Edwards Lifesciences Corp

Sr. Analyst, Quality Systems

Edwards Lifesciences Corp$92K — $130K *
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in related field and 5 years of experience in quality or manufacturing in the medical device industry or equivalent experience.
  • Proven expertise in MS Office Suite.
  • Strong project management skills and familiarity with related software tools.
  • Excellent written and verbal communication skills, notably in negotiation and relationship management.
  • In-depth knowledge of quality system regulations (FDA and ISO13485) relevant to medical devices.
  • Detail-oriented with a commitment to producing high-quality work.
  • Experience affecting change and influencing stakeholders across diverse teams.

Responsibilities

  • Support Corporate Quality initiatives by documenting business requirements and workflows.
  • Partner with various organizational levels to drive results and proactively resolve issues.
  • Lead medium to large scale projects, evaluating multiple factors influencing outcomes.
  • Drive improvements in current practices through collaboration with functional areas.
  • Present updates and escalate issues to senior management, advocating for process simplification and standardization.
  • Interact effectively with IT and compliance, leveraging both business and technical insights.
  • Perform incidental duties as assigned by Leadership.

Benefits

  • Competitive salary and performance-based incentives.
  • Comprehensive benefits programs addressing diverse employee needs.
  • Opportunities for professional development and career growth.
Full Job Description
This role supports all Edwards business units, regions and site through the review, analysis, and evaluation of business needs to create solutions that support overall business strategies. The Senior Quality System Analyst is responsible for effectively partnering with subject matter experts, process owners and functional leaders across the organization in helping to document business requirements, defining scope and objectives that drive process development and implementation while promoting a collaborative atmosphere of quality awareness and continuous improvement. Interact and present to senior management through the escalation process to drive for simplification and standardization across the organization. Functions as an integrator between the business users, IT and corporate compliance with both business and technical expertise.

How you will make an impact:
• Support Corporate Quality strategic initiatives by working with business representatives to understand, and document the business requirements, processes and workflows developing both written and visual depictions of requirements and process flows. Partner effectively with all levels of the organization to drive results, proactively identify and resolve problems, manage conflicts and escalate as required. Work with the Corporate Quality PMO to ensure solutions are successfully developed, deployed and sustained in line with overall Corporate Quality objectives.
• Lead medium to large scale projects where analysis of situations requires an in-depth evaluation of multiple factors and/or requires an in-depth knowledge of organizational objectives in conjunction with Quality / Regulatory compliance requirements. Drive to resolve these issues completely and with speed by leveraging your network of key contacts outside your own area of expertise. You will suggest and drive improvement of current practices and work with the appropriate functions to implement changes or participate in their implementation.
• Other incidental duties assigned by Leadership

What you'll need (Required):
• Bachelor's Degree in related field, 5 years' experience quality and/or manufacturing environment in the medical device industry or equivalent work experience based on Edwards criteria

What else we look for (Preferred):
• Proven expertise in MS Office Suite
• Good project management skills and related software tools preferred
• Excellent written and verbal communication skills including negotiating and relationship management skills
• Strong problem-solving and critical thinking skills
• Full knowledge and understanding of Edwards policies, procedures, and guidelines relevant to quality systems
• Full knowledge of medical or pharmaceutical regulations as relating to documentation
• Full understanding of medical devices regulations (e.g., FDA (21 CFR Part 820) and ISO13485)
• Strict attention to detail producing high quality work
• Ability to interact professionally with all organizational levels. Strong ability to manage and work with different cultures and nationalities, experience working in complex global environment
• Ability to manage competing priorities in a fast paced environment, show initiative and be flexible
• Working experience influencing others to action who are not direct reports
• Work is performed independently on complex projects and reviewed for accuracy and soundness
• Applies sound judgment when making decisions and communicating with peers and management
• Ability to adapt to new technologies and rapidly changing environment
• 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

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.

For California, the base pay range for this position is $92,000 - $130,000 (highly experienced). The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.

About Edwards Lifesciences Corp

Edwards Lifesciences is an American medical technology company headquartered in Irvine, California, specializing in artificial heart valves and hemodynamic monitoring. It developed the SAPIEN transcatheter aortic heart valve made of cow tissue within a balloon-expandable, cobalt-chromium frame, deployed via catheter. The company has manufacturing facilities at the Irvine headquarters, as well as in Draper, Utah; Costa Rica; the Dominican Republic; Puerto Rico; and Singapore; and is building a new facility due to be completed in 2021 in Limerick, Ireland.
Learn more about Edwards Lifesciences Corp
Size
15,700 employees
Market Cap
$45.6 billion
Industry
Net Income
$823.4 million
Founded
1958
5 Year Trend
+12%
Revenue
$4.3 billion
NASDAQ

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