Expires soon Medtronic

Adv. Mfg. Engineering Extrusion Intern

  • Internship
  • Danvers (Essex County)
  • Design / Civil engineering / Industrial engineering

Job description

Provide engineering support in the concept, prototyping, clinical evaluation, process/equipment development and production scale up of new products and components from R&D, Supply Chain, manufacturing transfers and business acquisitions. Provide engineering support in product transfers from R&D to Manufacturing. Provide engineering support in product line transfers from outside facilities to internal manufacturing in Massachusetts. Provide engineering support in product line transfers from current manufacturing to outsourced manufacturing vendors. Provide engineering support scale up of component manufacturing for other businesses within Medtronic. Define equipment, process, material and operator specifications for manufacturing. Approach all engineering activities with the objective to reduce variability in operator, materials, machines and manufacturing processes to improve profitability at the Danvers site.
_______________________________________________________________
Responsibilities
Contribute to the solution of product and process problems using experimental methods, statistical analysis and effective writing and presentation skills.
• Dexterity, fine motor skills, ability to fabricate catheter based medical devices
• Conduct experimentation and analysis of data and present for peer review and approval.
• Develop and participate in the validation of new manufacturing processes.
• Interface with vendors and personnel at other Medtronic facilities.
• Carry out Process and Tooling Development efforts with an end goal of successfully completing Process Ranging, Characterization and Validation in support of achieving commercialization objectives and timelines.
• Provide input to the tooling engineers and machine shop in the design, building and implementation of new tooling in support of manufacturing ramp up and transfer.
• Develop manufacturing specs in support of new product introduction.
• Participate in cross-functional or departmental team projects as required.
• Insure compliance to Corporate, Divisional and Site Process Validation procedures and policies.
• Prioritize and balance workload of multiple project assignments based on business and functional objectives.
• Perform other related tasks as required.

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
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
Microscope use is required.
ABOUT MEDTRONIC:
Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology 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 can accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future.

EEO STATEMENT:
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.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here: http://www.uscis.gov/e-verify/employees
DISCLAIMER:
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.

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Desired profile

Basic Qualifications:
Enrolled in a BS/MS degree program in an Engineering discipline – preferably Plastics, Mechanical, Materials or Biomedical
Desired/Preferred Qualifications:
• Medical device engineering experience
• Technical writing skills
• Mechanical drafting skills
• Knowledge of medical device development concepts
• Working knowledge of MS Office
• Knowledge of GMPs and ISO9000 rquirements
• Knowledge of manufacturing processes and quality standards
• Statistics
• Previous work experience, preferably in a manufacturing setting
• Exhibit sound judgment in the formulation and solution of problems
• Effective verbal and written communication, analytical and interpersonal skills
• Able to communicate at all levels and across company lines
• PC skills

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