As a part of the team, you will be contributing to each of our core beliefs: Empowerment, Innovation, Speed & Purpose, Teamwork & Collaboration, Growth, and Fun. You will be empowered to ensure we are producing high quality products that meet the standards of our regulatory bodies and our customers.

Quest Medical, Inc. is a US based manufacturer that develops and manufactures sterile medical devices for a variety of medical markets. Those markets include cardiac surgery, ophthalmic surgery, oncology, IV fluid, and anesthesia delivery. Our company culture is very diverse and the average tenure for our employee population is 7+ years. If you are looking for a stable and successful company where your voice will be heard, Quest is the place to be.

Position Title:

Quality Engineering Intern – 14 week Summer Program

Reports to:

Quality Engineering Manager

Department:

Quality

Location:

Allen, TX 75002

Summary:

Learn quality management operations and quality controls methods in manufacturing.  This candidate will work in collaboration with the Quality Engineering team on various projects.  He or she will make detailed observations, analyze data, and interpret results.  Candidate will prepare quality management documentation, prepare technical reports, and conduct quantitative analyses.

Requirements:

• Currently enrolled student majoring in Biomedical Engineering or related field that has completed freshman year courses.
• Minimum 3.0 GPA
• Good verbal, written, and interpersonal communication skills for effective interface with all contacts.
• Ability to work effectively with others and be a participative team player.
• Good organizational ability and attention to detail.
• Authorized to work in U.S.
• Comfort with group/individual presentations.
• Intermediate knowledge and experience in Microsoft Office programs, including Word, Excel, PowerPoint and Outlook.

Duties:

• Adhere to and ensure compliance with Quality System objectives (SOPs, work instructions, drawings, technical documentation, current Good Manufacturing Practices (cGMPs)).
• Collect, analyze, trend and communicate quality data.   Self-checks work for completeness and accuracy.
• Support improvement initiatives in the quality management system throughout organization (NCMRs, Complaints, CAPAs, ECOs).
• Assist the Quality Engineer with Corrective and Preventive Action (CAPA) activities (root causes, investigations, implementations of corrective actions and completion).
• Write and revise quality systems documentation (SOPs, work instructions, test procedures)
• Perform testing under guidance to support validation activities, component qualification activities, IQ/OQs, test method validations, and Gage R&R studies.
• Creates Engineering Change Order documentation under the guidance of Quality Engineer.
• Works under general supervision of the Quality Engineer, QMS Manager, and / or other personnel as assigned.  Relies on instructions and pre-established guidelines to perform the functions of the job. Assumes additional responsibilities as necessary at the discretion of QA.

An Equal Opportunity Employer