Biotechnologist I

Lonza•Portsmouth, NH

3d•Onsite

About The Position

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).

Requirements

High school diploma or equivalent required
Basic computer skills, including Microsoft Office
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

Nice To Haves

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

Responsibilities

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