MSAT Senior Scientist, Analytical Development Services Full-time

MSAT Scientist II, Analytical Development Services

Location: 100% on-site. Portsmouth, NH.

The MSAT Scientist II, Analytical Development Services (ADS) incumbent is responsible for performing Analytical Development activities including assay work, result interpretation and instrument troubleshooting, with minimal supervisory direction. The individual performs a variety of routine and non-routine work within established policies and procedures and receives detailed instructions on new projects and assignments.

What you will get:

• A collaborative and inclusive work environment.
• Opportunities for career growth and development.
• Access to cutting-edge technologies and tools.
• Competitive compensation and benefits package.
• Supportive leadership and mentoring.
• Commitment to ethical and sustainable practices.

What you will do:

• Perform routine analytical assays following standardized SOPs
• Train on more advanced methodologies and be involved in analytical method transfers
• Analyze data sets, draw conclusions, and prepare slides to present findings at group meetings.
• Maintain lab housekeeping and safety audits (6S activities), monitor preventative maintenance and periodically review documents.
• Represent the lab on internal and external project teams, provide progress updates, and participate in customer call decision-making.
• Ensure all mandatory cGMP requirements and training profiles (e.g., ComplianceWire, Cornerstone) remain up to date at all times.

What We Are Looking For:

• Minimum of Bachelor of Science degree required, preferred in Biotechnology area, Biological Sciences, or Chemical Engineering. Typically requires 3+ years of relevant experience.
• Strong communication skills. Able to clearly express ideas and point of view both verbally and in writing. Has good interpersonal skills. Shows commitment and dedication and strives to be ahead of schedule.
• Able to shift priorities based on company needs and able to multitask on multiple projects.
• Ability to think critically and logically.
• In depth knowledge of large scale manufacturing, current Good Manufacturing Practices (cGMP) and US/EU regulations.
• Working experience with data analysis.

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.