Lead Engineer – Lead Engineer | Priority – Interview immediately (please provide genuine candidate only)

Position:  Lead Engineer – MES Opcenter 
 Location: Remote
Duration: 6 months with opportunity for extension or conversion
Company:  Johnson & Johnson  – Cognizant

Pay: $70/hr on C2C

45665-1: Opcenter, interviews: candidates unable to answer what’s in their resume, will be having a spotlight call.

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 J&J 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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Thanks and regards,
Badaline Paliar
US IT Recruiter | TechDigital Corporation & Omni Inclusive LLC