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Create, then complete project test plans, analyze data, perform teardown, and assess results to deliver clear findings
Provide detailed reports in written or verbal format for engineering, biological, and non-technical audiences
Develop test methodology as needed to provide reliability capability
Interact in development of engineering design, analysis and other technical requirements
Understand mechanical and system concept design, perform sensitivity analysis, numeric analysis, fluid analysis, timing analysis, or other design analysis.
Lead test and root-cause analysis for mechanical or electrical subassemblies
Strong communication skills.
Education and Experience:
Required: BS in Engineering (preferred: Electrical, Mechanical, or Biomechanical) with 5+ years test engineering experience
Preferred: MS (Electrical, Mechanical, or Biomechanical) with 3+ years test engineering.
Experience working in a manufacturing/ medical device environment preferred. Knowledge of medical device manufacturing and regulatory compliance a plus.
Solid technical writing experience. Must be able to present information and thought process flow clearly and succinctly with strong presentation skills.
Working knowledge of statistical methodologies, quality control and manufacturing tools, such as applied statistics, lean manufacturing, Six Sigma, etc
Experience with 21CFR820 QSR system and ISO 13485 Preferred
TECHNICAL SKILLS REQUIREMENTS
Required: Strong skills in critical thinking and problem solving, planning and organizing, decision-making
Excellent communication, facilitation and teamwork capabilities
Demonstrated statistics-based data analysis. Familiarity with packages such as JMP, Minitab and Python a plus.
Investigations skills: root cause (5 why, Ishikawa diagrams), warranty estimates, etc.
Project management through JIRA or other equivalent workflow tools
Preferred: Experience supporting review/development of statements of work, schematics, and CAD for new test hardware
Skillset in CAD packages such as SolidWorks or AutoCAD
PHYSICAL POSITION REQUIREMENTS
Candidate will be based in Union City, CA working in an office or laboratory environment.Full timeRegularColleagueZoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at [Register to View] to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at www.Zoetis.com/careers site, or (2) via email to/from addresses using only the Zoetis domain of [Register to View] In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.