Are you interested in working at an innovative Medical Device/Pharmaceutical company?

Role Description

This role has primary responsibility for confirmation that medical devices and combination products meet their intended function. This includes the development of data through engineering studies that informs new product development as well as test reports that support product submissions. The candidate will work within a team environment to solve problems and utilize best engineering practices and techniques for root cause and statistical analysis. This work entails defining test methods, developing protocols, performing data analysis, and writing reports in compliance with corporate procedures.

Responsibilities

• Partner with Systems engineers in defining product requirements such that they are verifiable
• Development of test fixtures, test methods, and performance of Test Method Validation activities
• Coordinate with internal and external partners and suppliers to procure test samples and manage conditioning and accelerated aging studies
• Ensure integrity and compliance of data according to Standard Operating Procedures
• Develop Design Verification Plans including test strategy
• Utilize technical writing and statistical data analysis skills to write protocols and reports
• As necessary, conduct root cause analysis and derive recommendations based on analysis of data
• Translate inspections and tests methods into component and product specifications
• Engineering testing

Qualifications

• B.S. in Engineering discipline and 0 to 3 years related experience, preferably in Mechanical/Chemical/Biomedical Engineering.
• Laboratory testing experience.
• Familiarity with ISO standard test methods and related test instrumentation preferred. Excellent analytical and communication skills required. Ability to work and solve problems in team environment. Technical writing skills are required for protocol and report writing.
• Strong statistical analysis skills with Minitab, preferred.
• Experience writing Design Verification and Validation Plans, Protocols, and Reports, preferred.
• Experience performing test method validations, TMV, Preferred
• Green Belt and/or Black Belt Certification a plus
• Manufacturing operation experience a plus

Physical/Mental Requirements

Physical requirements include walking, standing, and performing analysis including protocol and report writing. Includes hands-on test method development.

Location: Lake Forest, IL

Employment Type: W2 employee

Benefits:

• Choice of medical, dental, and vision plans.
• Paid vacation time.
• Competitive hourly rate.

This is a great opportunity and we're looking to fill this role with the right person. If you are ready to embark on an amazing new career opportunity, APPLY RIGHT NOW!

About Ventura Solutions:

Ventura Solutions is a rapidly growing medical device and pharmaceutical staffing, consulting, and training firm. Our extensive industry expertise in medical device, pharmaceutical, and combination products along with an exceptional talent pipeline make us a top choice for a wide range of projects. We also offer great benefits which enable us to attract and retain top talent in the medical device, pharmaceutical, and combination products space. For more information and other job opportunities visit us at ventura-solutions.com

Equal Opportunity Employer Minorities/Women/Veterans/Disabled

 

Posted On: Friday, May 13, 2022