Lonza America Inc

MSAT Development Services Scientist I

Lonza America Inc • $69K — $116K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor of Science degree in Biological Sciences, Biomedical, or Chemical Engineering.
  • Quick learner who adapts to change and new methodologies.
  • Responsible and reflective, using mistakes as learning opportunities.
  • Team-oriented, sharing knowledge and valuing diverse perspectives.
  • Focuses on delivering high-quality results promptly and efficiently.
  • Customer-focused, taking proactive steps to support and meet needs.
  • Demonstrates ownership and a strong commitment to safety and compliance.

Responsibilities

  • Execute routine downstream process development studies and experiments following SOPs with guidance.
  • Perform routine analytical testing and maintain proficiency in analytical assays relevant to downstream processes.
  • Act as Study Director for straightforward studies, managing execution and communication of results.
  • Analyze experimental data to support process development decisions based on sound scientific conclusions.
  • Draft study protocols, reports, and technical presentations, communicating findings in team meetings.
  • Support technology transfer activities and routine downstream process investigations like buffer/stability studies.
  • Ensure laboratory compliance through equipment maintenance, documentation, audits, and adherence to cGMP standards.

Benefits

  • Performance-related bonus
  • Medical, dental, and vision insurance
  • 401(k) matching plan
  • Life insurance and both short-term and long-term disability insurance
  • Employee assistance programs
  • Paid Time Off
Full 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.
  • Understands customer needs and takes action to provide good support and service.
  • Shows ownership, accountability, and a strong commitment to safety and compliance.


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

About Lonza America Inc

Lonza America Inc is a subsidiary of Lonza Group, a Swiss multinational company that provides products and services to the pharmaceutical, biotech, and specialty ingredients markets. Lonza America Inc is responsible for the North American market and offers a range of products and services, including custom manufacturing, research and development, and quality control testing. The company has a strong focus on sustainability and has implemented various initiatives to reduce its environmental impact. Lonza America Inc was founded in 1897 and has since grown to become a leading provider of products and services in the pharmaceutical and biotech industries.
Learn more about Lonza America Inc
Size
16,218 employees
Industry
NASDAQ

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