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Full Time Project Coordinator

2 months ago

Fort Mill, South Carolina, United States Jobot Full time

Job Summary:

A leading medical company is seeking a Quality Assurance Specialist to join their Global Quality and Regulatory Department. As a key member of the team, you will collaborate with cross-functional teams to maintain and improve quality systems and ensure compliance with regulatory requirements.

Key Responsibilities:

  • Work with the Global Quality and Regulatory Department to develop and implement quality systems
  • Collaborate with cross-functional teams to ensure compliance with regulatory requirements
  • Participate in projects to maintain and improve quality systems
  • Conduct audits and inspections to ensure compliance with quality standards
  • Develop and implement corrective action plans to address quality issues

Requirements:

  • 5 years of experience in Quality Assurance, preferably in the medical industry
  • Experience with medical device quality systems (ISO is required)

What We Offer:

  • Medical, Dental, Vision benefits
  • Generous PTO, vacation, sick, and holidays
  • Flexible scheduling to assist with commutes and allow people to handle everyday affairs

Company Overview:

Our company is a leading medical device company with offices in the US, Europe, and Australia. We have been in business for over 20 years and are committed to providing high-quality products and services to our customers.