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 dedicated 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!
We are seeking a Biotechnologist II to join our team in Portsmouth, NH. This full-time, on-site role supports day shift operations (7 AM – 7 PM) on a rotational schedule. The ideal candidate will be a skilled and dedicated individual responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. It also requires a strong understanding of cGMP compliance and aseptic techniques.
Schedule
Rotational: 2 on, 2 off, 3 on, 2 off, 2 on, 3 off (repeat)
Day Shift: 7:00 AM – 7:00 PM
Weekend shifts include additional pay.
Key Responsibilities
Process Operations & Monitoring: Execute process recipes and SOPs to set up, operate, and monitor equipment, including Clean-in-Place (CIP) and Steam-in-Place (SIP) operations.
Documentation & Quality: Report production activities in written and electronic documents in accordance with Good Manufacturing Practices (GMPs) and Good Documentation Procedures (GDPs), and review batch records and logbooks.
Laboratory & Aseptic Techniques: Independently perform laboratory tasks such as pH and conductivity testing and product sampling, while demonstrating proficient aseptic technique.
Troubleshooting & Deviation Management: Troubleshoot equipment events and initiate deviations as appropriate to maintain process integrity.
Facility & Material Handling: Perform routine cleaning and sanitization tasks to maintain the facility and equipment, support 6S programs, and manage raw material and chemical transfers.
Training & Professional Development: Attain and maintain qualification for all assigned tasks, and with strong communication skills, may be asked to train Level I Associates on specific procedures.
Qualifications
1-2 years of experience in a Biotech or Pharmaceutical production/manufacturing environment.
Related experience in a lab or other GMP-compliant biotech setting may be considered.
Strong understanding of cGMP regulations and aseptic techniques.
Proficiency in laboratory tasks such as pH and conductivity testing.
Excellent attention to detail and strong documentation skills.
Ability to work effectively both independently and as part of a team.
Reporting Structure
Reports to a Shift Supervisor.
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.