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Associate QA Engineer (Validation)
full-timeCarrick on Shannon

Summary

Location

Carrick on Shannon

Type

full-time

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About this role

Working at Freudenberg: We will wow your world!

Responsibilities:

  • Understand quality system requirements to support the development, qualification and manufacturing of products to meet internal and external requirements.

  • Utilize statistical analysis tools to support project team.

  • Support creation of Master Validation Plan, validation protocols and reports (IQ/OQ/PQ), quality design reviews deliverables, risk management plan, and all quality related documentation.

  • Assist in and may lead supporting nonconformances, complaints, CAPAs, etc. to resolve quality issues.

  • Support internal and external audits, ensuring quality system compliance.

  • Support Measurement System Analysis (MSA), including Gage R&R, test method validations.

Qualifications:

  • Bachelor's/University degree in Engineering, Chemistry, Biology, or related science/technical field. 

  • 0-3 years’ experience in Medical Device or a related regulated industry.

  • Knowledge of statistical methods, process control, and the use of quality tools such as Design of Experiments (DOE), Failure Mode and Effects Analysis (FMEA), Control Plan, MSA, SPC, as well as GD&T and fixturing. 

  • Demonstrated experience with formal problem-solving methodologies, critical thinking, and deductive skills. 

  • Understanding of ISO standards, particularly ISO 13485, ISO 14001, ISO 14971.  Knowledge of GMP principles and their application in medical device manufacturing, including country-specific regulatory requirements (i.e., 21 CFR 820 in the United States). 

  • Familiarity with design control processes to ensure that design/development, validation, and verification processes align with intended use and performance criteria. 

The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.

Freudenberg Medical Ireland Ltd.

Other facts

Tech stack
Quality System Requirements,Statistical Analysis,Validation Protocols,Risk Management,Nonconformances,Internal Audits,Measurement System Analysis,Gage R&R,Test Method Validations,ISO Standards,GMP Principles,Design Control Processes,Problem-Solving Methodologies,Critical Thinking,Deductive Skills,Quality Tools

About Freudenberg Group

Freudenberg is a global technology group that strengthens its customers and society long-term through forward-looking innovations. Together with its partners, customers and research institutions, the Freudenberg Group develops leading-edge technologies and excellent products and services for about 40 markets and for thousands of applications: seals, vibration control components, technical textiles, filters, specialty chemicals, medical products and the most modern cleaning products.

Strength of innovation, strong customer orientation, diversity, and team spirit are the cornerstones of the Group. The 175-year-old company holds strong to its core values: a commitment to excellence, reliability and pro-active, responsible action.

In 2024, the Freudenberg Group employed more than 52,000 people in some 60 countries worldwide and generated sales of more than €11.95 billion.

Learn more about us and visit our digital home at freudenberg.com and read the stories that make us Freudenberg.​

Visit and follow us at

www.freudenberg.com
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www.youtube.com/FreudenbergGroup

Netiquette

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Team size: 10,001+ employees
LinkedIn: Visit
Industry: Motor Vehicle Manufacturing

What you'll do

  • The Associate QA Engineer will support the development, qualification, and manufacturing of products to meet quality system requirements. Responsibilities include creating validation documentation, supporting audits, and resolving quality issues.

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Frequently Asked Questions

What does a Associate QA Engineer (Validation) do at Freudenberg Group?

As a Associate QA Engineer (Validation) at Freudenberg Group, you will: the Associate QA Engineer will support the development, qualification, and manufacturing of products to meet quality system requirements. Responsibilities include creating validation documentation, supporting audits, and resolving quality issues..

Why join Freudenberg Group as a Associate QA Engineer (Validation)?

Freudenberg Group is a leading Motor Vehicle Manufacturing company.

Is the Associate QA Engineer (Validation) position at Freudenberg Group remote?

The Associate QA Engineer (Validation) position at Freudenberg Group is based in Carrick on Shannon, Connacht, Ireland. Contact the company through Clera for specific work arrangement details.

How do I apply for the Associate QA Engineer (Validation) position at Freudenberg Group?

You can apply for the Associate QA Engineer (Validation) position at Freudenberg Group directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Freudenberg Group on their website.