Software Engineer – Tulip; Manufacturing Medical Device Industry and Tulip

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

Position : Software Engineer – Tulip (Experience in Manufacturing Medical Device Industry and Tulip)

Location : Milpitas, CA

Duration : 3 Months

Total Hours/week : 40.00

Shift : 1st Shift

Client : Medical Devices Company

Job Category : IT

Level of Experience : Senior Level

Employment Type : 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 monitoring 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 adherence 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.