Quality Assurance Specialist

Healgen Scientific Limited•Houston, TX

10h•$60,000 - $75,000•Onsite

About The Position

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.

Requirements

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

Nice To Haves

Bilingual individuals that can speak and write Chinese or Spanish.

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.