Senior Director, Quality Engineering

Reposted 3 Hours Ago
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Cartago, Cartago, CRI
In-Office
Senior level
Healthtech • Pharmaceutical
The Role
Leads quality engineering for medical device new product introduction, lifecycle management, and continuous improvement. Directs quality and process projects, risk mitigation, root cause investigations, complaint evaluations, corrective actions, product and process changes, audits, and standardized global programs. Partners with senior leaders and cross-functional teams, develops quality engineering strategies and metrics, and leads talent development, succession planning, and technical teams while ensuring regulatory compliance.
Summary Generated by Built In

Imagine how your ideas and expertise can change a patient’s life. Our Global Operations & Quality team plays a central part in ensuring our products are delivered to patients with cardiovascular disease. You’ll partner cross-functionally with manufacturing operations and sales teams, delivering thoughtful solutions to complex challenges all while developing your knowledge of the medical device industry. Whether your work includes strategic inventory planning, labeling, warehouse management, material handling, or any of our other supply chain opportunities, you will be making a meaningful contribution to our team and to patients all over the world. 

Leader in Quality Engineering responsible for New product introduction, Lifecycle Management, and product and process continuous improvement in a fast pace manufacturing environment.  

How you'll make an impact:

  • Plan, prioritize, and direct strategic program activities including product, process, and quality projects using engineering methods (e.g., Six Sigma and LEAN methods) to align with applicable compliance standards. Lead in identifying risk, developing complex mitigation strategies, alternative solutions, resolving issues, etc. in collaboration with cross functional groups.
  • Collaborate with leadership to develop operational strategy. Partner with cross-functional groups/resources to achieve tactical execution of business objectives.
  • Provide technical guidance to cross-functional teams on quality engineering activities that integrate into multiple product lines and/or systems with significant complexity including root cause analysis investigations, addressing quality issues, complaint product evaluations, development and implementation of corrective actions, initiation and approval of product/process changes.
  • Identify and lead efforts to optimize quality engineering processes and define and implement core competencies, by assessing business needs to develop, propose and implement solution options.
  • Develop robust talent development and succession planning in alignment with functional growth strategies across the quality organization.
  • Collaborate and align with network and COE teams in driving standardized programs and/or processes.
  • Provide quality engagement to audits including resources support, technical and procedural expertise, presentation of information, and effective resolution of issues.

What you'll need (Required):

Bachelor's Degree in related field with at least 10 years experience in engineering and leadership positions in the medical device industry
Experience in Quality Engineering, Quality Management, and/or Regulatory Compliance within the medical device industry
Demonstrated track record in management of technical and/or engineering disciplines
Proven successful interaction with Regulators and Notified Bodies

Experience influencing  teams in a global environment

What else we look for (Preferred):
• Proven successful project management leadership skills
• Proven expertise in both Microsoft Office Suite and related systems
• Excellent problem-solving, organizational, analytical and critical thinking skills including high discretion/judgment in decision making
• Excellent documentation and communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives
• Expert understanding of engineering procedures while looking beyond existing methodologies and own discipline to define and resolve complex problems
• Expert understanding of related aspects of quality engineering processes and/or systems
• Expert knowledge of domestic and international regulatory requirements 
• Expert knowledge of design of experiments, process capability studies, failure mode and effects analysis, statistical process control, industrial statistical methods and Lean Manufacturing
• Knowledge of financial acumen as it relates to the business as well as quality engineering
• Demonstrated ability to direct teams and provide coaching and feedback, including responsibility for all employee actions including hire/fire authority and partnering with HR on all aspects of employee relations
• Ability to develop and integrate metrics into the projects and operations that clearly demonstrate the value of quality engineering to the business
• Serve as core partner to senior leaders in Business Units, Functional Groups, Regions and IT
• Strict attention to detail
• Ability to interact professionally with all organizational levels and proactively escalate issues to appropriate levels of management in the organization
• Ability to work and excel within a fast paced, dynamic, and constantly changing work environment
• Interacts with senior management, and others concerning matters of significance to the company
• Conduct business and technical briefings for senior and top management and for external representatives
• Regularly interacts with executives and/or major customers; interactions frequently involve special skills, such as negotiating with customers or management or attempting to influence senior level leaders regarding matters of significance to the organization
• Dedicated to quality client service and pro-active and responsive to client needs.
• Develop peer, cross functional and cross business relationships to maximize best practice sharing and team effectiveness.
• Provide leadership and direction to large cross-functional teams to successfully implement global enterprise systems and related solutions
• Develop relationships and leverage them to influence change
• Support and solicit input from team members at all levels within the organization
• Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control

Skills Required

  • Bachelor's degree in a related field
  • At least 10 years of experience in engineering and leadership positions in the medical device industry
  • Experience in Quality Engineering, Quality Management, and/or Regulatory Compliance within the medical device industry
  • Demonstrated track record managing technical and/or engineering disciplines
  • Proven successful interaction with regulators and notified bodies
  • Experience influencing teams in a global environment
  • Project management leadership skills
  • Expertise in Microsoft Office Suite and related systems
  • Problem-solving, organizational, analytical, critical thinking, documentation, communication, negotiation, and relationship management skills
  • Expert understanding of engineering procedures and complex problem resolution
  • Expert understanding of quality engineering processes and systems
  • Expert knowledge of domestic and international regulatory requirements
  • Expert knowledge of design of experiments, process capability studies, FMEA, statistical process control, industrial statistics, and Lean Manufacturing
  • Financial acumen related to business and quality engineering
  • Ability to direct teams and provide coaching, feedback, hiring, termination, and employee-relations support
  • Ability to develop and integrate project and operational metrics
  • Ability to lead large cross-functional teams implementing global enterprise systems and related solutions
  • Ability to work effectively in a fast-paced, dynamic, changing environment

Edwards Lifesciences Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Edwards Lifesciences and has not been reviewed or approved by Edwards Lifesciences.

  • Healthcare Strength Health coverage is considered strong, with multiple plan choices, HSA options, and fertility support, and the company highlights holistic well‑being programs.
  • Retirement Support A company 401(k) match and well‑regarded retirement offerings add clear long‑term value to total compensation.
  • Equity Value & Accessibility An Employee Stock Purchase Plan with a discount and look‑back feature makes equity ownership accessible and enhances the total rewards package.

Edwards Lifesciences Insights

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The Company
HQ: Irvine, CA
13,687 Employees
Year Founded: 1958

What We Do

Edwards Lifesciences (NYSE: EW), is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. We thrive on discovery and expanding the boundaries of medical technology, serving patients in 100+ countries, with the help of our employees in areas including Clinical Affairs, Quality Engineering, Research & Development, Regulatory Affairs, Sales & Marketing, corporate functions and more. Our roots date back to 1958 when Miles Lowell Edwards, a retired engineer with a background in hydraulics and fuel pump operations, set out to build the first artificial heart. Edwards believed the heart could be mechanized and was encouraged by Dr. Albert Starr to focus on developing an artificial heart valve. After just two years, the first Starr-Edwards mitral valve was developed and successfully placed in a patient. This innovation spawned Edwards Laboratories. Miles’ fascination with healing the heart and helping patients with heart disease stemmed from his own experience with rheumatic fever as a teenager and continues to fuel our patient-first culture today. Today, we are as passionate about providing innovative solutions for people fighting cardiovascular disease as we have ever been. It's our Credo. It takes integrity, collaboration, innovation, and focus. We are leaders in the design and manufacture of tissue replacement heart valves and repair products as well as advanced hemodynamic monitoring. We partner with physicians to innovate products designed to help patients live longer, healthier, and more productive lives. Our work is both rewarding and a privilege. The importance of what we do defines our approach. We work together to create an environment where ideas can flourish and we provide our people with the resources, expertise and support to bring those ideas to life. For our legal terms and trademarks, please visit: https://www.edwards.com/legal/legal-terms

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