At Tactile Medical, we specialize in developing at-home therapy devices to treat lymphedema, chronic venous insufficiency and respiratory illnesses. At Tactile Medical, we specialize in developing at-home therapy devices to treat lymphedema, chronic venous insufficiency and respiratory illnesses. The Quality Technician I is responsible for assisting the Quality department focusing on post market surveillance reporting

Requirements

This position will specialize in documenting, evaluating, dispositioning, investigating product reports and identifying field complaints. This individual will also perform inspection activities including evaluating product failures and defects resulting from incoming inspection. Accountabilities &

Other related duties as assigned

and conditions. Below is the starting salary or hourly range for this position, although offers may differ based on the candidate's location, job-specific knowledge, skills and experience. US Pay Range $23.

89 — $31.35 USD To learn more about our Privacy Statement follow this link - https://tactilemedical.com/privacy-statement/ To learn more about our California Privacy Notice follow this link - https://tactilemedical.

com/california-privacy-notice/

Responsibilities

Post Market Surveillance Support the complaint handling process by evaluating returned product failures to determine the cause of customer complaints Prepare technical reports of findings using trend analysis and other statistical methods Repair and/or replace components to reprocess devices for future use Perform experimental testing as needed to assist with root cause analysis Product Acceptance & Investigations Assist with performing analysis, inspection, troubleshooting, and testing of products or components identified as non-conforming during incoming, in-process and final inspection Participate in the non-conforming material reporting process; including, but not limited to, documenting non-conformance description, assigning a control number, and evaluating to determine cause of the non-conformance General

Identify areas of improvement and participate in continuous improvement projects Perform decontamination of returned products prior to evaluation Perform all job duties while adhering to HIPAA

Qualifications

Required: 1+ years’ experience in the medical device industry AA degree or equivalent work experience in related discipline Preferred: Experience with electro-mechanical devices ASQ Quality Technician certification or equivalent Experience using an ERP system Knowledge & Skills Proficient with Microsoft Office tools, including Word, Excel, PowerPoint, and Outlook Strong organization, time management, and communication skills Ability to follow instructions, procedures, and good documentation practices Hands-on troubleshooting and product evaluation skills Self-starter who can work independently and collaboratively Our total

Compensation

package includes medical, dental and vision

Benefits

, retirement

, employee stock purchase plan, paid time off, parental leave, family medical leave, volunteer time off and additional leave programs, life insurance, disability coverage, and other life and work wellness

and discounts.

may be subject to generally applicable eligibility, waiting period, contributions, and other