Biotechnologist I - (Nights)

US02 Lonza Biologics Inc.; Portsmouth (NH); On-site; USD 60,000 - 78,000; Full time

Benefits offered by this job

Night shift differential

Health insurance

Dental insurance

Vision insurance

Career development

Collaborative environment

Equal opportunity employer

Job summary

Lonza Group Ltd. in Portsmouth, NH is seeking a Biotechnologist I to support the production of therapeutic proteins on a 12-hour night shift. You will operate equipment, follow SOPs, and perform lab tasks including pH and conductivity testing to ensure high-quality medicines.

The role is onsite with benefits including health coverage, career development, and a collaborative team environment. You will participate in continuous improvement and shift handovers to maintain safe, compliant production.

Qualifications

• High school diploma or equivalent required; AS or BS in a science-related field preferred.
• Experience in manufacturing or regulated environments; GMP experience preferred.
• Strong attention to detail and ability to follow procedures accurately.
• Good communication skills, both written and verbal.
• Ability to follow procedures in a regulated environment.
• Ability to work in a team environment and adapt to changing priorities.
• Basic computer skills, including Microsoft Office.

Responsibilities

• Set up, operate, and monitor production equipment, including CIP and SIP processes.
• Execute manufacturing processes by following SOPs and good documentation practices.
• Perform laboratory tasks such as pH testing, conductivity testing, and product sampling.
• Move and transfer materials across production areas safely and accurately.
• Maintain equipment and facilities through routine cleaning and sanitization.
• Troubleshoot basic equipment issues and support documentation review.
• Participate in shift handovers, meetings, and continuous improvement activities.

Job description

Job Title: Biotechnologist I (Nights) Location: Portsmouth, NH As a Biotechnologist I at our Portsmouth site, you will support the production of therapeutic proteins that help improve the lives of patients around the world. You will work as part of a team to operate equipment, follow procedures, and ensure products are manufactured safely and to the highest quality standards. This role is based onsite, where working in person supports collaboration and the precision needed to manufacture medicines to the highest quality and safety standards. This role follows a 12-hour day shift schedule from 7:00 PM to 7:00 AM on a rotating schedule of alternating days: two on, two off, three on, two off, two on, three off (repeating cycle).

What you will get

• Pay differential for Night and Weekend shifts
• An agile career and dynamic working culture
• An inclusive and ethical workplace
• Compensation programs that recognize high performance
• Medical, dental, and vision insurance
• Opportunities to grow and develop your career
• A collaborative and supportive team environment

What you will do

• Set up, operate, and monitor production equipment, including CIP and SIP processes
• Execute manufacturing processes by following SOPs and good documentation practices
• Perform laboratory tasks such as pH testing, conductivity testing, and product sampling
• Move and transfer materials across production areas safely and accurately
• Maintain equipment and facilities through routine cleaning and sanitization
• Troubleshoot basic equipment issues and support documentation review
• Participate in shift handovers, meetings, and continuous improvement activities

What we are looking for

• High school diploma or equivalent required; AS or BS in a science-related field preferred
• Experience in manufacturing or regulated environments; GMP experience preferred
• Strong attention to detail and ability to follow procedures accurately
• Good communication skills, both written and verbal
• Ability to follow procedures in a regulated environment
• Ability to work in a team environment and adapt to changing priorities
• Basic computer skills, including Microsoft Office

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, colour, 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.

Every day, our teams across the world work together to turn scientific breakthroughs into life-changing medicines that reach up to 100 million patients a year.

Lonza is a place where people can make a unique impact, grow their careers and belong.

You will feel at home at Lonza if you:

• Take ownership, step forward, and enjoy meaningful responsibility
• Love solving problems and thrive in a complex, fast-moving environment
• Are curious, always looking to learn and improve
• Work collaboratively, contributing to something bigger than yourself
• Are motivated to make a difference through work that impacts customers and their patients

Why Lonza: We are a place of unique opportunity, where your ideas, expertise and ambition can make a real difference. Here, you will have the freedom to grow, the support to succeed and the chance to contribute to work that matters. We are the makers of the medicines of tomorrow. Join us. Be you.