What are the responsibilities and job description for the Quality Assurance Associate- Temporary position at Nventric, Inc.?
Date posted: October 2, 2025
Pay: From $26.00 per hour
Job Type: Full-Time, Temporary
Job Description:
Position Summary: The Quality Assurance Associate's role is to support the company’s Quality System maintenance as well as assist on QA/QE tasks as required. This is essential as it ensures the activities of the company are performed in full compliance with Nventric’s quality system, ISO 13485, EU MDR, FDA QSR, Korea Medical Device Act, and other appropriate international Quality System requirements.
Duties & Responsibilities:
- Support development and implementation of Nventric’s quality policies and practices
- Support maintenance of Quality Management System in full compliance with ISO 13485 and FDA QSR
- Support in document design reviews, training plans, internal/external audits, etc., as necessary
- Ensure design documentation aligns with regulatory compliance requirements.
- Perform inspection activities from filling out forms, inspecting components based on technical ndrawings, to recording data.
- Support Inspections regarding Receiving, In-Process Quality Control, Finished Goods Quality Control, and other material inspections as necessary.
- Support the traceability and inventory tracking of materials transferred from Manufacturing / QC Inspections to Inventory.
- Support regulatory compliance and quality plans and strategies in concert with affected functional areas
- Support Quality activities related to maintaining DCO and inspection of goods.
- Monitor FDA and other agency laws and regulations, and provide regulatory interpretation and impact analysis on company projects
- Review product development and clinical protocols to assure collection of appropriate data for regulatory submissions and regulatory compliance
- This includes use of appropriate standards, experimental designs, evaluation criteria, and statistical rationale
- Coordinate and prepare, or support the preparation of regulatory submissions, including documentation required for registration of products in the markets to which Nventric distributes their devices
- Proactively champion quality issues where applicable in company-wide activities
- Collaborate with R&D to determine the quality assurance strategy from product inception to product launch
- Support Supplier QA, Manufacturing QA, and Design Assurance, as necessary per QA/QE.
- Other duties as assigned.
Qualifications:
- Bachelor’s degree or equivalent, relevant professional experience in a regulated industry preferred (medical device experience preferred)
- Early and late stage development experience is a plus
- Excellent interpersonal, organizational, and communication skills
- Excellent analytical and problem solving skills
- High attention to detail and accuracy
- Ability to recognize problems and take corrective measures
- A team player who is open to wearing many hats and willing to jump in when needed
- Diversity and flexibility to support Nventric’s goals in collaboration with different disciplines
- Computer literate including word processing, spreadsheets, database, presentation, graphics
Benefits:
- Health insurance
- Dental insurance
- Vision insurance
- Sick time off
- Employee assistance program
- Employee discount
- Flexible spending account
- Health savings account
- Life insurance
- 401(k)- after 90 days
Job Type: Temporary
Pay: From $26.00 per hour
Expected hours: 40 per week
Ability to Commute:
- Arcadia, CA 91006 (Required)
Work Location: In person
Salary : $26
