Biotechnologist I (Nights - B Shift)
Lonza
Summary
Level I associates have the remarkable opportunity to be part of a high-reaching team at Lonza, where world-class biotechnological solutions come to life. Our Biotechnologist I role is essential to our manufacturing operations in New Hampshire, USA. This position is ideal for those who strive to deliver outstanding performance and are passionate about making a difference in the life sciences field.
Job description
This position is for the night shift from 7pm-7am, on a rotational schedule every other week:
- Week 1: M/T - F/SAT/SUN
- Week 2: W/TH
- Shift differentials are included for weekends and nights worked
Key Responsibilities
- Operate and maintain equipment, supervise production processes, and meticulously report production in both written and electronic formats. Follow GMPs and GDPs, troubleshoot issues, and review documentation to ensure strict compliance.
- Exhibit expertise in suite-specific production activities and laboratory tasks such as bioreactor inoculation and chromatography column operation. Understand and apply the scientific theories behind these processes. You may also be responsible for training other associates on these tasks and theories.
- Run administrative tasks, including attending shift exchanges, participating in meetings, sending and receiving emails, and engaging in projects. In addition, you will be involved in technical writing, such as documenting deviations and completing document change forms.
- Attain and maintain qualification for all assigned tasks and adhere to an individual training plan to ensure continuous improvement and compliance.
- Perform material movements, including the transfer of raw materials and chemicals into, out of, and across production areas. Other duties may be assigned as needed.
Key Requirements/Preferences
- High School Diploma or equivalent experience required; AS/BS in a Scientific Field preferred.
- Confirmed working experience in manufacturing, preferably in a cGMP setting, or some experience as an Associate Level I in the bio-pharma industry.
- Demonstrated logical decision-making abilities, critical thinking skills, and strong written and verbal communication skills.
- Flexibility to adapt to changing business priorities, live the cultural beliefs, and actively seek and implement feedback to improve performance.
Requirements
- High School Diploma or equivalent experience required
- AS/BS in a Scientific Field preferred
- Confirmed working experience in manufacturing, preferably in a cGMP setting, or some experience as an Associate Level I in the bio-pharma industry
- Demonstrated logical decision-making abilities, critical thinking skills, and strong written and verbal communication skills
- Flexibility to adapt to changing business priorities, live the cultural beliefs, and actively seek and implement feedback to improve performance
Benefits
- Shift Differentials
Company overview
Lonza is a pioneering global Contract Development and Manufacturing Organization (CDMO) and a world leader in pharmaceutical manufacturing services. Founded in 1897 in Switzerland, the company has evolved into the first and original CDMO, now operating as one of the largest Western CDMO networks with approximately 19,000 employees across more than 30 sites spanning five continents. Lonza specializes in transforming therapeutic discoveries into life-saving and life-enhancing treatments for patients worldwide. The company's comprehensive services span from early development to drug substance and drug product manufacturing, covering established and emerging technologies including mammalian biologics, small molecules, highly potent APIs, bioconjugates, mRNA, microbial products, and cell and gene therapies. With a focus on cutting-edge science, smart technology, and lean manufacturing, Lonza serves a diverse customer base ranging from emerging biotechs to global pharmaceutical companies, delivering integrated solutions throughout the entire treatment lifecycle.