ◆Review batch records, logbooks, and production documentation to support timely batch release with minimal errors
  • ◆Coordinate activities across multiple departments to troubleshoot equipment and process-related issues
  • ◆Support recruiting, onboarding, staffing, and workforce planning activities
  • ◆Drive continuous improvement initiatives while maintaining inspection readiness and operational excellence
Show full description ↓

Manufacturing Supervisor

Location: Portsmouth, NH (On-site)

At Lonza, our greatest scientific solution is talented people working together to help improve lives around the world. As a Manufacturing Supervisor, you will lead a team responsible for producing therapeutic proteins in a highly regulated cGMP environment. Your leadership will help ensure safe, compliant, and efficient manufacturing operations while supporting the delivery of life-changing therapies to patients worldwide.

This is an exciting opportunity for a manufacturing leader who enjoys developing people, driving operational excellence, and solving complex challenges in a fast-paced biotechnology environment. You'll play a key role in production planning, team development, compliance oversight, and continuous improvement initiatives while partnering closely with Manufacturing, Engineering, MSAT, Scheduling, and other support functions.

Shift: Rotating 12-hour day shifts (7:00 AM–7:00 PM) on an alternating 2-2-3 schedule.

What you will get

  • •An agile career and dynamic working culture
  • •Opportunities to lead, coach, and develop a high-performing manufacturing team
  • •Exposure to advanced biologics manufacturing processes and technologies
  • •A collaborative environment with cross-functional partners across the site
  • •Compensation programs that recognize high performance
  • •Medical, dental, and vision insurance
  • •Opportunities for career growth and leadership development

What we are looking for

  • •Associate's or Bachelor's degree in a science-related discipline, or a high school diploma/equivalent with relevant experience
  • •Manufacturing experience in a cGMP-regulated environment
  • •Previous supervisory or team leadership experience preferred
  • •Strong understanding of quality systems, GMP compliance, and manufacturing operations
  • •Excellent communication, problem-solving, decision-making, and organizational skills
  • •Experience leading employees through training, coaching, and performance development
  • •Ability to work cross-functionally and effectively manage multiple priorities in a dynamic production 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. 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.

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