Quality Assurance Specialist
Healgen Scientific
Invite-only right now: save jobs, track applications, build tailored resumesAlready have an account? Log in
- Pay
- $60K to $75K
- a year
- Location
- Houston, TX
- Work style
- On-site
- Job type
- Full time
- Posted
- Oct 8
- 12 days ago
Career path
See where this role leads
Jigup maps the next three moves from a job like this one, with the titles and the skills each step asks for.
About the company
Healgen Scientific
Medical devices · 51 to 200 employees
What you'll do
- 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.
What you need
- 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.
- Education: a bachelor's degree
Key skills
FDA guidelinesISO 13485 regulationsroot cause analysesbasic statistical analysiswritten and spoken EnglishChineseSpanish
Keywords for your resumePro
The words this employer's screening is likely to look for.
This job lists resume keywords
The terms this posting uses, pulled out so you can mirror them in your resume. Jigup Pro members see the list on the job board.
See full description on company page, apply now
Read the full posting here
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.
Duties and responsibilitiesWork 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.
QualificationsHave 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.