Life-cycle Engineer, Associate

Found in: Talent US C2 - 2 weeks ago

Chester, United States ZEISS Group Full time

About Us:

How many companies can say they’ve been in business for over 177 years?

Here at ZEISS, we certainly can As the pioneers of science, ZEISS handles the everchanging environments in a fast-paced world, meeting it with cutting edge of technologies and continuous advancements. ZEISS believes that innovation and technology are the key to a sustainable future and solutions for global change. We have a diverse range of portfolios throughout the ZEISS family in segments like, Industrial Quality & Research, Medical Technology, Consumer Markets and Semiconductor Manufacturing Technology. We are a global company with over 42,000 employees and have over 4,000 in the US and Canada alone Make a difference, come join the team

What’s the role?

As part of R&D, apply fundamental engineering skills to complete life-cycle development activities for existing products within the ophthalmic and neurosurgical device portfolios

Sound Interesting?

Here’s what you’ll do:

Contribute to the upkeep of the existing devices and manufacturing processes Execute product design changes for existing devices due to, but not limited to, CAPAs, product complaints, COGS reduction efforts, and component obsolescence Work in a cross functional team, collaborating with engineers, QA/RA specialists, marketing personnel, and manufacturing employees for life-cycle projects Contribute to the registration efforts of existing devices for the EU market Create and maintain documentation for product specific DHF (design history files) and DMR (device master records) Maintain technical drawings for product components and assemblies Manage engineering change requests related to product design changes Improve manufacturing processes and fixtures for assembly of existing devices Improve inspection procedures for quality control of existing components and assemblies Create process validation protocols and reports, conducting hands-on testing to gather applicable data Ensure the compliance of the design controls procedure, by working closely with regulatory personnel during design change activities Identify and implement improvements to established products and processes, by working closely with regulatory and manufacturing personnel Preparation and participation in internal and external audits Provide technical input to marketing and regulatory personnel regarding projects within your work cell Oversee technical issues with component suppliers Create project schedules in the form of Gantt charts and action item lists Provide accurate completion date and remaining work estimates for project managers Communicate on the progress of projects Other duties may be assigned

Do you qualify?


QUALIFICATIONS  

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Experience with design and development processes Experience with design change processes Experience with drafting/CAD software, preferably SolidWorks Experience with DHFs and DMRs Proficiency in Microsoft Office applications, including Word and Excel Great attention to detail, especially proofreading of documentation prior to submittal Strong organizational skills Ability to multi-task on different projects, while maintaining high quality performance Strong communication skills, both written and spoken Ability to work cross-functionally with a team, including engineering, regulatory, marketing, and manufacturing personnel Ability to problem solve and think outside of the box The desire to be hands-on and involved through the entire process Proficient at technical problem-solving Proficient in technical writing Knowledge and experience of engineering change-management processes

EDUCATION and/or EXPERIENCE

1 years of industry engineering experience required (relevant internships/co-ops will be considered in place of industry experience) Bachelor’s degree in engineering, preferably in mechanical, manufacturing, or biomedical engineering

We have amazing benefits to support you as an employee at ZEISS

Medical Vision Dental 401k Matching Employee Assistance Programs Vacation and sick pay  The list goes on 

ZEISS is an EEO/AA/M/F/Disabled Veteran Employer

Your ZEISS Recruiting Team:

Clara Cresswell

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