Bachelor's, Master's, or Ph.D. in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field.
Significant experience in analytical method development and validation within regulated industries.
Demonstrated leadership in managing technical teams and complex scientific projects.
Minimum of 5 years in cGMP, cGLP, and regulatory compliance.
Hands-on experience with analytical techniques like HPLC, GC, and mass spectrometry.
Proven ability to conduct investigations and apply statistical tools for problem-solving.
Excellent communication and collaboration skills, with a focus on stakeholder engagement.
Responsibilities
Lead scientists and technicians in product and method development.
Drive color development and reformulation projects for hard capsules.
Develop and validate analytical methods for new products and process improvements.
Serve as the technical lead for global stability programs and shelf life studies.
Collaborate with Quality, Regulatory, and R&D teams to address technical challenges.
Conduct complex investigations and root cause analyses using scientific methodologies.
Mentor team members and promote a culture of scientific excellence.
Benefits
Agile career opportunities with impactful scientific programs.
Cross-functional collaboration with various technical teams.
Inclusive workplace that encourages innovation and improvement.
Comprehensive medical, dental, and vision insurance.
Professional development and mentorship opportunities.
Full Job Description
Sr. Scientist, Methods Development (Lonza - Capsugel)
Location: Greenwood, SC
Join Lonza| Capsugel's Greenwood site as a key scientific leader supporting product development, method development, and global stability programs for our Hard Empty Capsule and Dosage Form Solutions businesses. In this highly visible role, you will lead technical teams, drive innovation, and help deliver high-quality solutions that support customers and ultimately improve lives around the world.
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 with opportunities to lead impactful scientific programs and global initiatives.
Exposure to cross-functional collaboration with R&D, Quality, Regulatory, Manufacturing, and global technical teams.
An inclusive and ethical workplace where innovation and continuous improvement are encouraged.
Competitive compensation and benefits programs that recognize high performance.
Medical, dental, and vision insurance, plus retirement and wellness programs.
Professional development opportunities and the ability to mentor and grow technical talent.
The opportunity to influence products and technologies that support the life sciences and pharmaceutical industries worldwide.
What you will do:
Lead scientists, analysts, and technicians supporting product development, method development, and global stability programs.
Drive color development and reformulation projects for hard capsule products to meet customer and regulatory requirements.
Develop, validate, and implement analytical methods that support new product introductions, process improvements, and material characterization.
Serve as the technical lead for global stability programs, generating scientific data used to establish product shelf life and support customer studies.
Partner closely with Quality, Regulatory Affairs, Manufacturing, Safety, and R&D teams to solve technical challenges and support business growth.
Lead complex investigations, root cause analyses, and forensic evaluations of product and process issues using scientific and Six Sigma methodologies.
Mentor and develop team members while fostering a culture of scientific excellence, compliance, and continuous improvement.
What we are looking for:
Bachelor's, Master's, or Ph.D. in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related scientific discipline required.
Significant experience in analytical method development, method validation, product development, or quality control within pharmaceutical, nutraceutical, life sciences, or related regulated industries.
A minimum of 5 years in cGMP, cGLP, CFR requirements, laboratory compliance, and regulatory expectations.
Hands-on experience with analytical techniques such as HPLC, GC, mass spectrometry, HPTLC, PDA, wet chemistry, and other advanced laboratory instrumentation.
Proven ability to conduct investigations, perform data analysis, apply statistical tools, and drive technical problem solving in a manufacturing or R&D environment.
Excellent communication, collaboration, project management, and stakeholder engagement skills, with the ability to influence across multiple functions and global teams.
Prior experience with dietary supplements a huge plus!
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.
