Instrumentation Laboratory Company

Senior Software Quality Engineer

Healthcare
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in engineering or science or equivalent experience
  • Minimum of 8 years in medical devices, pharmaceuticals, diagnostics, or clinical lab work
  • Strong understanding of quality/regulatory standards
  • Experience with quality management and statistical techniques
  • Judgment regarding regulatory requirements and risk management application

Responsibilities

  • Generate quality documents throughout the product lifecycle
  • Advise teams on compliance with standards and regulations
  • Ensure product quality and completeness of documentation before approval
  • Support new product development and design changes
  • Review and approve quality documents
  • Assist with audits and corrective actions
  • Identify compliance gaps and implement corrective measures

Benefits

  • Medical, dental, and vision insurance
  • 401(k) plan with employer match
  • Paid vacation and sick leave
  • Participation in commission plan for sales roles
  • Performance-based bonus eligibility for management and select roles
Full Job Description
Introduction

Overview

Position Summary:

The Senior Software Quality Engineer position is responsible to ensure that activities throughout the product lifecycle are in compliance with procedures, standards and regulations applicable to our products. In this capacity the Sr SWQE independently develops, applies and implements methods, tools and practices while working with project teams to achieve product quality goals and requirements in the areas of design, development, cybersecurity, verification and validation, maintenance and service. This is a technically focused role requiring advanced skills in analyzing information, reviewing technical reports, promoting process improvement, requirements development, risk management, product development, verification and validation, and cybersecurity.

Responsibilities

Key Accountabilities:
  • Participates in the generation of quality documents throughout the product lifecycle.
  • Advises and directs teams regarding compliance to procedures, standards and regulations. Implement changes to procedures in alignment with evolving regulations.
  • Ensures product quality meets requirements and documentation is complete prior to approval.
  • Participates on core teams supporting new product development or design changes.
  • Reviews and approves quality documents throughout the product lifecycle
  • Supports audits and corrective actions to improve and maintain compliance of the QMS
  • Identifies compliance gaps and takes appropriate corrective actions as needed
  • Participates in and may lead quality system improvement projects as required.
  • Performs other duties and responsibilities as assigned. Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.

Budget Managed (if applicable):
  • N/A

Internal Networking/Key Relationships:

To be determined based on department needs, to include interactions such as:
  • Works closely with other functions to generate compliant documents by interpreting and explaining quality procedures, applicable standards, regulations and best practices.
  • Able to effectively communicate quality requirements to a broad population of constituents.
  • Ability to negotiate and influence others in establishing direction toward improved quality and enhanced compliance.

Skills & Capabilities:

The ideal candidate for this position will exhibit the following skills and capabilities:
  • Working knowledge of domestic and international quality/regulatory standards related to our products
  • Knowledge of quality management techniques (Lean, Six Sigma) and statistical techniques required to measure and confirm significant changes.
  • Working knowledge of products, technology and manufacturing processes including impact on customers and patient requirements.

Demonstrates judgement commensurate with experience regarding application of regulatory requirements to data review, reports, design changes, risk management, etc. to ensure compliance and achieving business objectives. Demonstrated understanding of risk-based approach to processes and decisions.

Qualifications

Minimum Knowledge & Experience Required for the Position:

Education: Bachelor's degree or equivalent in engineering or science.
Experience: A minimum of 8 years of experience in medical devices, pharmaceuticals, diagnostic industry, or clinical laboratory of 5 years of experience.
Management has the discretion of substituting relevant work experience for a degree and/or making exceptions to the years of experience requirement.

International Mobility Required:
  • No

Travel Requirements:
  • Approximately 10%


The annual base salary range for this role is currently $130K - $160K. Individual employee compensation will ultimately depend on factors including education, relevant experience, skillset, knowledge, and particular business needs.

This role is eligible for medical, dental, and vision insurance, 401k plan retirement benefits with an employer match, as well as paid vacation and sick leave. Our sales roles are eligible for participation in a commission plan and our management, and select professional roles, are eligible for a performance-based bonus.

Closing

If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV.

About Instrumentation Laboratory Company

Instrumentation Laboratory Company (IL) is a global leader in the development, manufacturing and distribution of diagnostic solutions for Acute Care Diagnostics, with a focus on Critical Care and Hemostasis testing. Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. IL develops, manufactures and distributes diagnostic solutions including: critical care systems, hemostasis systems and information management systems. IL's products are used in hospitals around the world, including large hospital systems, independent hospitals and clinics, and reference laboratories. IL is headquartered in Bedford, Massachusetts, and has operations in Europe, the Middle East, Africa, Asia-Pacific, and Latin America.
Learn more about Instrumentation Laboratory Company
Size
1,000 employees
Industry
Net Income
$50 million
5 Year Trend
+5%
Revenue
$500 million

Similar Jobs

More Jobs at Instrumentation Laboratory Company

More Healthcare Jobs

Find similar Senior Software Quality Engineer jobs: