QC Scientist I-Technical Transfer (Biotech)
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 to be part of.
Lonza AG is thrilled to offer an outstanding opportunity for a Quality Control Scientist 1- Technical Transfer in our New Hampshire, USA location! This role plays a crucial role in our ambitious journey to uphold and improve our world-class standards in life sciences. As a member of our dedicated Quality Control team, you will directly contribute to technology transfer, validation, deviation support, routine testing, and investigation projects. This role is crafted for someone who excels in a collaborative environment and is dedicated to scientific excellence.
Key responsibilities:
Perform assay work for transfers, validations, investigations, and routine testing
Perform sophisticated laboratory work as the Subject Matter Expert in one or more fields
Lead document writing for transfers, validations, and investigations, including test methods, protocols, and reports
Ensure detailed execution post technical transfer by training personnel, reviewing data, and completing documentation
Set up and verify electronic equipment, templates, and forms for transfers and validations
Apply Data Integrity principles strictly in compliance with Lonza DI policies, guidelines, and procedures
Participate actively in project team meetings to determine and drive project success
Independently drive assigned projects to successful and timely completion
Provide mentorship and training to junior staff to achieve goals in accordance with established policies
Act as an advisor to junior staff to meet schedules and resolve technical problems
Perform other duties as assigned
Key requirements:
Bachelor's degree required; Advanced Graduate Degree (MS/PhD) preferred
A combination of education and years of experience will be considered
Preferred 5+ years in a GMP/Professional environment; 0-4 years of experience also considered
Proven track record to work collaboratively in a team environment
Outstanding technical writing skills for regulatory documents
Effective communication skills for direct customer and project team interactions
Join us in our mission to devise innovative solutions that help businesses and improve lives. Apply today to become a part of Lonza AG's dynamic and ambitious team.
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.
