Biotechnologist I (Nights - A Shift)

Lonza Biologics, Inc.; Portsmouth (VA); On-site; Confidential; Full time

Benefits offered by this job

Agile culture

Inclusive workplace

Competitive compensation programs

Medical, dental, and vision insurance

Career growth opportunities

Collaborative team environment

Job summary

Lonza Biologics, Inc. in Portsmouth, NH, is seeking a Biotechnologist I to support production of therapeutic proteins in a GMP setting. You will operate equipment, perform downstream purification, and assist in safe, high-quality manufacturing.

The role includes shift work on a 12-hour cycle with two on/off patterns. Ideal candidates have a science background and hands-on biopharma experience, with strong attention to detail and teamwork.

Qualifications

• High school diploma or equivalent required; AS/BS preferred.
• Experience in biopharmaceutical manufacturing or regulated production preferred.
• Experience with downstream purification processes or chromatography preferred.

Responsibilities

• Set up, operate, and monitor manufacturing equipment including purification systems.
• Execute downstream manufacturing operations such as chromatography and filtration.
• Support column packing and viral reduction filtration activities.
• Perform laboratory tasks like pH 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 assist with documentation reviews.
• Participate in shift handovers and team improvement initiatives.

Skills

Hands-on bioscience

Problem solving

Teamwork

Attention to detail

Education

High school diploma or equivalent

AS/BS in a science-related field preferred

Tools

Microsoft Office

Job description

Job Title: Biotechnologist I

Location: Portsmouth, NH, USA

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. Working in a GMP manufacturing environment, you will operate production equipment, execute downstream purification processes, and ensure products are manufactured safely and to the highest quality standards. This role is ideal for someone with an interest in biomanufacturing who enjoys hands-on operations, problem-solving, and working as part of a collaborative team

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

• 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 manufacturing equipment, including purification systems, CIP, and SIP processes


• Execute downstream manufacturing operations, including chromatography, filtration, and product processing activities


• Support column packing, viral reduction filtration, and other purification-related operations


• 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, team 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 biopharmaceutical manufacturing, biotechnology, or regulated production environments preferred


• Experience with downstream purification processes, chromatography operations, or filtration systems preferred


• Column packing and viral reduction filtration experience is highly desirable


• Strong attention to detail and ability to follow procedures accurately


• Good written and verbal communication skills


• Ability to work effectively 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, 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.