Director of Quality

Rush, NY

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Description

Remedy Intelligent Staffing is currently sourcing for a Director of Quality for a leading global manufacturer in the healthcare market.

Our client creates high quality, innovative medical products, many of which are manufactured in the United States. With eleven manufacturing/ distribution facilities around the world, our client services the global healthcare community in an efficient and timely manner.

Position Overview:

The Director of Quality will provide leadership for Quality Assurance and Quality Control functions that support products and operational processes. The Director of Quality is responsible for maintaining compliance in all quality-related activities and systems. This individual will facilitate all continuous improvement efforts and objectives, lead organizational efforts to collaborate, in effort to maintain quality system compliance. The Director of Quality will serve as an integral factor in the development, implementation, and management of corporate Quality objectives.

Essential Functions:

  • Provide leadership and vision for quality objectives, both internally and externally
  • Develop members of the Quality Assurance team, mentor colleagues within the organization, and foster the growth of the QA organization
  • Facilitate clear lines of communication between Quality Assurance and other departments internally
  • Develop long and short-term projections for quality programs, objectives, initiatives, and cost budgeting
  • Be a leading member for compliance with FDA and ISO regulations
  • Partake in FDA and ISO Audits
  • Promote teamwork across multiple departments, including operations, research and development, regulatory, sales, and marketing
  • Facilitate an atmosphere of prompt corrective action when quality issues arise
  • Collaborate with Director of Global Quality System Compliance, and other leadership to ensure adherence to quality Systems
  • Manage cross-functional efforts, organize and schedule reviews, and participate in leadership meetings

Requirements:

  • BA or BS Degree in a technical discipline
  • 7-10 years’ in the medical device industry preferred
  • Must be knowledgeable and able to operate under FDA, ISO, cGMP, and cGLP regulations
  • Must possess strong leadership abilities, interpersonal skills, and experience effectively managing multi-discipline teams
  • Strong written and oral skills, strong problem solving abilities, and attention to detail

Benefits include company-contributed medical and dental coverage, 401K plan with company match, 15 holidays and PTO, life insurance, and more.

Job Requirements

Remedy Intelligent Staffing is currently sourcing for a Director of Quality for a leading global manufacturer in the healthcare market.

Our client creates high quality, innovative medical products, many of which are manufactured in the United States. With eleven manufacturing/ distribution facilities around the world, our client services the global healthcare community in an efficient and timely manner.

Position Overview:

The Director of Quality will provide leadership for Quality Assurance and Quality Control functions that support products and operational processes. The Director of Quality is responsible for maintaining compliance in all quality-related activities and systems. This individual will facilitate all continuous improvement efforts and objectives, lead organizational efforts to collaborate, in effort to maintain quality system compliance. The Director of Quality will serve as an integral factor in the development, implementation, and management of corporate Quality objectives.

Essential Functions:

  • Provide leadership and vision for quality objectives, both internally and externally
  • Develop members of the Quality Assurance team, mentor colleagues within the organization, and foster the growth of the QA organization
  • Facilitate clear lines of communication between Quality Assurance and other departments internally
  • Develop long and short-term projections for quality programs, objectives, initiatives, and cost budgeting
  • Be a leading member for compliance with FDA and ISO regulations
  • Partake in FDA and ISO Audits
  • Promote teamwork across multiple departments, including operations, research and development, regulatory, sales, and marketing
  • Facilitate an atmosphere of prompt corrective action when quality issues arise
  • Collaborate with Director of Global Quality System Compliance, and other leadership to ensure adherence to quality Systems
  • Manage cross-functional efforts, organize and schedule reviews, and participate in leadership meetings

Requirements:

  • BA or BS Degree in a technical discipline
  • 7-10 years’ in the medical device industry preferred
  • Must be knowledgeable and able to operate under FDA, ISO, cGMP, and cGLP regulations
  • Must possess strong leadership abilities, interpersonal skills, and experience effectively managing multi-discipline teams
  • Strong written and oral skills, strong problem solving abilities, and attention to detail

Benefits include company-contributed medical and dental coverage, 401K plan with company match, 15 holidays and PTO, life insurance, and more.

Apply Now