What are the responsibilities and job description for the Manufacturing Associate position at Lonza?
Be at the cutting-edge of innovation and technology and make a difference from day one as a Manufacturing Associate at Lonza.
You could help positively impact people's lives all around the world by working with us.
See Pharma from new angles, experience new opportunities, and work in a dynamic culture
At our global hub in Portsmouth, NH, you'll be surrounded by the best minds in the business making a meaningful difference for millions.
About Us
Today, Lonza is a global leader in life sciences operating across five continents.
We operate without a magic formula, instead relying on talented people working together to devise ideas that help businesses to help people.
In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want you to be part of.
Shift Schedule
Work from 7pm-7am on a rotating schedule each week:
- Week 1: Monday, Tuesday, Friday, Saturday, Sunday
- Week 2: Wednesday, Thursday
- Shift differentials are included for weekends worked
- 8 hours of overtime built into your schedule each week
What You'll Get
- An initial two-week training period on day shift Monday-Friday upon hire
- An agile career and dynamic working culture
- An inclusive and ethical workplace
- Compensation programs that recognize high performance
- A variety of benefits dependent on role and location
What You'll Do
- Provide a safe, controlled work environment in all areas of expertise. Be aware of the site safety objectives and make sure they are communicated and understood.
- Work with customer subject matter experts to transfer in and maintain customers' processes in the production facility.
- Provide effective training for manufacturing staff related to any new equipment or systems to be used in Cell Therapy (CT).
- Collaborate with the CT Manufacturing Leadership team to incorporate process and operational improvements.
- Support building and establishing the manufacturing team.
- Author, review, and approve documentation.
What We're Looking For
- A high school diploma or equivalent minimum with an associate's degree or bachelor's degree preferred.
- Prior work experience in a cleanroom, laboratory, or another sterile setting is preferred.
- Prior experience with Aseptic Techniques and gowning procedures is preferred.
- Working experience in manufacturing; cGMP setting preferred. The ideal candidate will have experience within the Cell and Gene Therapy field.
- Able to follow documentation procedures for day-to-day tasks in a regulated industry.
- Proven logic and decision-making abilities, critical thinking skills.
- Strong written and verbal communication skills.
Why Work with Us
Every day, Lonza's products and services have a positive impact on millions of people.
We respect and protect our people and our environment.
Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences.
We offer the satisfaction that comes with improving lives all around the world.
The satisfaction that comes with making a meaningful difference.
