Senior Associate Software Engineer

Sr. Associate Software Engineer

As a Senior Associate Software Engineer at Amgen, you will be responsible for developing and maintaining software applications to meet business needs. You will collaborate with a team of software engineers, participate in the full software development life cycle, and ensure the delivery of high-quality code and solutions. Your strong programming skills, problem-solving abilities, and attention to detail will contribute to the development of robust and scalable software solutions.

Responsibilities

• Design, develop, and maintain secure, scalable applications and integrations across QC and commercial platforms (AWS, Databricks, Salesforce Marketing Cloud, Mulesoft, LIMS, ELN, and CDS).
• Serve as a system owner by managing lifecycle activities (configuration, validation, upgrades, change control, documentation, and audit readiness) in compliance with GxP and 21 CFR Part 11 requirements.
• Collaborate with business analysts, developers, and stakeholders to gather requirements, deliver validated solutions, and support Agile/DevOps practices.
• Champion continuous improvement by troubleshooting issues, optimizing workflows, and evaluating new platform capabilities to enhance business value and user experience.

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a person with these qualifications.

Would you like to take your software engineering skills and help deliver the world's most advanced and life-changing biotech medicines? If you are excited to work on latest and greatest technology stack, we are looking for you. The Associate will work with some of the brightest minds in the industry and get opportunities to solve some of the most challenging business problems. At Amgen, your work will improve the lives of millions of patients around the world.

Responsibilities

• Serve as the System Owner for Quality Control Laboratory Platforms (Sample Manager LIMS, Biovia OneLab ELN) ensuring the platform is compliant, validated, secure, and aligned with regulatory requirements (e.g., GxP, 21 CFR Part 11, data integrity standards).
• Own the system lifecycle — oversee implementation, upgrades, validation, and retirement activities, following Amgen's system development life cycle (SDLC) and change management processes.
• Act as the primary liaison between product team, support team and client facing technology leads.
• Collaborate closely with developers and technical teams to design, configure, integrate, and validate enhancements, extensions, and interfaces (e.g., to LIMS, data lakes, or other lab systems).
• Lead and coordinate validation activities, including authoring/reviewing test scripts, managing traceability matrices, and supporting audit readiness.
• Manage integrations and data workflows between OneLab ELN and supporting systems, ensuring seamless interoperability and secure data exchange.
• Maintain system documentation including requirements, design, SOPs, training materials, validation documents, and user guides.
• Monitor vendor product roadmaps for Biovia OneLab ELN and evaluate applicability to Amgen's business needs; drive adoption of new features when beneficial.
• Ensure audit readiness by maintaining compliant system records, addressing deviations/incidents, and supporting regulatory inspections.
• Champion best practices and innovation in digital lab solutions, helping to modernize workflows while maintaining compliance and quality standards.
• Contribute to Agile ceremonies (standups, sprint planning, retrospectives) and support DevOps/CI/CD activities as applicable.

Basic Qualifications

Master's degree

OR

Bachelor's degree and 2 - 6 years of Information Science experience

Preferred Qualifications

• 2 years of direct experience with Biovia OneLab ELN, THermo Fisher Sample Manager LIMS or comparable ELN solutions (e.g., Biovia Workbook, LabWare, Labguru).
• Strong understanding of system ownership responsibilities including:

GxP compliance, 21 CFR Part 11 requirements, and validation

System lifecycle management, change control, and audit readiness

Ensuring data integrity and security of scientific records

• Proven experience integrating and validating systems within a regulated environment (GxP, FDA, EMA).
• Experience with integrating OneLab ELN, LIMS into broader Operations, R&D and IT ecosystems (e.g., LIMS, inventory systems, data warehouses).
• Familiarity with scientific workflows (biologics, chemistry, lab processes) and ability to translate them into digital solutions.
• Hands-on technical skills with SQL, Python, AWS, and APIs for data workflows, automation, and system integration.
• Knowledge of DevOps/Agile practices, release management, and vendor management for SaaS/enterprise platforms.
• Strong communication skills with the ability to define, document, and understand customer requirements, ensuring alignment between business needs and technical delivery.

Thrive

Some of the vast rewards of working here

As we work to develop treatments that take care of others, we also work to care for our teammates' professional and personal growth and well-being.

• Full support and career-development resources to expand your skills, enhance your expertise, and maximize your potential along your career journey
• A diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
• Generous Total Rewards Plan—comprising health, finance and wealth, work/life balance, and career benefits—with compensation and benefits rated above 4 stars (out of 5) on Glassdoor

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.