Manufacturing Associate level 2 - Nights

Lonza•Portsmouth, NH

1d•Onsite

About The Position

As a Manufacturing Associate II, you will support the production of therapeutic proteins in a cGMP manufacturing environment, operating equipment, performing laboratory testing, and executing production processes that help deliver life-changing therapies to patients. This hands-on role requires strong attention to detail, problem-solving skills, and a commitment to quality, safety, and continuous improvement. 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
Manufacturing experience preferred
Experience working in upstream and/or downstream manufacturing environments preferred
Strong problem-solving, critical thinking, and decision-making skills
Ability to follow procedures and maintain accurate documentation
Strong written and verbal communication skills
Ability to work a rotating 12-hour day shift schedule in a team-based manufacturing environment

Nice To Haves

Associate's or Bachelor's degree in a science-related field preferred
cGMP or biopharmaceutical experience is a plus

Responsibilities

Operate manufacturing equipment and execute downstream production processes in accordance with cGMP requirements
Set up, monitor, and support process equipment, including Clean-in-Place (CIP) and Steam-in-Place (SIP) operations
Perform laboratory activities, including pH testing, conductivity testing, and product sampling
Transfer materials and chemicals safely throughout manufacturing areas
Complete production documentation, batch records, and electronic records following Good Documentation Practices (GDP)
Support equipment troubleshooting, routine sanitization activities, and 6S initiatives
Participate in shift handovers, team meetings, training activities, and continuous improvement projects