Software Engineer - Tulip; Manufacturing Medical Device Industry and Tulip

Position

Software Engineer - Tulip (Experience in Manufacturing Medical Device Industry and Tulip)

Milpitas, CA

3 Months

40.00

1st Shift

Medical Devices Company

IT

Senior Level

Contract on W2 (Need US Citizens or GC Holders or GC EAD or OPT or EAD or CPT)

• The candidate will be responsible for creating and documenting applications within a cloud-based manufacturing execution system called Tulip.
• This candidate will collaborate design efforts with multiple teams to ensure that paper-based manufacturing and quality processes are accurately translated to electronic form.
• The candidate must be self-directed requiring minimal daily direction while collaborating with the team to achieve agreed upon scheduled deliverable work.
• The candidate will participate in an Agile software team.

• Work independently to specify, plan, design, develop, test and support software components assigned
• Contribute to project schedule generation including scope of work, duration of tasks, and order of execution
• Monitor work progress against schedule commitments, reports progress to leadership in a timely fashion, including when work will not be completed according to schedule milestones
• Propose solutions to maintain schedule milestones including prioritizing efforts and monitor scope creep
• Work with team to establish necessary requirements specifications and test plans for software product validations
• Responsible for translating requirements into design and implementation of well-structured and documented software components
• Implement new software component designs or enhancements to existing software products; participate in the implementation of more complex subsystems and systems
• Troubleshoot/debug issues within existing automation systems and implement modifications to resolve these issues
• Participate in technical design reviews and code inspections
• Insure adherence to client development policies and procedures
• Ensure compliance with regulatory requirements including 21 CFR part 11 requirements, client quality standards, and conveys an expectation of high-quality software

• Require a BS degree in Computer Science, Process Engineering, Continuous Improvement, or a related Engineering discipline with software development experience
• Excellent written and oral communication and interpersonal skills are essential
• Minimum 3 years of relevant experience
• Knowledge of software development in a process oriented/regulated environment and adhering to a quality management system
• Experience with Agile software development
• Knowledge of Automation/Process Control experience

• Application development experience using Tulip
• Experience in MES development
• Experience working in an FDA/ISO-regulated environment
• Experience with software languages including C#, JavaScript and SQL Server
• Experience with Power BI
• Software development with a focus on UX design
• IT infrastructure/ hardware knowledge