Medical Device Post Market QC Associate
Stratacuity: Proven Scientific Placement, Acton, MA, United States
Overview
Our client is looking for a Medical Device Post Market QC Associate to support medical device investigations. In this role, you will use your prior background in quality compliance to adhere to processing standards as you receive and unpack returned medical devices.
Responsibilities
Operating safely while consistently following laboratory and quality protocols
Entering data related to each return accurately and promptly
Checking information against lot acceptance records and DHRs to support investigations
Creating, maintaining, and reviewing quality records in a manner consistent with the company's quality system
Maintaining audit readiness
Qualifications
Education: High School Diploma or higher education
1+ year of direct experience in receiving, material handling, or inspection roles within a quality-regulated environment
Ability to work in an environment where you alternate between sitting and standing
Ability to lift ~5 pounds, and push/pull upto 50 pounds
Ability to work onsite for full-time regular hours Monday-Friday
Preferences
Experience working in the medical device industry or working in a biohazard/lab role
Proficiency with MS office tools
Ability to generate and maintain records that are accurate and organized
#J-18808-Ljbffr
Our client is looking for a Medical Device Post Market QC Associate to support medical device investigations. In this role, you will use your prior background in quality compliance to adhere to processing standards as you receive and unpack returned medical devices.
Responsibilities
Operating safely while consistently following laboratory and quality protocols
Entering data related to each return accurately and promptly
Checking information against lot acceptance records and DHRs to support investigations
Creating, maintaining, and reviewing quality records in a manner consistent with the company's quality system
Maintaining audit readiness
Qualifications
Education: High School Diploma or higher education
1+ year of direct experience in receiving, material handling, or inspection roles within a quality-regulated environment
Ability to work in an environment where you alternate between sitting and standing
Ability to lift ~5 pounds, and push/pull upto 50 pounds
Ability to work onsite for full-time regular hours Monday-Friday
Preferences
Experience working in the medical device industry or working in a biohazard/lab role
Proficiency with MS office tools
Ability to generate and maintain records that are accurate and organized
#J-18808-Ljbffr