Lonza

Research Scientist III

United States · Work style not stated · Full time

Apply on the employer’s site ↗See how well you match this job

You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.

About the role

Description from the employer’s posting. Check the employer’s page for the current version.

  • EmployerLonza
  • LocationUnited States
  • Work styleWork style not stated
  • Employment typeFull time
  • Employer posted

Research Scientist III

Tampa, FL

The actual location of this job is in Tampa, Florida, US. Relocation assistance is available for eligible candidates and their families, if needed.

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.

What you will get:

  • An agile career and dynamic working culture.
  • An inclusive and ethical workplace.
  • Compensation programs that recognize high performance.
  • A variety of benefits dependent on role and location.

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

What you will do:

  • Lead the design, execution, and interpretation of experiments for process development, optimization, and characterization within a GMP environment.
  • Develop and implement innovative analytical methods to support drug substance and drug product development.
  • Troubleshoot complex technical issues and propose effective solutions in a timely manner.
  • Author and review technical reports, protocols, and regulatory documents.
  • Present research findings to internal and external stakeholders.
  • Mentor and guide junior scientists, fostering their professional development.
  • Collaborate effectively with cross-functional teams, including process development, manufacturing, quality control, and regulatory affairs.
  • Stay abreast of the latest scientific advancements and industry trends in biopharmaceutical development.
  • Ensure compliance with all relevant safety regulations and company policies.
Show full description

What we are looking for:

  • Ph.D. in Biochemistry, Molecular Biology, Chemical Engineering, or a related scientific discipline with 5+ years of relevant industry experience, or M.S. with 8+ years of experience, or B.S. with 10+ years of experience.
  • Solid oral dosage 5-10 years of solid oral dosage development experience, DPI (Drug Products Inhalation) experience preferred.
  • Working knowledge of regulations to our industry preferably ICH/ICHQ8 practices.
  • Extensive hands-on experience in mammalian cell culture, upstream/downstream process development, or analytical method development for biologics.
  • Demonstrated expertise in experimental design (DOE) and statistical data analysis.
  • Strong understanding of cGMP regulations and regulatory requirements for biopharmaceutical products.
  • Excellent written and verbal communication skills, with the ability to present complex scientific data clearly and concisely.
  • Proven ability to lead projects independently and effectively manage multiple priorities.
  • Strong problem-solving skills and a proactive approach to scientific inquiry.
  • Proficiency in relevant software for data analysis and scientific reporting.

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 value diversity and are committed to creating an inclusive environment for all employees. 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.

Staying safe while you apply

  • Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
  • Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
  • Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.

Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.

Preparing for this role with ROLIVA

  • Check the fit.

    Compare the requirements with the experience you have confirmed, including gaps.

  • Prepare honestly.

    Build interview stories and application drafts from your own evidence.

  • Keep track.

    Save the role and record your own application status and follow-ups.

Create a free workspace or log in.

Data scientist jobs in United States

ROLIVA currently lists 378 open roles like this in United States.

Employers hiring for this

  • Capital One Financial49 open roles
  • Guidehouse26 open roles
  • RELX23 open roles
  • Socure12 open roles
  • Visa11 open roles

Top skills asked for

Listings whose description mentions each term. A mention is not a requirement.

Advertised salary for this role here

These are advertised ranges, not what people are paid.

  • USD a year, after annualising126,000–423,000 (39 listings, 14 employers)

At a glance

  • Employment typeFull time
  • Employer posted
  • Added to ROLIVA
  • Last checked

Explore similar roles

Similar jobs