Sr. Web Developer

Senior Web Developer

Location: Morristown, New Jersey

As the sole technical owner of Capsugel.com, you will shape, secure, and evolve a high‑visibility website in a regulated enterprise environment. This is a unique opportunity to lead end‑to‑end development and governance for a mission‑critical digital platform that supports a global pharmaceutical audience.

What you will get:

• An agile career and dynamic working culture.

• An inclusive and ethical workplace.

• Compensation programs that recognize high performance.

• The full list of our global benefits can be found here:

What you will do:

• Serve as the single technical owner of Capsugel.com, ensuring stability, availability, and controlled change management.

• Lead the full lifecycle of website development, architecture, deployment, and long‑term maintainability.

• Design, build, and maintain responsive, accessible web pages using modern front‑end technologies (HTML5, CSS3, JavaScript).

• Own and strengthen the site’s security posture, including secure coding, data privacy, encryption, and access controls.

• Ensure ongoing compliance with SEO, accessibility (WCAG), performance, and regulatory/quality requirements.

• Proactively identify risks, implement preventative controls, and maintain audit‑ready documentation.

• Collaborate with marketing, legal, regulatory, quality, and IT security to deliver compliant, user‑centered digital solutions.

What we are looking for:

• Bachelor’s degree in science, Information Technology, Computer Systems, or Computer Engineering required.

• 8+ years of professional web development experience with proven ownership of enterprise websites required.

• Strong expertise in HTML5, CSS3, JavaScript (ES6+), website security, SEO, and performance optimization.

• Experience working in regulated or compliance-driven environments (pharma, biotech, life sciences preferred).

• Ability to independently manage development, documentation, and controlled change processes.

• Knowledge of WCAG accessibility standards and privacy regulations (e.g., GDPR).

• Familiarity with GxP concepts, validation principles, and audit support is a plus.

• Experience with enterprise CMS or headless CMS platforms and cross-functional stakeholder collaboration.

• Must reside within a commutable distance of one of our CHI locations: Tampa, FL; Greenwood, SC; Morristown, NJ; Cohasset, MA; or Colmar, FR.

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 offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. 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.