Overview
Remote
Depends on Experience
Accepts corp to corp applications
Contract - W2
Contract - Independent
Contract - 6 Month(s)
No Travel Required
Skills
MES
MES OpCenter
Manufacturing Systems
Supply Chain
Siemens Opcenter
Camstar
GxP
Job Details
Position: Lead Engineer MES Opcenter
Remote
Duration: 6 months with opportunity for extension or conversion
Job Description:
Lead Engineer MES OpCenter
The Lead Engineer will lead a team of technical resources to design, develop, configure, and test MES (Manufacturing Execution Systems) solutions. They will be directly responsible for leading resources contracted via a third-party and through other client organizations to develop & deploy MES application software to Medical Device manufacturing sites globally.
The Lead Engineer will lead a team of technical resources to design, develop, configure, and test MES (Manufacturing Execution Systems) solutions. They will be directly responsible for leading resources contracted via a third-party and through other client organizations to develop & deploy MES application software to Medical Device manufacturing sites globally.
The Lead Engineer will be responsible for:
- Act as subject matter expert on system design and architecture.
- Solving and designing new functionality.
- Provide innovative ways of problem-solving and implementing system improvements.
- Look for out-of-the-box solutions to new requirements or to deprecate prior customizations.
- Be the single point of contact for the technical deliverables of the project and know the status, risks, and issues at all times, and coordinate/provide reports outs & updates to leadership teams and stakeholders.
- Application development oversight, ensuring quality and timely delivery of project execution and completion.
- Hands-on application development on occasion to resolve issues and lead by example.
- Work with other stakeholders and team members to identify, manage, and resolve risks.
- Escalate and track cross-squad dependencies and impediments before they affect project deliverables, timeline, or cost.
- Lead a team of internal and external professionals, geographically dispersed.
- Mentor, coach, and teach other technical team members on best practices/principles.
- Ensure IT compliance (WICO, HIPAA, GXP, 21 CFR Part 11, Records Management, SOX, SDLC, CSV) requirements in all activities and solutions are delivered.
Qualifications:
- 5 years' experience supporting Supply Chain/Manufacturing Systems required.
- Experience in regulated manufacturing required (medical device preferred).
- Experience in a Siemens Opcenter/Camstar technical role (hands-on) required.
- Experience in application development and support is required.
- Experience in project management and delivery with benefits delivered as committed and required.
- Experience in GxP systems, Computer System Validation, and a consistent track record in the support of FDA-regulated systems and business is required.
- Strong interpersonal skills required. Excellent communication, networking, and influencing skills, including the ability to manage across all management and organizational levels required.
- The ability to manage and drive multiple projects simultaneously is required.
- Experience with application interface design and development (Rest API, for example) preferred.
- Ability to work autonomously as an empowered leader.
- Vendor management experience preferred.
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