Description

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven environment. This is what we call the Veracyte way  its about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions. 

Our Values:

• We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care
• We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work
• We Are Stronger Together: We collaborate openly, seek to understand, and celebrate our wins
• We Care Deeply: We embrace our differences, do the right thing, and encourage each other

 

The Position:

We are seeking a detail-oriented and highly collaborativeTechnical Writerto support the PMO in documenting processes, frameworks, and project deliverables across Veracytes product development process lifecycle. This role will be instrumental in translating complex technical and operational concepts into clear, accessible documentation that supports cross-functional alignment and regulatory compliance. *Please note this is a temporary 6 month position with potential extension*

Key Responsibilities:  

Develop, review, and maintain regulatory and quality documentation, including:
Technical assessments and validation reports Standard Operating Procedures (SOPs) Business project documents (e.g., charters, plans, status reports)
Collaborate with PMO leaders, Core Team Leads, and subject matter experts to gather information and ensure accuracy. Ensure all documentation complies with relevant regulatory guidelines (e.g., FDA, ISO, GxP) and internal quality standards. Create templates and technical documentation that support PMO operations, including resource management and project tracking. Support audits and inspections by providing accurate and timely documentation. Maintain consistency in style, tone, and formatting across all documentation, adhering to Veracytes standards and branding guidelines. Other consulting duties as assigned.

Location: This is a hybrid/onsite position based in our San Diego location. 

Who You Are:

A minimum of 6 years of proven consulting experience in technical writing within biotech, diagnostics, healthcare, or regulated industries. Strong understanding of regulatory frameworks and quality management systems. Experience with technical assessments, SOPs, and business project documentation. Excellent written and verbal communication skills with a keen eye for detail. Ability to work independently and collaboratively in a fast-paced, matrixed environment. Proficiency in documentation tools and systems (e.g., MS Office, SharePoint). You are a good business partner and a good human

#LI-Onsite, #LI-Hybrid

 

The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to years of experience, skillset, geographic location, industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units.Pay range$56—$63 USD

 

What We Can Offer You

Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified Great Place to Work in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose.

 

About Veracyte

Veracyte (Nasdaq: VCYT) is a global diagnostics company whose vision is to transform cancer care for patients all over the world. We empower clinicians with the high-value insights they need to guide and assure patients at pivotal moments in the race to diagnose and treat cancer. Our Veracyte Diagnostics Platform delivers high-performing cancer tests that are fueled by broad genomic and clinical data, deep bioinformatic and AI capabilities, and a powerful evidence-generation engine, which ultimately drives durable reimbursement and guideline inclusion for our tests, along with new insights to support continued innovation and pipeline development. For more information, please visit www.veracyte.com or follow us on LinkedIn or X (Twitter).

Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our CCPA Disclosure Notice.

If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

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