Biotechnologist Level 2 (Nights)

Lonza, Inc.•Portsmouth, NH

47d•Onsite

About The Position

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising 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 to be part of. Be at the cutting-edge of innovation and technology and make a difference from day one. In a role at Lonza as a Manufacturing Associate, you could help positively impact people's lives all around the world. 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. Check out more about what a life at Lonza in Portsmouth, NH could look like for you. Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising 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: From 7pm-7am on a rotating schedule each week: Week 1: Mon, Tues, Fri, Sat, Sun Week 2: Wed, Thurs Shift differentials are included 4 Hours of overtime built into your schedule each week

Requirements

High School Diploma or equivalent minimum with an AS/BS preferred
Preferred area of study: Science related discipline, degrees in Genetics are relevant.
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.

Responsibilities

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.