Quality Engineer Intern - Manufacturing

Haemonetics • Clinton, PA

1d • $21 - $35

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 At Haemonetics, we make it possible, you make it matter. Our comprehensive portfolio of devices, information management, and consulting services offers blood management solutions for each facet of the blood supply chain — from plasma and blood collectors to hospitals. We believe that through proper blood management, our portfolio of products and services helps to prevent a transfusion for the patient who doesn’t need one and provides the right blood product, at the right time, in the right dose to the right patient who does. Internships projects vary depending on the needs of both the student and the business. Haemonetics Interns are assigned to a meaningful project within the company to acquire a variety of experiences, try different skills, and learn what a future career might offer while also contributing to our innovation agenda by completing business-critical projects and assignments. If you are seeking an internship experience that is challenging and rewarding, Haemonetics is your best next opportunity. PROJECT DESCRIPTION The Quality Engineering team supports daily manufacturing operations in the Clinton, PA (Pittsburgh, PA) facility. The focus of this intern project is to provide support to ensure that the manufactured medical devices meet defined requirements.

Requirements

• Current standing as a Rising Sophomore, Junior, Senior or Graduate student actively enrolled in an accredited Engineering or related field Undergraduate or Graduate program, required.
• Experience with Microsoft Office, including Word, Excel, and PowerPoint
• Strong technical writing, analytical and communication skills
• Detail-oriented with an emphasis on quality work products
• Highly motivated, self-starter with demonstrated experience working with teams

Responsibilities

• Support the Quality Engineering team with process improvement activities; updating and documenting procedures and performing verification steps.
• Learns and applies standards, processes, policies, practices, techniques, and tools throughout the product/system development lifecycle including Standard Operating Procedures (SOP’s) and applicable medical device development protocols under FDA Quality Systems Regulations, CE Marking, and ISO Quality Systems.
• Clearly documents, communicates, and summarizes technical findings and results for status updates, coordination, and recommendations.
• Knowledge of business fundamentals, and leverages creative skills with understanding of policies, procedures, and product/project and operational goals and priorities by executing assigned work with quality, accuracy, and timeliness.

What This Job Offers

• Career Level: Intern
• Education Level: No Education Listed