Haemonetics Corp
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 Seeking a highly motivated individual with exceptional attention to detail and a strong commitment to accuracy
Hours are 2:30pm-11:00pm ( Monday- Friday)
Responsibilities
Accurately and promptly fill out required forms and paper work 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.
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
#J-18808-Ljbffr
Job Details Seeking a highly motivated individual with exceptional attention to detail and a strong commitment to accuracy
Hours are 2:30pm-11:00pm ( Monday- Friday)
Responsibilities
Accurately and promptly fill out required forms and paper work 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.
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
#J-18808-Ljbffr