Quality Manager

Reposted 13 Days Ago
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Oak Ridge, TN, USA
In-Office
Entry level
Hardware • Healthtech • Defense • Manufacturing
The Role
Oversee the company’s quality, safety, and environmental management systems. Responsibilities include conducting audits, managing nonconformances and corrective actions, maintaining inspection and calibration programs, reviewing statistical data, preparing qualification reports and regulatory submissions, coordinating safety training, and ensuring compliance with ISO standards and applicable regulations.
Summary Generated by Built In

Join Mirion in our mission to harness our unrivaled knowledge of ionizing radiation for the greater good of humanity.

Dosimetry Services, a Mirion Medical Company, offers products and services that better the human condition by removing the worry of radiation from the daily routines of those who are occupationally exposed. Delivering Better Tools for Safer Workspaces.

The Quality Manager will oversee all compliance related activities applicable to the organization’s Quality Management system and Safety Management system. This will consist of performing customer and compliance audits, evaluating Conditions Adverse to Quality events, and ensuring that the organization complies to local, State, and government regulations regarding Safety and environmental matters. They will act as the liaison for all regulatory agencies.

JOB RESPONSIBILITIES, DUTIES & CORE FUNCTIONS:

  • Establish, formulate, and audit the QA, EMS, and OSHAS procedures necessary for the company to meet ISO standards and other standards that may become a requirement.
  • Oversee and liaison with Technical team, Procurement, and Production for programs including but not limited to: Condition Adverse to Quality program, Training program, Internal Audit program, and Software quality assurance program.
  • Overseeing of the maintenance and calibration of all inspection equipment, random inspection of in-process and finished assemblies, disposition of all non-conforming materials, & Incoming inspections.
  • Oversee Internal Audit Program in compliance with applicable Regulatory requirements.
  • Assure appropriate data is efficiently obtained and review, analyze and correlate test data using statistical techniques.
  • Author Lot Qualification Reports with sufficient detail and objective evidence to demonstrate conformance.
  • Investigate and participate in root cause analysis and retest of any failures or discrepancies when required.
  • Ensure company corrective actions are assigned, completed, verified, and closed in a timely manner.
  • Review and stay current with applicable safety and environmental regulations.
  • Conduct safety awareness training at company level.
  • Work with Operations to establish and track safety metrics.
  • Prepare and submit required Regulatory Submissions, including annual compliance reports.
  • Report to Top Management on the quality of the management systems.  
  • Other duties as assigned.

REQUIRED EDUCATION, SKILLS, QUALIFICATIONS, & EXPERIENCE

Education

  • Bachelor’s Degree in a technical discipline or equivalent and relevant work experience.
  • Prior experience in Quality, Health & Safety, or Manufacturing Management
  • Prior experience with Document Control in a regulated industry

PREFERRED SKILLS

  • Prior experience in Quality, Health & Safety, or Manufacturing fields
  • Prior experience working in a radiological test environment
  • Sound knowledge of regulatory requirements including ISO 17025 and/or ISO 9001
  • Prior audit experience following ISO 19011
  • Experience with generating and presenting quantitative reports
  • Excellent written communication skills and proficient in the use of Excel and/or other tools for the reporting and statistical analysis of data
  • Working knowledge of CAD principles
  • Ability to read and interpret Safety Data Sheets
  • Must be able to work with minimal direct supervision
  • Detail-oriented, analytical, and methodical a thinker

PHYSICAL REQUIREMENTS & WORK ENVIRONMENT

Physical Requirements

  • May be required to lift and move up to 50 pounds
  • May be required to sit and stand while performing reader daily functions
  • May be required to bend and reach while performing reader maintenance
  • May occasionally work with hazardous materials including chemicals and radioactive materials
  • While performing the duties of this job, the employee is sitting at a desk in a cubicle setting or standing to perform reader task

Work Environment

  • Climate-controlled facility with medium noise level

Skills Required

  • Bachelor’s degree in a technical discipline or equivalent relevant work experience
  • Prior experience in Quality, Health and Safety, or Manufacturing Management
  • Prior experience with document control in a regulated industry
  • Prior experience in Quality, Health and Safety, or Manufacturing fields
  • Prior experience working in a radiological test environment
  • Knowledge of ISO 17025 and/or ISO 9001 regulatory requirements
  • Prior audit experience following ISO 19011
  • Experience generating and presenting quantitative reports
  • Proficiency with Excel and/or other tools for reporting and statistical data analysis
  • Working knowledge of CAD principles
  • Ability to read and interpret Safety Data Sheets
  • Ability to work with minimal direct supervision
  • Detail-oriented, analytical, and methodical approach
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The Company
HQ: Atlanta, GA
3,281 Employees
Year Founded: 2005

What We Do

Mirion is a global provider of radiation safety and science technologies, partnering with customers across science, industry, and medicine. The company develops detection, measurement, analysis, and monitoring solutions for nuclear, defense, medical, and research end markets. Its medical group supports healthcare from diagnosis through treatment, while its mission is to harness ionizing radiation knowledge to protect people and advance critical innovation.

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