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Regulatory Affairs and Quality Assurance Associate (Medical Device)

Jobs via Dice
Pittsburgh, PA Full Time
POSTED ON 4/13/2026
AVAILABLE BEFORE 5/13/2026
Dice is the leading career destination for tech experts at every stage of their careers. Our client, INNOVIT USA INC, is seeking the following. Apply via Dice today!

About The Job

Experience/Knowledge/Technical Skills Required:

  • Around 2 to 5 years of experience in implementation in the QA domain preferably with some experience in working in the Medical Devices industry
  • Internal/Lead Auditor of Quality Management Systems
  • Knowledge and application skills of QC/Problem solving tools
  • Good computer skills
  • Knowledge of relevant regulatory/CE requirements for medical devices will be preferred 6. Analytical and structured working style, attention to details
  • Ability to work as part of a team
  • Good verbal and written communication skills

Roles & Responsibilities

  • Implementation and continuous improvement of the Medical Device Quality
  • Management Systems and associated CE requirements in order to meet customer
  • and regulatory requirements
  • Preparation, implementation, and Maintenance of Manual, policies, work instructions as per ISO 13485 5. Preparation, implementation, and Maintenance of Technical documentation (MDR) wrt applicable requirements
  • Review and formal approval of technical reports.
  • Facilitate internal/external audits and evaluate audit findings and implement
  • appropriate corrective actions
  • Investigate customer complaints and non-conformance issues
  • Analyse data to identify areas for improvement in the quality system
  • Identify training needs and organize training interventions to meet quality standards
  • Monitor risk management activities
  • Responsible for document management systems
  • Managing the Inventory & Batch Verifications
  • Management Representative: responsibilities shall be -
  • ensuring that processes needed for the quality management system are documented;
  • reporting to top management on the effectiveness of the quality management system and any need for improvement;
  • ensuring the promotion of awareness of applicable regulatory requirements and quality management system requirements throughout the organization.

Salary.com Estimation for Regulatory Affairs and Quality Assurance Associate (Medical Device) in Pittsburgh, PA
$84,427 to $104,572
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