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Quality Manager

  • Quality Manager job type Posted on: Nov 05, 2026
  • Quality Manager experience level TekWissen LLC
  • Quality Manager employment type Warsaw, Indiana
  • Quality Manager salary Salary: $50 per hour
  • Quality Manager employment type Onsite
  • Quality Manager salary Full-time

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Job Title :

Quality Manager

Job Type :

Full-Time

Job Location :

Warsaw Indiana United States

Remote :

No

Jobcon Logo 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 Manager
Location: Warsaw, IN 46580
Duration: 12 Months
Job Type: Temporary Assignment
Work Type: Onsite
a { text-decoration: none; color: #464feb; } tr th, tr td { border: 1px solid #e6e6e6; } tr th { background-color: #f5f5f5; }
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 and 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 established standards.
  • Applying ISO and QSR requirements to processes and procedures for client and outside suppliers.
  • Working with suppliers on new product introduction to ensure 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 (i.e. KSAs)
  • 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 demonstrate results orientation.
  • Able to communicate both orally and in written form to multiple levels of the company.
  • Microsoft Office Suite proficiency.
  • Expert knowledge of blueprint reading and geometric dimensioning and tolerancing (GD&T).
  • Understanding of QSR/ISO regulations.
  • Design assurance knowledge.
  • FMEA (Failure Mode and Effects Analysis).
  • Product testing methods.
  • Ability 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 correction.
  • Thorough knowledge base of existing client products and a basic understanding of competitive products.
Education: Education / Experience Requirements
  • B.S. in Engineering or an alternative Bachelor's degree program with certification as a Quality Engineer (e.g., CQE).
  • 5 7 years of experience in a Quality Engineering role.
  • Medical device industry experience strongly preferred.
  • Equivalent combination of education and experience may be considered.
  • Combination of education and experience may be considered when evaluating experience relative to requirements.
TekWissen Group is an equal opportunity employer supporting workforce diversity.

Jobcon Logo Position Details

Posted:

Nov 05, 2026

Reference Number:

52391-12690

Employment:

Full-time

Salary:

$50 per hour

City:

Warsaw

Job Origin:

CIEPAL_ORGANIC_FEED

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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 Manager
Location: Warsaw, IN 46580
Duration: 12 Months
Job Type: Temporary Assignment
Work Type: Onsite
a { text-decoration: none; color: #464feb; } tr th, tr td { border: 1px solid #e6e6e6; } tr th { background-color: #f5f5f5; }
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 and 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 established standards.
  • Applying ISO and QSR requirements to processes and procedures for client and outside suppliers.
  • Working with suppliers on new product introduction to ensure 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 (i.e. KSAs)
  • 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 demonstrate results orientation.
  • Able to communicate both orally and in written form to multiple levels of the company.
  • Microsoft Office Suite proficiency.
  • Expert knowledge of blueprint reading and geometric dimensioning and tolerancing (GD&T).
  • Understanding of QSR/ISO regulations.
  • Design assurance knowledge.
  • FMEA (Failure Mode and Effects Analysis).
  • Product testing methods.
  • Ability 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 correction.
  • Thorough knowledge base of existing client products and a basic understanding of competitive products.
Education: Education / Experience Requirements
  • B.S. in Engineering or an alternative Bachelor's degree program with certification as a Quality Engineer (e.g., CQE).
  • 5 7 years of experience in a Quality Engineering role.
  • Medical device industry experience strongly preferred.
  • Equivalent combination of education and experience may be considered.
  • Combination of education and experience may be considered when evaluating experience relative to requirements.
TekWissen Group is an equal opportunity employer supporting workforce diversity.

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