Manufacturing Engineering Manager - Riyadh, المملكة العربية السعودية - Masimo

Masimo
Masimo
شركة تم التحقق منها
Riyadh, المملكة العربية السعودية

منذ أسبوع

Fatima Al-Mansouri

تم النشر بواسطة:

Fatima Al-Mansouri

مسوّقة للمواهب لبيبي
وصف

Job Summary:


The Manufacturing Engineering Manager is responsible for managing the development, improvement, and validation, of new and existing manufacturing processes, equipment, tooling, and fixtures.

This position leads and/or supports production transfers from Masimo HQ and Operations to Saudi Arabia manufacturing plants, implements and supports/utilizes affective manufacturing methodologies, such as Lean/Six Sigma following international regulatory standards (e.g. 21 CFR, Part 820 and ISO 13485:2003). Manages all engineering projects and resolves engineering problems.

You will leverage your technical experience and skills to guide the team in the evaluation of product reliability performance and driving improvement on challenging technical problems.


Duties & Responsibilities:


  • Effectively leads one or more workgroups with a staff of Electro-Mechanical, Automation, Industrial Engineers and Process Engineers as well as IT & IS support functions.
  • Responsible for driving and executing on process design, development and launch of new products
  • Manage the design/specification/purchase/installation of the Company's assembly equipment and tooling;
  • Coordinate the day to day support to production (Customer claims, problem solving, deviations, NCR, yields, process & equipment issues ) to ensure the process is enabled to achieve the operation goals;
  • Coordinate the formulation and release of all pertinent Manufacturing Assembly Procedures, Acceptance Procedures, Inspection Procedures for all personnel in the operation; May rewrite processes to improve detail, incorporate visual aids, with the intent of improving the overall quality of Masimo products;
  • Coordinate performance of process validations (IQ, OQ, PQ) including generating protocols and reports in accordance with 21 CFR Part 820 FDA guidelines.
  • Review and approve protocol and written reports.
  • Provides guidance and/or approval of workgroup technical approaches, products and processes
  • Establish Statistical Process Controls for Manufacturing Operations;
  • Coordinate development of Process Failure Mode and Effects Analyses (PFMEA);
  • Coordinate development and implement lean manufacturing processes to build new products and improve existing processes;
  • Oversee initial product builds (engineering units, pilot units, process validation units) and coordinate a smooth transfer of new products into production;
  • Develop manufacturing plans, project timelines, requirements, specifications and process flow;
  • Work closely with design engineering to proactively influence designs for better manufacturability;
  • Must be able to travel domestically and internationally ;
  • Perform special projects as requested

Minimum & Preferred Qualifications and Experience:


Minimum Qualifications:


  • Five or more years of related experience, with technical staff management experience and project management experience involving coordination of crossfunctional teams;
  • Experience in leading process and equipment development projects to completion.;
  • Excellent conceptual, analytical, and problemsolving ability;
  • Experience with electromechanical assembly and testing
  • Experience with Design for Manufacturability and Assembly (DFMA);
  • Basic device software knowledge Experience with statistical techniques (e.g., DOE, SPC)


  • Excellent computer skills

  • CAD, word processing, and spreadsheets;
  • Good communication skills, both verbal and written, and the ability to effectively interface within a crossfunctional team environment;
  • Experienced in modern manufacturing principles and techniques;
  • Will be required to travel both domestically and internationally, on a periodic basis;
  • Must be PC literate, have excellent organizational and communication skills;

Preferred Qualifications:


  • Knowledge and experience in 21 CFR, Part 820 and ISO 13485:2003 requirements.
  • Experience with semiconductor component packaging
  • Knowledge and experience in CGMP requirements and preferably MDA and ISO medical device requirements;
  • Experience with electrical/optical products

Education:


  • Bachelor's degree in engineering: Mechanical, Electrical, Manufacturing or Industrial Engineering is required.
  • Physical requirements/Work Environment _
This position primarily works in an office and manufacturing/production environment. It requires frequent sitting, standing and walking. Daily use of a computer and other computing and digital devices is required. May stand for extended periods when facilitating meetings or walking in the facilities.

Some local travel is necessary, so the ability to operate a motor vehicle and maintain a valid Driver's license is required.


The physical demands of the position described herein are essential functions of the job and employees must be able to successfully perform these tasks for extended periods.

Reasonable accommodations may be made for those individuals with real or perceived disabilities to perform the essential func
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