Senior Quality Systems Engineer

TransMedics, Inc.; Andover (MA); On-site; USD 101,000 - 203,000; Full time

Job summary

An established industry player is seeking a Senior Quality Systems Engineer to enhance their Quality team. This role focuses on Quality Systems, CAPA, and Internal Audits, ensuring compliance and driving process improvements. The ideal candidate will bring a strong background in medical devices, showcasing their expertise in managing quality-related activities within a dynamic environment. If you are results-driven and passionate about quality assurance, this opportunity offers a chance to make a significant impact in a fast-paced setting.

Qualifications

• 5-7 years of experience in medical device industry.
• Knowledge of Quality System Standards and regulations.

Responsibilities

• Manage QMS processes for compliance with CAPA and audits.
• Support CAPA Owners with quality-related principles.
• Develop Quality Metrics and coordinate data collection.

Skills

Quality Management Systems (QMS)

CAPA

Internal Audit

Problem Solving

Root Cause Analysis

ISO 13485

21 CFR Part 820

FMEA

Microsoft Office

Education

Bachelor’s Degree in Engineering

Biomedical Science

Job description

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Position Summary

We are seeking a dynamic, analytical thinking individual to join our Quality team, focusing on Quality Systems, CAPA, Internal Audit, metric reporting and process improvement initiatives. The ideal candidate will possess a strong background in medical devices or IVD, with a proven track record in managing quality-related activities in a fast-paced dynamic environment. QMS experience is essential.

Job Description

Senior Quality Systems Engineer

Position Summary

We are seeking a dynamic, analytical thinking individual to join our Quality team, focusing on Quality Systems, CAPA, Internal Audit, metric reporting and process improvement initiatives. The ideal candidate will possess a strong background in medical devices or IVD, with a proven track record in managing quality-related activities in a fast-paced dynamic environment. QMS experience is essential.

Responsibilities

This position is responsible for, but not limited to, the following:

• Supports the overall QMS processes for the organization. Responsible for activities required to ensure compliance of Quality Management Systems (QMS), specifically regarding CAPA and internal/external audits. Additional responsibilities include supporting other QMS functions such as NCMRs, Supplier Controls, Management Review, Risk Review, etc.
• Execution and coordination of activities associated with CAPA program, including administration and record management, providing quality input to investigations, reporting, as well as metrics and trending
• Support CAPA Owners in quality-related technical principles, including but not limited to Problem Solving tools and techniques (Root Cause Analysis, DOE, FMEA, etc.)
• Manages the Internal Audit program, including scheduling audits, ensuring timely response to findings, as well as metrics and trending
• Support external audits and inspections by providing subject matter expertise
• Development of Quality Metrics, and coordination of quality data collection and analyses for use in monthly metrics meetings and Management Reviews
• Provide quality assurance support cross-functionally across the organization
• Lead/participate in Risk Management and FMEA initiatives
• Develop, implement, and manage Quality Control/Quality System process improvements.
• Identify opportunities for improvement within the Quality System to ensure compliance and efficiency. Correct or improve gaps/opportunities in an independent fashion by writing and releasing new or revised Quality System documentation
• Understand how and when to escalate quality issues to leadership team within the organization, presenting data and information necessary to draw conclusions and take action
• Provide training and support to employees on quality processes and procedures
• Support work on quality plans, quality processes and special projects, as required
• Perform other TransMedics tasks and duties as assigned/required
  
  

Management Responsibilities

• This position will not have management responsibilities
  
  

PHYSICAL ATTRIBUTES

• Must be able to lift 50lbs
  
  

Minimum Qualifications

• Bachelor’s Degree in Engineering, Biomedical Science, or other technical discipline preferred, with 5-7 years of relevant experience in medical device industry, including responsibility for Product Quality and/or Quality Systems
• A working knowledge of Quality System Standards and regulations, including 21 CFR Part 820, ISO 13485, EU MDR
• Ability to multi-task, handling multiple projects and changing priorities
• Experience in the creation and documentation of procedures and processes
• Must be results-driven and exhibit a sense of urgency
• Proficiency with Microsoft Office - Word, Excel, PowerPoint and Access experience required
  
  

Preferred Qualifications

• Experience participating in internal and external audits, preferably serving as qualified internal auditor
• Ability to communicate ideas and information clearly, effectively, and frequently (both oral and written)
• Ability to exercise independent judgment in methods, techniques, and evaluation criteria for obtaining results
• Ability to act independently to determine methods and procedures
• Problem-solving skills and the ability to resolve issues as they arise
• Strong interpersonal skills, with the ability to assimilate with various cross-functional teams
  
  

TransMedics is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, national origin, marital status, age, disability or protected veteran status, or any other characteristic protected by law. We are committed to creating an inclusive environment for all employees.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Medical Equipment Manufacturing

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