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Senior Quality Engineer II

Werfen

Bedford, MAOnsitePosted 12 days ago$150,000 - $180,000/year
Full TimeSenior LevelQuality (QA / QC)Diagnostics
Original posting ↗

Summary

The position is responsible to ensure that activities throughout the product lifecycle are in compliance with procedures, standards and regulations applicable to our products. This position provides project level leadership, independently develops, applies, and implements methods, tools and practices to achieve product quality goals and requirements in the areas of design, development, production, distribution, 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 and production controls.

Job description

Position Summary

The position is responsible to ensure that activities throughout the product lifecycle are in compliance with procedures, standards and regulations applicable to our products. This position provides project level leadership, independently develops, applies, and implements methods, tools and practices to achieve product quality goals and requirements in the areas of design, development, production, distribution, 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 and production controls.

Key Accountabilities

  • Participates in the generation and review of quality documents throughout the product lifecycle
  • Advises and directs teams regarding compliance to procedures, standards and regulations
  • Ensures product quality meets requirements and documentation is complete prior to approval
  • Participates on core teams supporting new product development or design changes
  • Defends relevant quality topics in audits and corrective actions to improve and maintain compliance of the QMS
  • Interprets regulations and procedures to ensure documents are sound and defensible to auditors and regulatory bodies
  • On projects of significant scope, leads successful implementation of Design Control and Product Realization requirements for design, production and distribution of IL products
  • On new product development and or product performance investigations, provides guidance on most appropriate tools and techniques available
  • Provides input on product requirements, acceptance criteria, traceability, process monitoring, product evaluation, failure investigation and complaint analysis
  • Ensures application of sound statistical methods and quality tools in the evaluation and documentation of results related to design control, purchased part qualifications, V&V, risk analysis, production transfer, production, distribution and marketing of IL products
  • Provides guidance on compliance of software to procedures and standards including cyber security and privacy requirements
  • Works with manufacturing, R&D, Service, Distribution, Sales & Marketing, and others outside the company (as needed) to recommend or prepare corrective/preventive actions (CAPA)
  • Reviews and approves change orders for product performance, process changes, labeling and marketing communications as required
  • May manage and supervise the work of others
  • Leads cross-functional projects on technical and quality issues
  • Other duties as assigned

Secondary Functions

  • Identifies compliance gaps and takes appropriate corrective actions as needed
  • Defends documents and procedures internal and external audits
  • Leads quality system improvement projects as required

Skills & 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 IL 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

Minimum Knowledge & Experience

  • Bachelor's degree or equivalent in engineering or science
  • A minimum of 10 years of experience in medical devices, pharmaceuticals, diagnostic industry, or clinical laboratory or 7 years of experience with an advanced degree
  • Duties necessitate broad and thorough knowledge of engineering and science theory and principles, including R&D, quality control, manufacturing and design engineering
  • Understanding of the application of technical principles and engineering problem solving to resolve complex issues
  • ASQ Quality Engineering Certification - Desirable
  • LEAN/Six Sigma Certification - Desirable
  • Language: English
  • Travel Requirements: Approximately 10% of time

Requirements

  • Bachelor's degree or equivalent in engineering or science
  • A minimum of 10 years of experience in medical devices, pharmaceuticals, diagnostic industry, or clinical laboratory or 7 years of experience with an advanced degree
  • Working knowledge of domestic and international quality/regulatory standards related to our products
  • Knowledge of quality management techniques (Lean, Six Sigma) and statistical techniques
  • Working knowledge of IL products, technology and manufacturing processes
  • Demonstrated understanding of risk based approach to processes and decisions
  • ASQ Quality Engineering Certification - Desirable
  • LEAN/Six Sigma Certification - Desirable
  • Language: English
  • Travel Requirements: Approximately 10% of time

Benefits

  • Medical, Dental & Vision
  • 401(k) Matching
  • Paid Vacation
  • Sick Leave
  • Performance-Based Bonus

Company overview

Werfen is a global leader in specialized diagnostics, founded in 1966 in Barcelona, Spain as a family-owned innovative company. The organization has established itself as a worldwide authority in five key clinical areas: Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant diagnostics. With headquarters in Barcelona and technology centers strategically located in the United States and Europe, Werfen operates directly in 30 countries and serves more than 100 territories through distributors. The company achieved remarkable financial performance with worldwide sales exceeding €2.2 billion in 2024, supported by a workforce of over 7,000 employees globally. Werfen's comprehensive portfolio includes advanced diagnostic systems, reagents, laboratory automation solutions, and point-of-care testing platforms that enable healthcare providers to deliver precise and timely patient care. Their innovative technologies span from blood gas analyzers with hemolysis detection capabilities to automated immunoassay systems and specialized diagnostic assays. As a vertically integrated diagnostics company, Werfen maintains complete control over research, development, manufacturing, and distribution, ensuring quality and reliability across their product lines while continuously advancing diagnostic science to address critical healthcare challenges worldwide.

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