Top 6 Quality engineer medical device Jobs in Topeka In

Quality Engineer I - Warsaw
Tecomet —Warsaw, IN
- $70,000 - $80,000 a year
- Microsoft Excel
- Microsoft Outlook
- Mid-level
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9d
Quality Engineer I
Tecomet —Warsaw, IN
- Microsoft Excel
- Microsoft Outlook
- Mid-level
Quick Apply
Manufacturing Controls Engineer - Sturgis, MI Plant
Abbott Laboratories —Sturgis, MI
- $61,300 - $122,700 a year
- Full-time
- Engineering
- Mid-level
- Children
- Paid holidays
- Health insurance
Manufacturing Engineer
AMETEK, Inc. —Pierceton, IN
- $100,000 - $115,000 a year
- Anatomy knowledge
- 7 years
- Office
Manufacturing Engineer
Avalign Technologies Inc —Warsaw, IN
- Full-time
- Microsoft Outlook
- Customer service
- Bachelor of Science
- AD&D insurance
- Paid holidays
Quick Apply
Senior Sterile Packaging Engineer
Red Star —Larwill, IN
- Full-time
- 3 years
- Mentoring
- Senior level
- Paid holidays
- Health insurance
Quick Apply
13d

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Quality Engineer I - Warsaw

Tecomet -
Warsaw, IN

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Job Details

$70,000 - $80,000 a year
9 days ago

Qualifications

Good documentation practices (GDP)
GMP
Biomedical regulatory compliance
FDA regulations

Full Job Description

Quality Engineer I

Position Summary

The Quality Engineer I will interact with team members to ensure compliance and internal and external customer requirements are met, with focus on quality engineering. This will be accomplished within Tecomet's principles of continuous improvement, customer driven innovation and a win first culture, while meeting company financial and other performance metrics.

Principle Responsibilities

Maintaining applicable quality system, environmental, and FDA requirements/certifications.
Facilitate operator owned quality program.
Supporting the MRB and RMA processes.
Work with team members and support manufacturing/operations to solve quality, cost and schedule issues.
Prepare FMEA's, controls plans, quality plans, PPAP.
Coordinate process validations and reduce dependence on inspection.
Generating applicable quality metric reports; cost of quality, management by facts.
Investigate customer complaints including associated actions including CAPA, deviations, and complaint responses.
Special projects as assigned by quality management.
Must demonstrate a working knowledge of standard manufacturing operations, FDA and ISO regulations.
Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) requirements.
Standard problem-solving techniques.
Applies statistical and Six Sigma concepts and techniques.
Works with Internal and External Customers.
Participates in audits and inspections.

Qualification Requirements

Credentials/Experience:

Bachelor's Degree in Engineer or related field. Or a minimum of 4 years' experience within the Medical Device Industry, and Certification (ASQ CQE or CMQ/QE)

Experience/Educational/Training Preferred:

ASQ CQE or CMQ/QE preferred
2 years' experience in quality within medical device manufacturing industry preferred
ISO 13485, FDA 820 and customer interaction experience preferred

Knowledge, Skills, and Abilities:

Manufacturing operations – forging and/or machining.
Measuring devices.
Quality Systems.
Regulations – FDA, GMP and ISO.
Blueprint reading.
GD&T.
Metrology.
Problem solving and 8D.
Math skills (algebra, trigonometry) skills.
Microsoft office (Word, Excel, Outlook, PowerPoint).
Minitab.

Other Requirements

Work Environment

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Physical Requirements

The employee could frequently be required to walk; use hand to finger, handle, or feel; reach with hands and arms and talk or hear. The employee could be required to sit; climb or balance and stoop, kneel, crouch, or crawl. The employee could occasionally lift and or move up to 50 pounds. Specific vision abilities required by the job could include close vision, distance vision, peripheral vision and ability to adjust focus.

Travel Requirements

Up to 10%

Americans with Disabilities Act (ADA): Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

The statements herein are intended to describe the general nature and level of work being performed by employees and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of the Company.

Pay Transparency In order to support the Fair Compensation Strategy by the US Govt., HR Dept., clients are required to adhere to "Pay Transparency Law"; in the impacted states; that have mandated the employers to list the salary ranges in Job advertisements or postings for job opportunities and Job promotions.

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quality engineer medical device jobs in topeka in

Quality Engineer I - Warsaw

Quality Engineer I

Manufacturing Controls Engineer - Sturgis, MI Plant

Manufacturing Engineer

Manufacturing Engineer

Senior Sterile Packaging Engineer

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