Supplier Quality Engineer

Aequor; Warszawa; On-site; PLN 122,000 - 207,000; Full time

Job summary

Aequor is seeking a Quality Engineer to oversee quality systems and ensure product conformance for medical device projects. The role involves data analysis, process improvement, and cross-department collaboration to meet ISO/QSR standards.

Responsibilities include planning audits, leading quality initiatives, and coordinating with suppliers to uphold performance requirements while maintaining schedules.

Qualifications

• Bachelor’s in engineering or CQE path.
• ,

Responsibilities

• Gather relevant information to solve quality problems.
• ,

Skills

Team collaboration

Deadline orientation

Written communication

MS Office

Blueprint reading

Geometric dimensioning and tolerancing

QSR/ISO regulations

FMEA

CMMs

Statistics

Education

Bachelor’s in engineering

CQE certification

CRE certification

Tools

Optical comparators

CMM software

Job description

6 months contract with high extension possibility

Warsaw, IN

Pay Rate: $38.92 /Hr on W2

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 our 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

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).