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Looking Onsite || Senior Development Engineer Manufacturing Medical Device || Irvine, CA (Onsite) at Irvine, Kentucky, USA
Email: [email protected]
From:

Rhitik Gaur,

Quantum World It

[email protected]

Reply to:   [email protected]

Good evening,

I hope all is well with you

For the following, Quantum World IT is seeking the best consultant profile.

Please respond with your most recent resume if you are considering new opportunities.

Looking Onsite ||

Senior Development Engineer Manufacturing Medical Device || Irvine, CA (Onsite)

Must Have Technical/Functional Skills

Knowledge of good manufacturing practices and documentation, preferably in the medical industry.

Ability to read, interpret, redline and make recommendations on engineering drawings.

Tolerance stackup, GD&T experience, preferably

Six Sigma Green belt certification, preferably

PMI Project Management Professional certification, preferably

Knowledge of various manufacturing processes to make metal, plastic and/or electrical components.

Knowledge of computer programs.

Oral and written communication in English.

Comprehension of standard costs and work standards.

Experience Required

A minimum of 5 years of experience in work-related engineering experience

Prior experience in New Product Development working in a team environment.

Previous experience in the areas of Design for Manufacturing or Assembly

Excellent communication and collaboration capabilities

Experience working closely with external suppliers (Required)

Performance within a medical device production environment or other regulated environment (Preferred)

Measurement Systems Analysis (i.e. GR&R)

Statistical Analysis knowledge (i.e. Design of Experiments, Process Stability/Control/Capability)

Roles & Responsibilities

Under (e.g. limited supervision, general direction, etc.) and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

Lead the design, development, qualification, and stabilization of component (metal, plastic, electrical or other) and process solutions.

Own process development, qualification, and control for component and assembly solutions

Serve as an integral part of NPD teams on Design for Manufacturing/Assembly/ Cost and drive robust product and process development that meets business commitments and stabilization metrics.

Design and develop robust equipment, tooling, and manufacturing processes to meet product requirements in compliance with User requirements, Quality, Regulatory, Safety and Ergonomic standards.

Incorporate risk mitigation methodology to drive process stability and capability.

Identify and implement standard methodologies of project management through component development.

Responsible for developing new manufacturing and assembly processes consistent with Design for Manufacturability for new product introductions.

Responsible for communicating business related issues or opportunities to next management level.

Responsible for ensuring personnel and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.

Performs other duties assigned as needed.

Generic Managerial Skills

Strong communication skills. Candidates must be highly proficient in reading, writing, and speaking English language.

Work within a multi-discipline team.

Education

A minimum of a Bachelors degree, preferably in Engineering

Keywords: rlang information technology California
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Fri Mar 22 06:39:00 UTC 2024

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