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Quality Assurance Specialist

  • Quality Assurance Specialist job type Posted on: Nov 05, 2026
  • Quality Assurance Specialist experience level Healgen Scientific Limited
  • Quality Assurance Specialist employment type Houston, Texas
  • Quality Assurance Specialist employment type Onsite
  • Quality Assurance Specialist salary Full-time

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Job Title :

Quality Assurance Specialist

Job Type :

Full-Time

Job Location :

Houston Texas United States

Remote :

No

Jobcon Logo Job Description :

Job Description

Job Description

The ideal QA Specialist candidate would have a strong understanding of FDA guidelines and ISO 13485 regulations to ensure compliance and uphold product quality standards. The Quality Assurance Specialist will play a critical role in the development, implementation, and maintenance of quality assurance processes and systems to support the manufacturing and distribution of medical devices.

This is a fulltime in office position located in the Houston, TX area.

Duties and responsibilities
  • Work with a cross-functional team to ensure all documents are properly stored and archived.
  • Support and track Quality related events such as CAPAs, SCARs, Non-conformances, Deviations, Reworks and Customer Complaints. 
  • Supports investigations and root cause analyses.
  • Facilitate document control and change control process by initiating and completing CO’s.  
  • Coordinate with process owners to update procedures and draft documentation as required. 
  • Ensure completed documentation meets internal quality standards.
  • Data entry and basic statistical analysis.
  • Support during Internal and External regulatory audits.
  • Inspection of raw material and in-process and finished products.
  • Assist manufacturing with batch release and other relevant documentation.
  • Assist with post-market monitoring of the company’s products.
  • Creates and keeps track of training events to ensure employee training records are up to date and compliant.
  • Support with supplier evaluations and maintenance of the Approved Supplier List.
  • Assist in other duties.

 

Qualifications
  • Have at least 2 years of relevant experience and a relevant bachelor’s degree OR at least 5 years of relevant experience without a degree, preferably in the Medical Device or Pharmaceutical industry.
  • Be able to work with a cross-functional team on an international stage
  • Be able to communicate effectively in written and spoken English
  • Be able to troubleshoot as necessary
  • Be able to prioritize tasks effectively
  • Show initiative and be proactive in their day-to-day tasks
  • Preference for bilingual individuals that can speak and write Chinese or Spanish.

Jobcon Logo Position Details

Posted:

Nov 05, 2026

Reference Number:

c7ab0d04

Employment:

Full-time

City:

Houston

Job Origin:

ziprecruiter

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Job Description

Job Description

The ideal QA Specialist candidate would have a strong understanding of FDA guidelines and ISO 13485 regulations to ensure compliance and uphold product quality standards. The Quality Assurance Specialist will play a critical role in the development, implementation, and maintenance of quality assurance processes and systems to support the manufacturing and distribution of medical devices.

This is a fulltime in office position located in the Houston, TX area.

Duties and responsibilities
  • Work with a cross-functional team to ensure all documents are properly stored and archived.
  • Support and track Quality related events such as CAPAs, SCARs, Non-conformances, Deviations, Reworks and Customer Complaints. 
  • Supports investigations and root cause analyses.
  • Facilitate document control and change control process by initiating and completing CO’s.  
  • Coordinate with process owners to update procedures and draft documentation as required. 
  • Ensure completed documentation meets internal quality standards.
  • Data entry and basic statistical analysis.
  • Support during Internal and External regulatory audits.
  • Inspection of raw material and in-process and finished products.
  • Assist manufacturing with batch release and other relevant documentation.
  • Assist with post-market monitoring of the company’s products.
  • Creates and keeps track of training events to ensure employee training records are up to date and compliant.
  • Support with supplier evaluations and maintenance of the Approved Supplier List.
  • Assist in other duties.

 

Qualifications
  • Have at least 2 years of relevant experience and a relevant bachelor’s degree OR at least 5 years of relevant experience without a degree, preferably in the Medical Device or Pharmaceutical industry.
  • Be able to work with a cross-functional team on an international stage
  • Be able to communicate effectively in written and spoken English
  • Be able to troubleshoot as necessary
  • Be able to prioritize tasks effectively
  • Show initiative and be proactive in their day-to-day tasks
  • Preference for bilingual individuals that can speak and write Chinese or Spanish.

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