Biotechnologist I (Nights - B Shift)

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 crucial to our manufacturing operations in Portsmouth, New Hampshire. This position is ideal for those who strive to deliver outstanding performance and are passionate about making a difference in the life sciences field! 

This position is for the night shift from 7pm-7am, on a rotational schedule every other week:

• Week 1: M/T , F/SAT

• Week 2: SUN/W/TH

• Shift differentials are included for nights and weekends worked 

Check out this video on what it’s like to work at Lonza, Portsmouth, NH: https://www.youtube.com/watch?v=US5Lelszx9Q&list=PLh3u2rKfWyIfXC2d2O3enUrpMjjJ7DO_x&index=22

Grow your career with a global leader in pharmaceutical manufacturing!

What you will get:

• An agile career and dynamic working culture.

• An inclusive and ethical workplace.

• Compensation programs that recognize high performance.

• Medical, dental and vision insurance, 401(k) plan and company match.

• Paid Time Off and paid holidays.

• Annual bonus opportunity.

• Continuous Learning and Career Development opportunities.

• And much more

Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits.

What you will do:

• 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. 

What we are looking for:

• 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. 

About Lonza:

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.