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Software Developer; Greenwood, SC - Hybrid

Job in Greenwood, Greenwood County, South Carolina, 29648, USA
Listing for: Lonza Biologics Porriño SLU
Full Time position
Listed on 2025-12-01
Job specializations:
  • Software Development
    Software Engineer, C# / Unity Developer
Job Description & How to Apply Below
Position: Software Developer (Greenwood, SC - Hybrid)

Software Developer (Greenwood, SC - Hybrid)

United States, Greenwood (South Carolina)

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world.

And that’s the kind of work we want to be part of.

This is a full-time, hybrid role based in Greenwood SC. Greenwood SC is home to a collaborative and innovative manufacturing environment, offering opportunities to work with cutting‑edge technologies in life sciences. As a Software Developer, you will play a pivotal role in designing, developing, and maintaining software applications and systems that power our production environment. You will work closely with cross‑functional teams to deliver solutions that optimize capsule production workflows, inventory management, and data integrity.

What

you will get
  • An agile career and dynamic working culture
  • An inclusive and ethical workplace
  • Compensation programs that recognize high performance
  • Medical, dental and vision insurance
  • The full list of our global benefits can also be found on
What you will do
  • Design, develop, and maintain robust software applications using .NET Framework/Core, C#, and SQL Server to support production systems
  • Collaborate with stakeholders to gather requirements and implement scalable solutions integrated with ERP and MES systems
  • Perform code reviews, debugging, and optimization to ensure high performance and uptime in a 24/7 production environment
  • Implement and maintain database schemas and queries in SQL Server ensuring compliance with 21 CFR Part 11
  • Support system validation, testing, and deployment activities including UAT aligned with pharmaceutical regulations
  • Troubleshoot and resolve production issues promptly, minimizing downtime and maintaining system integrity
  • Document software designs, processes, and changes to facilitate knowledge transfer and regulatory audits
What we are looking for
  • Bachelor’s degree in computer science, Information Technology, or a related field (or equivalent experience) required.
  • Proficiency in object-oriented programming, ASP.NET (MVC/Web API), Entity Framework, and
  • Strong SQL skills including query optimization, indexing, and ETL processes
  • Experience with version control systems (e.g., Git) and agile development methodologies (e.g., Scrum)
  • Familiarity with pharmaceutical or regulated industries including GxP and validation lifecycle
  • Excellent problem-solving skills and ability to work under pressure in a production setting
  • Strong communication skills to explain technical concepts to non-technical stakeholders
  • Travel
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