Missouri Staffing
Software Engineer - DevOps
It is not every day that you can say the software you helped develop will save hundreds or thousands of lives per year, but at bioMrieux, we put innovation to work in life-saving diagnostic devices deployed across the world. With engineering centers in the United States, France, and Italy, our Systems Development team collaborates globally to build products that ensure patient health and consumer safety. From antibiotic susceptibility testing to organism identification with mass spectrometry, bioMrieux offers challenging opportunities in a science-based domain with a public health focus. If you're passionate about providing real-world solutions, you'll find a home in our team of expert software developers, engineers, and microbiologists. We develop equipment, tests, and software that deliver rapid, high-impact, actionable results in microbiology. The DevOps Software Engineer will be part of the Platform Integration team that supports our software product development teams and lead enhancements to our CI-CD and release management practices. Job Duties: Collaborate with the software product development and testing teams to make further improvements to the Software Development Life Cycle and promote Continuous Integration/Deployment. Create frameworks, services, and applications that support our software product deployment goals. Sustain and improve the process of knowledge sharing within the software engineering team. Improve efficiency by automating repetitive tasks. Evolve the technology and tools utilized to keep the infrastructure up to date. Implement infrastructure-as-code. Create, deploy, and maintain CI/CD pipelines. Manage our CI-CD infrastructure in various environments (development, validation and release/production) and perform effective monitoring. Minimum Qualifications: BS degree required. Computer Science/Software Engineering preferred. 2+ years of development experience with at least 1 year of experience directly in CI-CD and DevOps. 2+ years with: Version control system (Git / GitLab) Windows/Linux administration and scripting experience (PowerShell and Command Batch scripts, Groovy scripting language) Implementing CI/CD pipelines (Jenkins, GitLab CI) Build and continuous integration systems (Gradle, Maven) Configuration management tools (Ansible, Python) Virtualization Management tools (VMware, Hyper-V) Leveraging package managers (Chocolatey and Nuget); experience building custom Chocolatey packages would be a plus. MS Windows images management (ISO, VM templates, etc.) 2+ years experience in authoring technical documentation. 2+ years experience with software development methodologies, especially Agile, Scrum, etc. Review of other team members' application code and test code for correctness and potential improvements. Ability to develop and document deliverables compliant with established company practices. Effective in a fast-paced environment utilizing critical thinking and problem-solving skills with minimal supervision. Strong attention to detail. Proficiency in verbal and written English. Preferred Qualifications: ISO/FDA-regulated environment as a member of a product development organization (medical device or biotech industry) delivering under design control and regulatory statutes. 1+ years Experience cooperating with multi-located teams.
It is not every day that you can say the software you helped develop will save hundreds or thousands of lives per year, but at bioMrieux, we put innovation to work in life-saving diagnostic devices deployed across the world. With engineering centers in the United States, France, and Italy, our Systems Development team collaborates globally to build products that ensure patient health and consumer safety. From antibiotic susceptibility testing to organism identification with mass spectrometry, bioMrieux offers challenging opportunities in a science-based domain with a public health focus. If you're passionate about providing real-world solutions, you'll find a home in our team of expert software developers, engineers, and microbiologists. We develop equipment, tests, and software that deliver rapid, high-impact, actionable results in microbiology. The DevOps Software Engineer will be part of the Platform Integration team that supports our software product development teams and lead enhancements to our CI-CD and release management practices. Job Duties: Collaborate with the software product development and testing teams to make further improvements to the Software Development Life Cycle and promote Continuous Integration/Deployment. Create frameworks, services, and applications that support our software product deployment goals. Sustain and improve the process of knowledge sharing within the software engineering team. Improve efficiency by automating repetitive tasks. Evolve the technology and tools utilized to keep the infrastructure up to date. Implement infrastructure-as-code. Create, deploy, and maintain CI/CD pipelines. Manage our CI-CD infrastructure in various environments (development, validation and release/production) and perform effective monitoring. Minimum Qualifications: BS degree required. Computer Science/Software Engineering preferred. 2+ years of development experience with at least 1 year of experience directly in CI-CD and DevOps. 2+ years with: Version control system (Git / GitLab) Windows/Linux administration and scripting experience (PowerShell and Command Batch scripts, Groovy scripting language) Implementing CI/CD pipelines (Jenkins, GitLab CI) Build and continuous integration systems (Gradle, Maven) Configuration management tools (Ansible, Python) Virtualization Management tools (VMware, Hyper-V) Leveraging package managers (Chocolatey and Nuget); experience building custom Chocolatey packages would be a plus. MS Windows images management (ISO, VM templates, etc.) 2+ years experience in authoring technical documentation. 2+ years experience with software development methodologies, especially Agile, Scrum, etc. Review of other team members' application code and test code for correctness and potential improvements. Ability to develop and document deliverables compliant with established company practices. Effective in a fast-paced environment utilizing critical thinking and problem-solving skills with minimal supervision. Strong attention to detail. Proficiency in verbal and written English. Preferred Qualifications: ISO/FDA-regulated environment as a member of a product development organization (medical device or biotech industry) delivering under design control and regulatory statutes. 1+ years Experience cooperating with multi-located teams.