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.
Job Description:
At Lonza, the Biotechnologist Level I (Nights) assumes a meaningful role in the manufacturing of therapeutic proteins (API) under cGMP conditions. This outstanding opportunity enables you to be part of a world-class team, working nights from 7pm-7am on a rotational schedule.
Week 1: M/T/F/SAT/SUN
Week 2: W/TH
We are seeking dedicated individuals who are prepared to tackle the challenge of upholding our high standards and contributing to our mission with outstanding precision! As a Biotechnologist Level I, you will:
Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations. You will report production in written and electronic documents in accordance with good manufacturing practices (GMPs) and good documentation procedures (GDPs), and review documentation as appropriate.
Attain qualification for all assigned tasks and maintain an individual training plan to ensure continuous improvement and compliance.
Perform basic laboratory tasks, such as monitoring pH, conductivity, and testing product samples to ensure the quality and consistency of our products.
Complete material movements, transferring raw materials and chemicals into, out of, and across the production areas with strict adherence to safety protocols.
Maintain the facility and equipment through routine cleaning and sanitization, supporting our 6S programs to uphold our dedication to a clean and organized workspace.
Complete administrative tasks including attending shift exchanges, meetings, sending/receiving emails, and participating in projects to support the overall efficiency and success of the team.
Perform other duties as assigned to meet the dynamic needs of our production environment.
Key Requirements:
To succeed in this role, you must possess the following qualifications:
A minimum of a High School Diploma or equivalent experience; an AS/BS degree or equivalent experience is preferred.
Proven logic and decision-making abilities, with strong critical thinking skills that enable you to troubleshoot and resolve issues effectively.
Strong written and verbal communication skills are essential for clear and accurate reporting and collaboration.
Manufacturing experience necessary, preference for cGMP or Associate Level I bio-pharma experience.
At Lonza, we are dedicated to crafting an inclusive environment where every team member can thrive. We promote collaboration and value the outstanding contributions of each individual. Join our team and help us successfully implement ambitious projects that make a difference in the world!
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.