MSAT Development Services Scientist I

Lonza Group Ltd.; Vacaville (CA); On-site; USD 70,000 - 116,000; Full time

Benefits offered by this job

Performance bonus

Medical insurance

Dental insurance

Vision insurance

401(k) matching

Life insurance

Disability insurance

Employee assistance program

Paid Time Off

Job summary

Lonza Vacaville site-based role in Development Services. The Scientist I performs downstream purification process activities under supervision, including lab studies and analytical assays, while applying technical knowledge and seeking guidance when needed.

Responsibilities include running routine studies, data analysis, study protocol drafting, and supporting tech transfer with documentation and communication to teams. A BS in Biological Sciences, Biomedical, or Chemical Engineering is required.

Qualifications

• Bachelor of Science degree required in Biological Sciences, Biomedical, Chemical Engineering.
• Learns quickly and adapts to change.
• Takes responsibility for mistakes and uses them as opportunities to improve.
• Works well with others and shares knowledge.

Responsibilities

• Execute routine downstream process development studies and laboratory experiments under supervision.
• Perform routine analytical testing and maintain proficiency in downstream assays.
• Serve as Study Director for simple studies with timely execution and documentation.
• Analyze data, interpret results, and support process development decisions.
• Draft study protocols, reports, and presentations; communicate findings to team.

Education

Bachelor of Science degree in Biological Sciences, Biomedical, Chemical Engineering

Job description

Location: Vacaville, California This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.

Development Services Scientist I performs downstream purification process activities under supervisory guidance, including laboratory studies and analytical assay execution. Performs routine work following established procedures, receives direction on new assignments, and applies technical knowledge to complete tasks while seeking guidance when additional clarification or expertise is needed.

What you will get

The full-time base annual salary for this position is expected to range between $69,750 to $116,250.

In addition, below you will find a comprehensive summary of the benefits package we offer:

• Performance-related bonus
• Medical, dental and vision insurance
• 401(k) matching plan
• Life insurance, as well as short-term and long-term disability insurance
• Employee assistance programs
• Paid Time Off

What you will do

• Execute routine downstream process development studies and laboratory experiments in accordance with SOPs, with guidance from senior scientists.
• Perform routine analytical testing and maintain proficiency in relevant downstream analytical assays.
• Serve as Study Director for simple studies, ensuring timely execution, documentation, and communication of results.
• Analyze experimental data, interpret results, and draw sound scientific conclusions to support process development decisions.
• Draft study protocols, reports, and technical presentations, and communicate findings at team and project meetings.
• Support technology transfer activities, satellite runs, buffer/stability studies, and other routine downstream process investigations.
• Maintain laboratory compliance through equipment maintenance, documentation review, safety audits, training completion, and adherence to cGMP and quality requirements.

What we look for

• Bachelor of Science degree in the field of Biological Sciences, Biomedical, Chemical Engineering
• Learns quickly, adapts to change, and is open to new ways of working.
• Takes responsibility for mistakes and uses them as opportunities to improve.
• Works well with others, shares knowledge, and values different perspectives.
• Delivers high-quality results on time and stays focused on goals.
• Understand customer needs and takes action to provide good support and service.
• Shows ownership, accountability, and a strong commitment to safety and compliance.

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.

Ready to shape the future of life sciences?