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
Zeiss provides Equal Employment Opportunity without unlawful regard to an Applicants race, color, religion, creed, sex, gender, marital status, age, national origin or ancestry, physical or mental disability, medical condition, military or veteran status, citizen status, sexual orientation, pregnancy (includes childbirth, breastfeeding or related medical condition), genetic predisposition, carrier status, gender expression or identity, including transgender identity, or any other class or characteristic protected by federal, state, or local law of the employee (or the people with whom the employee associates, including relatives and friends).
