Job Description
A client in the medical device industry is seeking a Sr. Mechanical Engineer to join their Research + Development team in support of a remediation project. The ideal resource will have a strong mechanical engineering background with specific experience working with Solidworks CAD software, developing test methodologies, and running the design verification process. Day to day activities will include developing test methodology as the team moves into the execution portion of their remediation project and involves interfacing with Technicians and DQA Engineers. The role will be a 5-month contract with possible extensions until integration work is concluded and hybrid 3 days per week in Valencia, CA requiring the resource to be onsite in their machine shop with the R+D team.
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Required Skills & Experience
• Bachelor’s Degree in Mechanical Engineering or related field
• 5+ years of Mechanical Engineering experience
o Preferred experience working within Research + Development
• Experience owning Test Method Development
• Proficiency in CAD software, specifically Solidworks/Minitab modelling + updating drawings
• Design Verification + Validation experience, working with DHF
• Strong written + verbal communication skills
Nice to Have Skills & Experience
• Medical Device industry experience
• Experience working within FDA Quality System Regulations and ISO 13485
• Experience supporting remediation projects
Benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.