Healthcare ofertas em United States

As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.

Teleflex is the home of Arrow, Barrigel, Deknatel, QuikClot, LMA, Pilling, Rüsch, UroLift and Weck – trusted brands united by a common sense of purpose.

At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.

Global Operations is a complex and diverse organization within the company which is responsible for product fulfilment to all our customers from end to end. We pride ourselves on being totally Customer Centric in our unrelenting focus on Improving Quality, Service and Value as perceived by our customers. Our employees are dedicated to the Global Operations Enterprise Excellence journey. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients’ lives.

1. Engineering lead for Sustaining, NPI and research, activities to implement new or redesigned products, processes, components, and formulations. Identify and create new design and/or process concepts.
2. Function as primary engineering resource on materials, special projects and project improvements as required.
3. Serve as project leader or guide the development engineers for the project plan with critical milestones & timeline and with the responsibility to follow up on all aspects of projects including reviews with the support groups and outside resources where applicable.
4. Interface with clinicians, marketing, and process development to understand customer preferences/requirements and establish necessary design criteria for new products and product improvements.
5. Develop and coordinate the running of protocol for the validation of new, modified devices or components including validations of design, manufacturing, assembly, packaging, and sterilization & where applicable support group departments such as engineering, regulatory, documentation, tooling & manufacturing.
6. Lead, conduct and/or participate in design and technical phase reviews.
7. Interface with purchasing, vendors, and marketing to develop new components/products/technologies by providing technical requirements and assisting with supply agreements.
8. Update and review project progress on an as required basis by manager.
9. Interface with process development engineers, manufacturing, and lab technicians to design and develop new fixtures, tooling, and machinery. Assist in the development and qualifications of required manufacturing processes.
10. Develop new products and product concepts using existing and emerging technologies per Design Control requirements and Concept to Commercial (C2C).
11. Contribute to our culture that thrives on core values, with people at the center of all we do. Working together, our shared values of Entrepreneurial Spirit, Building Trust, and Make It Fun allow us to produce outstanding products and services that genuinely make a difference to people's lives around the world.
12. Serve as a mentor for engineering personnel on clinician interaction, product design development, verification/validation testing, documentation, and manufacturing related processes.
13. Represent the engineering department at hospitals, scientific sessions, and seminars to meet medical personnel and discuss product line requirements and trends.
14. Document all new ideas for products and/or processes as Company's intellectual property. Work with Patent Attorney’s to file new patents and assess infringement potentials.
15. Assist process development and manufacturing personnel with the transfer of development projects and design changes into production.
16. Support regulatory submissions and clinical trials as required.
17. And any other assignment/task as deemed fit.

Qualification:
Must have an undergraduate degree in a related engineering/material science field, graduate or advanced degrees strongly preferred.

Experience:
a) Typically requires a minimum of 7 years of related experience with a Bachelor’s degree in Mechanical Engineering, Polymer Engineering or other related engineering fields.
b) Preferably with minimum 7 years working experience in medical devices and R&D environment.
c) Strong Preference for min 7 years in Medical Device.
d) Knowledge and experience with Tracheostomy a strong advantage.
e) Strong analytical and problem-solving skills.
f) Effective verbal and written communication skills.
g) Team player with good interpersonal skills.
h) Proficient in Microsoft Office Suite and computerized analysis applications.
i) Proficient in tool design, stack up of tolerances, Solid work.
j) Self-motivated, high energy, positive attitude with initiative and drive for timely completion of goals.
k) Able to travel domestically and internationally.
l) Familiarity with ISO 13485, MDR, FDA 21 CFR Part 820 Design Control, ISO 14971, GMP and other standards as they relate to the development and manufacture of medical device would be an advantage.

Note: As with all positions, due to the dynamic nature of Teleflex Medical business, key responsibilities may evolve and change over time.

Teleflex is an equal opportunities employer.

At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.