Research Scientist III

Lonza Group Ltd.; Tampa (FL); On-site; USD 110,000 - 140,000; Full time

Job summary

Lonza Group Ltd. in Tampa, FL seeks a Research Scientist III to lead design, execution, and interpretation of experiments for process development in a GMP environment.

You will develop analytical methods to support drug substance and product development and mentor junior scientists while partnering with cross‑functional teams. Responsibilities include data interpretation, report writing, and presenting findings to stakeholders, with a focus on innovation and regulatory compliance in

Qualifications

• Ph.D. required with 5+ years of industry experience or MS with 8+ years or BS with 10+ years.
• Solid oral dosage development experience (5–10 years)
• DPI experience preferred
• Working knowledge of industry regulations (ICH/ICHQ8)
• Experience in mammalian cell culture and upstream/downstream development or analytical methods for biologics
• Experience in experimental design (DOE) and statistics
• Strong understanding of cGMP and regulatory requirements
• Excellent written and verbal communication skills
• Ability to lead projects and manage multiple priorities
• Proficiency with data analysis and reporting software

Responsibilities

• Lead design, execution and interpretation of experiments for process development, optimization and characterization in GMP.
• Develop and implement analytical methods to support drug substance and product development.
• Troubleshoot complex technical issues and propose effective solutions.
• Author and review technical reports, protocols and regulatory documents.
• Present findings to internal and external stakeholders.
• Mentor and guide junior scientists; foster their development.
• Collaborate with cross‑functional teams in PD, manufacturing, QC and regulatory affairs.
• Stay current with scientific advancements and industry trends.

Skills

Mammalian cell culture

Upstream/downstream

Analytical method development

DOE

Statistics

cGMP

Regulatory knowledge

Data analysis software

Scientific reporting

Written & verbal communication

Education

Ph.D. in Biochemistry, Molecular Biology, Chemical Engineering, or related discipline

M.S. in Biochemistry, Molecular Biology, Chemical Engineering, or related discipline

B.S. in Biochemistry, Molecular Biology, Chemical Engineering, or related discipline

Tools

DOE software

Regulatory frameworks (ICH)

Job description

Research Scientist III Tampa, FL The actual location of this job is in Tampa, Florida, US.

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.

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?