Quality Assurance Technician

Haemonetics • Clinton, PA

3d

About The Position

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 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. 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 Throughout our history, we have earned a solid reputation for product innovation, technical expertise, and operational excellence. Today, our products, internal research and development, marketing partnerships, and product acquisitions reflect our unwavering commitment to provide safe and available blood for patient transfusions and for use in pharmaceuticals. We rely on our talented global workforce to help us achieve our mission of providing innovative medical devices that advance the safety, quality, and availability of the world's blood supply. To achieve our business goals and objectives, we are committed to attracting and retaining the best and brightest talent while offering a challenging, dynamic, and exciting work environment that offers professional growth and development.

Requirements

• H.S. Diploma Required.
• Strong math skills
• Solid understanding of Quality Systems

Nice To Haves

• Understand all quality requirements (ex. ISO, FDA regulation, etc.) with medical device manufacturing preferred.
• MS Office proficiency (Excel, Outlook) preferred
• Experience in the medical device industry preferred
• Demonstrated written and verbal communication skills

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.
• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED
• Number of Employees: 1,001-5,000 employees