We’re looking for a passionate quality engineer to validate new equipment and processes, perform product inspections, record reviews, and assist with product investigations.
You may also evaluate manufacturing processes for improvements and optimization.
You will develop validation and quality plans for new or changing equipment, and/or processes and assist with their execution and documentation, execute product sampling and inspections, perform QA reviews of manufactured products and quality records and assist with product Technical Support, supporting investigations and documentation.
Bachelor’s degree in life science or engineering discipline
At least 3 years’ experience as a Quality Engineer or equivalent position in a quality department of medical device or similarly cGMP/ISO regulated industry
Previous experience with writing and executing validation plans
Experience with electronic Document Management system is desirable
Excellent organizational skills, attention to detail, ability to manage time and prioritize
Attention to detail is fundamental to this position
Ability to think proactively, troubleshoot, investigate and improve systems
Excellent communication and interpersonal skills, able to interact with people at all levels of the organization
Check us out at www.ivWatch.com or watch a product demonstration here.
If you think you have what it takes to join the dynamic team at ivWatch, please email your information to firstname.lastname@example.org.