Haemonetics
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We are constantly looking to add to our core talent. If you are seeking a career that is challenging and rewarding, a work environment that is diverse and dynamic, look no further — Haemonetics is your employer of choice.
Job Details
This is a 3rd shift position. Hours are 6:30pm-6:30am. 2-2-3 schedule.
Responsibilities
Accurately and promptly fill out required forms and paperwork documenting inspection and audit functions. Assist in the management of the calibration and environmental monitoring programs.
Audit Product History Records, Sterilization Records, and other documentation as required, in order to prepare product for release.
Carry out specialized testing and investigation as assigned to measure and quantify specific quality issues.
Evaluate and track product returned from the customer per Complaint Handling and Bowl Investigation Procedure.
Perform inspection on incoming raw material per approved procedures. Assist in monitoring supplier quality trends and corrective action.
Perform routine audits of the molding and assembly operation per QCP’s. Work with manufacturing to establish corrective action and assure effectiveness.
Education
H.S. Diploma Required.
Understand all quality requirements (ex. ISO, FDA regulation, etc.) with medical device manufacturing preferred.
Experience
MS Office proficiency (Excel, Outlook) preferred.
Experience in the medical device industry preferred.
Demonstrated written and verbal communication skills.
Strong math skills.
Solid understanding of Quality Systems.
EEO Policy Statement
Seniority level Entry level
Employment type Full-time
Job function Quality Assurance
Industries Hospitals and Health Care and Medical Equipment Manufacturing
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Get AI-powered advice on this job and more exclusive features.
We are constantly looking to add to our core talent. If you are seeking a career that is challenging and rewarding, a work environment that is diverse and dynamic, look no further — Haemonetics is your employer of choice.
Job Details
This is a 3rd shift position. Hours are 6:30pm-6:30am. 2-2-3 schedule.
Responsibilities
Accurately and promptly fill out required forms and paperwork documenting inspection and audit functions. Assist in the management of the calibration and environmental monitoring programs.
Audit Product History Records, Sterilization Records, and other documentation as required, in order to prepare product for release.
Carry out specialized testing and investigation as assigned to measure and quantify specific quality issues.
Evaluate and track product returned from the customer per Complaint Handling and Bowl Investigation Procedure.
Perform inspection on incoming raw material per approved procedures. Assist in monitoring supplier quality trends and corrective action.
Perform routine audits of the molding and assembly operation per QCP’s. Work with manufacturing to establish corrective action and assure effectiveness.
Education
H.S. Diploma Required.
Understand all quality requirements (ex. ISO, FDA regulation, etc.) with medical device manufacturing preferred.
Experience
MS Office proficiency (Excel, Outlook) preferred.
Experience in the medical device industry preferred.
Demonstrated written and verbal communication skills.
Strong math skills.
Solid understanding of Quality Systems.
EEO Policy Statement
Seniority level Entry level
Employment type Full-time
Job function Quality Assurance
Industries Hospitals and Health Care and Medical Equipment Manufacturing
#J-18808-Ljbffr