Product Release Quality Assurance Associate or Technician (1st Shift)

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At MicroPort we relentlessly strive to master every detail of our medical solutions with the purpose of prolonging and reshaping the lives of patients everywhere. We welcome motivated and talented people who want to join our dynamic and inclusive company working together to deliver meaningful medical order to accomplish this we hold true to our core values of Quality Integrity Accountability Efficiency Innovation Aspiration Dedication & Collaboration. Come and join Team MicroPort!

Why Youll Love MicroPort

You will find our team atmosphere challenging and addition to working with a world-class team receiving a competitive base salary and bonus opportunities our U.S. employees also enjoy the following benefits: Medical Dental Vision Maternity Leave Life Insurance Short-Term Disability Long-Term Disability Bereavement 401(k) (up to 4% match with vesting from day 1) PTO Employee Assistance Program Education more! At MicroPort we care about our employees and encourage them to make healthy lifestyle choices and embrace wellness opportunities to maintain their very best health and wellbeing.

Overall Summary

As Product Release Quality Assurance Associate or Technician you will perform documentation review to all device history associated data and documentations prior to releasing product. You will ensure products are not available for release until ambiguities and errors are resolved. Authorized person(s) shall issue the product release form as required and approve the release of the finished product while remaining independent of other functions such as but not limited to production and inspection.

This is a 1st shift position: 7:00am-3:30pm Monday-Friday

Your duties will include:

1. Assure inspection is performed in accordance with FDA ISO and other applicable regulations / guidelines.
2. Follow written instructions with engineering-based content.
3. Apply attention to detail in documentation.
4. Interface with peers engineers and Regulatory auditors.
5. Accurately record data results to ensure proper segregation of accepted and rejected products.
6. Operate under the direction of QC Management team.
7. Develop update and maintain Device History Record database
8. Provide Certificate of Conformance (CoC) upon request

Other Duties: Please note this job description is not designed to cover or contain a comprehensive listing of activities duties or responsibilities that are required of the employee for this job. Duties responsibilities and activities may change at any time with or without notice.

About You

We might be a great match if you have:

Ability to follow instructions both written and oral.

Ability to work in a team environment.

Professional communication skills.

A working knowledge of basic computer skills

Ability to apply skills in a manner to ensure proper decisions for acceptance or rejection of goods is imperative.

Database management knowledge

Ability to work independently

YOUR EDUCATION

Required: High School Diploma or GED

Preferred: High School Diploma

YOUR EXPERIENCE

Associate: No related experience required

Technician: One year of related experience required

Visual acuity requirements apply to the role including peripheral color and depth perception.

For internal reference the Associate is a level H2 and the Technician is a level H3.

Required Experience:

IC