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Quality Assurance Specialist

Job in Indianapolis, Marion County, Indiana, 46201, USA
Listing for: Cynet Systems
Full Time position
Listed on 2026-08-29
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Data Analyst
Salary/Wage Range or Industry Benchmark: 31 - 36 USD Hourly USD 31.00 36.00 HOUR
Job Description & How to Apply Below
Position: Quality Assurance Specialist I

Quality Assurance Manager

Pay Range: $31.00hr - $36.00hr

Requirement/Must Have:

  • Two or more years of experience in Quality or a related function.
  • Bachelor’s / Master’s degree in Life Science, Data Science, or a related subject or equivalent experience.
  • Professional experience in a similar role within the medical device sector.
  • Knowledge of deviation and resolution management.
  • Expertise in quality systems, standards and regulations, specifically production and/or supplier development processes and standards such as ISO 13485 and ISO 27001.
  • Strong analytical skills with a focus on essential facts.
  • Strong verbal and written communication skills.
  • Cultural awareness and experience interacting with global internal and external partners and suppliers.
  • Leadership mindset with the ability to lead others within an agile organization.
  • Willingness and flexibility to collaborate cross-continentally in a global team across different time zones (may require early working hours to ensure close collaboration with colleagues in the XX Union).
  • Decisive and able to initiate and complete daily activities and proactively find solutions independently with limited guidance.

Responsibilities:

  • Manage the ETE IVDR/MDR product verification process for products within distributed products portfolio, including determining requirements and controls for those products and completing objective evidence of supplier evaluation and approval.
  • Manage SCARs (Supplier Corrective Action Requests) and successfully complete them, as well as address other supplier gaps in a timely manner by tracking robust corrective action plans.
  • Complete onboarding activities for suppliers.
  • Monitor supplier performance.
  • Plan and follow up on supplier audits and ensure resulting supplier actions are sufficient to resolve quality issues and are completed in a timely fashion.
  • Identify and escalate issues as they arise and provide adequate solutions.

Skills:

  • Quality Assurance.
  • Medical Device Sector.
  • ISO 13485.
  • ISO 27001.
  • Supplier Quality Management.
  • SCARs.
  • IVDR/MDR.
  • Supplier Audits.
  • Analytical Skills.

Qualification And

Education:

  • Bachelor’s or Master’s degree in Life Science, Data Science, or a related field.
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