Quality Systems Engineer II

CryoLife

$80K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a technical/scientific field or equivalent work experience
  • 3+ years in quality engineering, quality assurance, or a similar role
  • Preferred certifications include ASQ CQA/CQE/LSS or AATB CTBS
  • Experience with electronic quality management systems and QA software tools
  • Strong analytical and problem-solving abilities
  • Excellent verbal and written communication skills
  • Knowledge of Good Manufacturing Practices, Tissue Banking Regulations, and ISO Standards

Responsibilities

  • Oversee implementation and maintenance of the Quality Management System
  • Support corporate quality objectives within budget
  • Coordinate corrective and preventive actions using root cause analysis
  • Perform verification on CAPA and nonconformances
  • Conduct gap analyses to new Quality System standards
  • Maintain and update Quality System Procedures
  • Participate in internal and external Quality System audits
  • Report data on Key Performance Indicators (KPIs)
  • Drive continuous improvement initiatives
  • Engage in ongoing training and development, including lead auditor training

Benefits

  • Training and development opportunities
  • Support for professional certification
  • Engagement in continuous improvement activities
  • Involvement in a collaborative workplace culture
  • Access to quality management resources and tools
Full Job Description
Position Objective:

Responsible for operating the Quality Management System (QMS). To assist in providing assurance the Company operates in compliance with all required regulations and standards as determined by both internal and external assessments. Support internal audits and help manage external assessments. Provide training where necessary. Assure the Corrective and Preventive Action Program (CAPA) and Audit Program requirements comply with all applicable requirements and keep management advised of the status of these programs. To assist with management review, nonconformance oversight, quality planning, and change control. To administer the electronic quality management system and perform gap analysis as identified.

Responsibilities:
  • Oversee effective implementation and maintenance of the Quality Management System throughout the company
  • Support corporate quality objectives and achieve those goals within budget.
  • Coordinate corrective and preventive actions, provide solutions, and improvements using root cause analysis tools to resolve issues
  • Perform effectiveness verification on CAPA and nonconformances
  • Conduct gap analyses to new or revised Quality System standards and regulations
  • Maintain Quality System Procedures and ensure contents are appropriate for business
  • Participate in external/internal Quality System audits including supporting the backroom.
  • Effectively report data to management on Key Performance Indicators (KPIs)
  • Contribute to continuous improvement activities
  • Undertake continuous training and development, including lead auditor training
  • Monitor nonconformances and CAPAs to ensure timely completion
  • Efficiently drive on time closure of Quality System audit findings
  • Perform root cause analysis and investigation support to resolve problems
  • Manage oversight of the corporate change control process
  • Provide management with training support of QSE I
  • Assist with the development, maintenance, and support for the eQMS software systems
  • Support Tissue Recovery Partner audit assessments
  • Assist with QMS management review
  • Monitor Quality plans and GAPs for on time reporting of activities and assist where needed

Qualifications:
  • Bachelor's degree in a technical / scientific related field, or an equivalent field of study, or the equivalent years' work experience.
  • 3+ years of experience in quality engineering, quality assurance, or a similar role.
  • ASQ CQA/CQE/LSS and/or AATB CTBS or other auditing certification preferred.
  • Experience with electronic quality management systems and using QA software tools.
  • Strong analytical and problem-solving skills.
  • Excellent verbal and written communication skills, including business writing.
  • Working knowledge of current Good Manufacturing Practices, Good Tissue Practices, Tissue Banking Regulations, Quality System Regulations, and ISO Standards.

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