Quality Engineer I

TekWissen LLC; Warsaw (IN); On-site; USD 55,000 - 75,000; Part time

Job summary

TekWissen Group in Indiana is seeking a Quality Engineer I for a 6-month onsite assignment in Warsaw. The role focuses on ensuring products meet established requirements through audits, inspections, and testing.

You will collaborate with diverse teams and suppliers to implement quality goals, formulate procedures, and support corrective actions. This entry-level position offers exposure to ISO standards and quality systems within a medical device context.

Qualifications

• B.S. in engineering or equivalent with CQE certification.
• CQE certification and medical device/orthopedic experience preferred.

Responsibilities

• Formulates procedures, specifications, and standards for client products and processes.
• Develops and implements corrective/preventative action plans.
• Collects and analyzes data for gauge and product evaluation.
• Identifies critical personnel, gauges, procedures, and materials needed for new products.
• Ensures suppliers have information and facilities to deliver quality products.

Skills

Teamwork

Deadline driven

Communication

Growth mindset

MS Office

Blueprint reading

GD&T

QSR/ISO regulations

Design assurance

FMEA

Product testing methods

Optical comparators

CMMs

Education

B.S. in engineering

CQE certification

Tools

CMMs

Optical comparators

Job description

Overview:

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. Client designs, develops, manufactures and markets orthopedics products, including knee, hip, shoulder, elbow, foot and ankle artificial joints and dental prostheses. client has operations in more than 40 countries around the world

Job Title: Quality Engineer I

Work Location:

Warsaw, IN, 46582

Duration: 6 Months

Job Type: Temporary Assignment

Work Type: Onsite

Job Description:

• The Quality Engineer I is an entry level position responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities.
• Interacts with many different functional departments, suppliers, and experts outside client to implement client Quality goals.

Principal Duties and Responsibilities:

• Formulates procedures, specifications, and standards for client products and processes.
• Develops and implements corrective/preventative action plans.
• Collects and analyzes data for gauge and product evaluation.
• Identifies critical personnel, gauges, procedures, and materials needed for the completion of new products.
• Ensures that suppliers have necessary information and facilities to deliver quality products to client.

Expected Areas of Competence (i.e., knowledge, skills and abilities):

• Ability to work within a team environment and build relationships outside of the department as well as outside the company (suppliers, regulatory agencies, etc.).
• Ability to deliver, meet deadlines and have results orientation.
• Able to communicate both orally and in written form to multiple levels of the company.
• Demonstrates characteristics of high potential for future development opportunities.
• Microsoft Office Suite
• Basic knowledge of blueprint reading and geometric dimensioning and tolerancing, basic understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methods, and are able to use optical comparators and CMMs.

Education/Experience Requirements:

• B.S. in engineering or an alternative Bachelor's degree program with certification as a quality engineer (e.g. CQE).
• Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred.

TekWissen Group is an equal opportunity employer supporting workforce diversity.