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1+ months

Senior Manufacturing Engineer

Medtronic
Danvers, MA 01923
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Senior Manufacturing Engineer

Location:

Danvers 35 Cherry Hill, Massachusetts, United States

Requisition #:

20000M1Q

Post Date:

Dec 15, 2020


**Careers that Change Lives**

**MAIN PURPOSE OF JOB**


Develops manufacturing methods, systems, equipment and processes on existing products to produce a high quality product at optimal cost.


**MAIN JOB DUTIES/RESPONSIBILITIES**


Meet or exceed Manufacturing goals and objectives.

Develop and implement process and product improvements. Typically projects of complex scope and wide magnitude.

Equipment and Fixturing: Determine specific requirements of manufacturing operation in order to specify equipment, fixturing, and process parameters. May collaborate on design with suppliers to fulfill equipment and fixturing requirements.

Qualification and Validation: Develop plans to evaluate process repeatability and stability through equipment qualification and process validation.

Continuous Improvement and Cost Analysis: Improve manufacturing methods, optimize product performance and reduce manufacturing costs in a systematic fashion. Deploy Lean 6 Sigma methodology to identify and evaluate opportunities for improvement inherent in manufacturing processes and make specific recommendations for adoption.

In partnership with Finance, perform detailed cost analyses of manufacturing changes.

Production Support and Trouble Shooting: Provide engineering support to manufacturing operation. Address related issues arising on the production floor. May form and lead inter-disciplinary teams to resolve high profile production issues and document recommended corrective actions using the quality systems procedures. (NCMR CAPA) Ability to lead Failure Investigations.

Develop and Optimize Work Design, Manufacturing Layout and Product Flow: Using Lean Manufacturing principles, recommend and implement process layouts for efficient manufacturing. Recommend appropriate staffing levels to support manufacturing requirement.

Define and generate all required documentation in support of manufacturing protocols, reports, manufacturing instructions and procedures. These include: Engineering protocols, reports, manufacturing instructions and procedures. Ensure compliance with GMPs and internal protocol. Use appropriate statistical support and Design of Experiments (DOE) when developing recommendations.

Compare internal yield/external complaint failure model with the process FMEA and accurately assess quality impact.

Lead teams in operations related programs including product iterations, cost reduction programs, process changes across product lines and manufacturing layout synergies.

Lead the work, manage and develop the talent of direct reports.


**A Day in the Life**

Responsibilities may include the following and other duties may be assigned.


+ Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling.

+ Designs arrangement of machines within plant facilities to ensure most efficient and productive layout.

+ Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance.

+ Adapts machine or equipment design to factory and production conditions.

+ May incorporate inspection and test requirements into the production plan.

+ Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality.

+ Develops manufacturing processes that are applicable to statistical process control, and may develop those techniques.

+ Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques.

+ Ensures processes and procedures are in compliance with regulations.


**Must Have: Minimum Requirements**


+ Bachelors degree required

+ Minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years relevant experience


**Nice to Have**

SKILLS/COMPETENCIES


Design of Experiments, process validation equipment development (IQ/OQ/PQ)

-Project management experience

Small tooling design and development

Knowledge of polymer materials and related processes

Electro-Mechanical troubleshooting skills

Medtronic Engineer Technical Certification

Verbal, written and presentation skills

Technical writing skills

Microsoft Project

Strong statistical skills using Minitab

Six Sigma, Constraint Management and Lean Manufacturing experience preferred

-Team dynamic skills (communication, accountability, decision-making, feedback, meeting management, managing conflict).


JOB EXPERIENCE PREFERRED

Engineering experience with disposable medical devices

Equipment and process Design and Development

Experience with developing equipment and related processes especially molding equipment and polymer bonding (injection molding)

-2-5 years experience in an ISO13485/GMP environment


Some travel required


**About Medtronic**


Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.


We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Lets work together to address universal healthcare needs and improve patients lives. Help us shape the future.


Physical Job Requirements


The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.

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Posted: 2020-12-24 Expires: 2021-03-26
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Senior Manufacturing Engineer

Medtronic
Danvers, MA 01923

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