Supplier Quality Engineer II

Lancesoft; Warsaw (IN); On-site; USD 70,000 - 90,000; Full time

Job summary

Lancesoft in Warsaw, IN is seeking a Supplier Quality Engineer II to join a multi‑department team on a 7+ month contract. You will gather data, assess processes, and ensure products meet established quality standards through audits, inspections, and testing.

You will collaborate with manufacturing, sourcing, and development, apply ISO/QSR requirements, support new product introductions, and help develop budgets while utilizing FMEA, GD&T, CMMs, and optical comparators to verify quality.

Qualifications

• Bachelor's in engineering or equivalent with CQE/CRE preferred.
• 5+ years of experience in a Quality Engineering role, medical device preferred.

Responsibilities

• Gather relevant information to solve quality problems.
• Plan and lead projects with realistic timelines.
• Ensure products conform to established requirements via audits and tests.
• Interact with suppliers, manufacturing, sourcing, and development to enforce quality goals.

Skills

Team collaboration

Quality engineering

Documentation & communication

GD&T & blueprint reading

QSR/ISO regulations

FMEA

CMMs & optical comparators

Education

Bachelor's in engineering

CQE or CRE preferred

Tools

Optical comparators

CMMs

GD&T

Blueprint reading

MS Office

Job description

Title: Supplier Quality Engineer II Location: Warsaw, IN 46580 Duration: 7+ Months (10/19/2026 to 05/28/2027) Duties: Job Summary Responsible for gathering relevant, factual information and data in order to solve quality related problems. Resolve issues by identifying and applying solutions from acquired technical experience and guided precedents. Plan and lead projects by identifying and organizing activities into time dependent sequencing with realistic timelines. Work effectively/ productively with all departments by developing a team atmosphere. 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:

• Evaluating process methods and equipment to meet performance and quality requirements.
• Establishing quality plans for equipment and processes for general and specific product performance needs.
• Monitoring performance of processes to standards.
• Applying ISO and QSR requirements to processes and procedures for Client and outside suppliers.
• Working with suppliers on new product introduction to insurer that quality and performance requirements are fulfilled.
• Assisting Manufacturing, Sourcing and Development in the interpretation and application of regulations.
• Developing and maintaining department and project budgets

Skills: Expected Areas of Competence:

• Ability to work within a team environment and build relationships outside of the department as well as outside the company (suppliers, regulatory agencies, etc.).
• Facilitates team efforts on quality engineering projects.
• Ability to deliver, meet deadlines and have results orientation.
• Able to communicate both orally and in written form to multiple levels of the company.
• Microsoft Office Suite, expert knowledge of blueprint reading and geometric dimensioning and tolerancing, understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methods, and able to use optical comparators and CMMs.
• Knowledge of statistics, process control, and process capability.
• Full working knowledge of all supporting department needs and capabilities, including the ability to discern when inaccurate information is supplied and offer ideas for how to correct it.
• Thorough knowledge base of existing Client products and a basic understanding of competitive products.

Education/Experience Requirements:

Bachelor s in engineering or an alternative Bachelor s degree program with certification as a quality engineer (e.G. CQE). Certification as a quality engineer (e.G. CQE) or the Reliability Engineer Certification (CRE) granted through the American Society of Quality (ASQ) preferred. 5-years experience in a Quality Engineering role and Medical device strongly preferred, or an equivalent combination of education and experience. Combination of education and experience may be considered (in evaluating experience relative to requirements).