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A high school diploma or GED with 1+ years of experience in a medical device or manufacturing environment is required, or equivalent combination of education and experience. Additional desired qualifications include background in regulated industries like medical device or pharmaceutical, strong communication skills, attention to detail, proficiency with MS Office, and excellent organizational skills.
The role requires on-site work. Candidates must have willingness and ability to work on site in general office, laboratory, and cleanroom environments.
This information is not specified in the job description.
The role involves working in general office, laboratory, and cleanroom environments with potential exposure to blood-borne pathogens, some lifting up to 50-100 pounds, and occasional ladder climbing.
Strong candidates will have experience in medical device or regulated manufacturing, strong communication and organizational skills, attention to detail, and proficiency with MS Office tools, along with the ability to handle maintenance, troubleshooting, and quality system adherence.
Develops medical devices for vascular conditions
Penumbra Inc. specializes in creating medical devices aimed at treating neurovascular and peripheral vascular conditions. Their products, such as the Penumbra System and the Indigo System, are designed for use in hospitals and clinics, helping healthcare professionals address issues like stroke and other vascular diseases. These devices work by providing advanced tools for interventions in neurology and vascular surgery, allowing for effective treatment options. Unlike many competitors, Penumbra focuses specifically on these specialized areas, ensuring their products are tailored to the needs of medical professionals in these fields. The company's goal is to continuously improve and innovate their medical devices to enhance patient care and support healthcare providers in delivering effective treatments.