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Manufacturing System Engineer
Job in
Milpitas, Santa Clara County, California, 95035, USA
Listed on 2026-01-11
Listing for:
Planet Pharma
Full Time
position Listed on 2026-01-11
Job specializations:
-
Software Development
Software Engineer
Job Description & How to Apply Below
Senior National Recruiter and R&D IT Lead
The candidate will be responsible for creating and documenting applications within a cloud-based manufacturing execution system called Tulip. The 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.
$40.00/hr - $60.00/hr
Responsibilities- Work independently to specify, plan, design, develop, test and support software components
- 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 development policies and procedures
- Ensure compliance with regulatory requirements including 21 CFR part 11 requirements, 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
- Minimum 3 years of relevant experience is required
- 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
- Excellent written and oral communication and interpersonal skills are essential
- Experience in MES development
- Experience working in an FDA/ISO-regulated environment
- Experience with Power BI
- Software development with a focus on UX design
- IT infrastructure/ hardware knowledge
- Mid‑Senior level
- Contract
- Information Technology and Manufacturing
- Medical Equipment Manufacturing and Software Development
- Medical insurance
- Vision insurance
- 401(k)
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