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:

Process Engineering Intern – 14 week Summer Program

Reports to: 

Advanced Process Engineering Manager

Department:

Advanced Process Engineering

Location:

Allen, TX 75002

Summary:

Supports daily manufacturing operations and activities associated with process improvement, validation, QA systems, and technology/product development.

Qualifications:

• Working towards an undergraduate or graduate degree in a relative Engineering program.
• Ability to communicate effectively both written and orally.
• Computer literate and possess ability to use major software tools.

Responsibilities:

• Perform duties and responsibilities under the direct supervision and leadership of the Process Engineering Manager and/or senior engineering personnel.
• Identify, justify and implement equipment upgrades, new product and process technologies, and process improvements.
• Understand basic requirements of design control during product and/or process development projects.
• Understand quality system requirements of customers, FDA, QSR, and other regulatory agencies, and use quality tools to improve processes and products within those standards.
• Perform analysis of data and reports results in a technical report.
• Perform root cause analysis and recommends resolution of problems associated with products, manufacturing processes, and customer complaints.
• Perform design verification and validation activities which meet all necessary requirements of a project, including drafting qualification documents ranging from equipment qualification to product validation.
• Manage complaint investigation activities for required product lines consisting of failure investigation, root cause analysis, and corrective and preventative action implementation for complaint issue.
• Draft engineering change order reports and non-conforming material reports.
• Support, coordinate, and/or lead projects requiring cross-functional team participation to meet project goals.
• Possess technical writing, project management and fundamental problem-solving skills.
• Able to apply advanced mathematical concepts and statistical analysis.
• Provides support role for senior engineering personnel in all aspects of medical device manufacturing engineering.

An Equal Opportunity Employer