Technical Writer

USA - California – Irvine

Full time

Req-48933

Many structural heart patients suffer from heart failure with limited options. Our Implantable Heart Failure Management (IHFM) team, part of the AI, Product and Platforms organization, is at the forefront of addressing these unmet patient needs through pioneering technology that enables early, targeted therapeutic intervention. Our innovative solutions are not just transforming patient care but also creating a unique and exciting environment for our team members. It is our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.

At Edwards Lifesciences, the IHFM AI, Product and Platforms organization designs and builds the software and data products that clinicians and patients depend on. As a Technical Writer, you own well-scoped controlled documentation that keeps our regulated software traceable and audit ready. You produce and maintain design control artifacts and user-facing documentation with limited guidance, partnering with engineering, quality, and product.

Based in Irvine, CA, you'll join a high-impact medtech innovation hub in the heart of Orange County, collaborating in person with cross-functional teams to shape patient-focused technology.

How You’ll Make an Impact

• Create and maintain moderately complex Good Manufacturing Practices (GMP) protocols, reports, technical summaries, and test procedures.

• Develop well-scoped controlled documentation that supports regulated software traceability and audit readiness.

• Maintain documentation in a standard format and follow established guidelines for content quality, organization, and consistency.

• Partner with production employees, technicians, engineers, project teams, regulatory partners, and management to understand product, component, or device changes.

• Review documents for style, clarity, grammar, punctuation, and overall usability.

• Identify and resolve inconsistencies in content, structure, or document development, and work with authors to recommend appropriate updates.

• Respond to requests for clarification or explanation of reference materials and technical documentation.

• Support additional documentation-related needs as assigned by leadership.

What you'll need (Required):

• Bachelor’s degree in a related field and 3 years of technical writing experience, or equivalent work experience based on Edwards criteria.

• This is an onsite role based in Irvine, CA. Relocation assistance is not provided, and candidates must reside within a 50-mile radius of Irvine to be considered.

What else we look for (Preferred):

• Biotechnology, medical device, or regulated industry experience, or equivalent work experience based on Edwards criteria.

• Experience creating or maintaining documentation types such as procedures, routers, process sheets, technical summaries, protocols, and test reports.

• Solid understanding of policies, procedures, and guidelines relevant to technical documentation development.

• Strong editing, proofreading, and technical writing skills, with careful attention to style, clarity, grammar, and punctuation.

• Proficiency with Microsoft Office Suite, including Word, Excel, PowerPoint, and Publisher; Adobe and Photoshop experience preferred.

• Good written and verbal communication skills in English, with strong interpersonal skills.

• Good problem-solving, critical thinking, organization, and prioritization skills in a fast-paced environment.

• Ability to work independently on more complex projects or lines of work, with work reviewed for accuracy and soundness.

• Ability to collaborate across interdepartmental teams, build productive internal and external working relationships, and represent the organization on specific projects.

• Strict attention to detail and commitment to following all company rules and requirements, including Environmental Health & Safety expectations and applicable protocols.

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 (CA), the base pay range for this position is $68,000 to $96,000 (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.

Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. Through breakthrough technologies, world-class evidence and partnerships with clinicians and healthcare stakeholders, our employees are inspired by our patient-focused culture to deliver life-changing innovations to those who need them most.