Quality Manager

JRG Partners

$70K — $95K *
Manufacturing & Automotive
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • BS in Quality Standards or related field, or 2+ years experience managing a quality program
  • Experience in the Medical Device or FDA-regulated industry is essential
  • Proven background in running ISO 9001:2015 standards
  • Hands-on inspection experience of incoming medical products
  • Experience with auditing organizations and presenting audit records
  • Strong verbal and written communication skills
  • Adept in data analysis and statistical methods
  • Excellent interpersonal skills
  • Detail-oriented and diligent
  • Proficiency in Microsoft Office (Excel, Word, PowerPoint)

Responsibilities

  • Implement and execute product inspection and evaluation methods
  • Prepare reports on inspections and receiving processes
  • Report quality standard issues to upper management
  • Supervise staff to uphold quality standards
  • Maintain a Quality Management System in line with industry standards
  • Conduct and manage company training and qualification programs
  • Monitor and communicate on product recalls with upper management and customers
  • Maintain comprehensive product photo library for warehouse

Benefits

  • Opportunity to work in a critical area of quality management in the Medical Device industry
  • Engagement with various department heads to shape quality standards
  • Involvement in maintaining ISO Certification, a prestigious industry standard
  • Access to continuous training and professional development programs
  • Chance to lead audits and interact with certification authorities
Full Job Description
Job Description

We are seeking Quality Manager to assist the various department heads in formulating quality standards and regulations for employees and products. They must analyze data gathered and plan accordingly to improve quality output. They will be accountable for identifying mistakes and quality related processes from purchasing, receiving, storing and shipping, that are crucial to maintaining ISO Certification.

Duties and Responsibilities

The Quality Manager is responsible for implementing and executing inspection and evaluation methods to ensure products adhere closely to company standards
  • Prepare reports by collecting data on inspections or other aspects of the receiving process
  • Reporting to upper management regarding quality standard issues
  • Work according to deadlines while delivering outstanding service within the industry's needs
  • Supervising staff and ensuring qualitative standards are maintained
  • Work with a Quality Management System keeping up to date on current industry standards and ensuring company maintains all standards.
  • Conduct and manage company training and qualification program.
  • Monitor and maintain product recall database. Communicate recalls to upper management and interface with customers on product recalls.
  • Maintain a photo library of all products brought into the warehouse for sale.
  • Present a Quality Management system for multiple audits throughout the year by customers and certification authorities.

Qualifications

BS in Quality Standards or other related field of study or 2 years plus experience in running a quality program.
  • Experience in Medical Device or other FDA-regulated industry a MUST
  • Previous experience running an ISO 9001:2015 International Standards
  • Hands-on experience with the inspection of incoming medical products
  • Confidence and past experience with both auditing organizations and presenting records for audit by outside organizations
  • Excellent verbal and written communication
  • Data analysis and statistical aptitude
  • Excellent interpersonal skills
  • Highly conscientious and diligent
  • Microsoft Office: Excel, Word, PowerPoint

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