Summary

Lonza is a pioneering global Contract Development and Manufacturing Organization (CDMO) and a world leader in pharmaceutical manufacturing services. Founded in 1897 in Switzerland, the company has evolved into the first and original CDMO, now operating as one of the largest Western CDMO networks with approximately 19,000 employees across more than 30 sites spanning five continents. Lonza specializes in transforming therapeutic discoveries into life-saving and life-enhancing treatments for patients worldwide. The company's comprehensive services span from early development to drug substance and drug product manufacturing, covering established and emerging technologies including mammalian biologics, small molecules, highly potent APIs, bioconjugates, mRNA, microbial products, and cell and gene therapies. With a focus on cutting-edge science, smart technology, and lean manufacturing, Lonza serves a diverse customer base ranging from emerging biotechs to global pharmaceutical companies, delivering integrated solutions throughout the entire treatment lifecycle.

Job description

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.
Experience with advanced analytical techniques relevant to biopharmaceutical characterization (e.g., HPLC, Mass Spectrometry, CE, SPR).
Strong problem-solving skills and a proactive approach to scientific inquiry.
Proficiency in relevant software for data analysis and scientific reporting.

Requirements

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.
Experience with advanced analytical techniques relevant to biopharmaceutical characterization (e.g., HPLC, Mass Spectrometry, CE, SPR).
Strong problem-solving skills and a proactive approach to scientific inquiry.
Proficiency in relevant software for data analysis and scientific reporting.

Benefits

Relocation assistance
Compensation programs
Global benefits

Company overview

Lonza is a pioneering global Contract Development and Manufacturing Organization (CDMO) and a world leader in pharmaceutical manufacturing services. Founded in 1897 in Switzerland, the company has evolved into the first and original CDMO, now operating as one of the largest Western CDMO networks with approximately 19,000 employees across more than 30 sites spanning five continents. Lonza specializes in transforming therapeutic discoveries into life-saving and life-enhancing treatments for patients worldwide. The company's comprehensive services span from early development to drug substance and drug product manufacturing, covering established and emerging technologies including mammalian biologics, small molecules, highly potent APIs, bioconjugates, mRNA, microbial products, and cell and gene therapies. With a focus on cutting-edge science, smart technology, and lean manufacturing, Lonza serves a diverse customer base ranging from emerging biotechs to global pharmaceutical companies, delivering integrated solutions throughout the entire treatment lifecycle.