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 – it’s 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 otherThe Position:
We are seeking a detail-oriented and highly collaborative Technical Writer to support the PMO team in documenting processes, frameworks, and project deliverables across Veracyte’s 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 3 month position with potential extension*
This is a hybrid position based in our San Diego, CA office. Based on candidate location, we may consider (PST) remote.
Monday-Friday, 8AM-5PM.
Key Responsibilities:
Collaborate with PMO leaders, Core Team Leads, and subject matter experts to document product development processes (PDP), project governance models, and stage gate frameworks Write user-friendly content that meets the needs of target audience, turning insights into language for user success Create templates, SOPs, and technical documentation that support PMO operations, including PDP, resource management, and project tracking Ensure consistency in style, tone, and formatting across all PMO documentation, adhering to Veracyte’s internal standards and branding guidelines Other duties as assignedLocation: This is a hybrid/onsite position based in our San Diego, CA location. Based on candidate location, we may consider (PST) remote.
Who You Are: Minimum of 7 years of proven experience in technical writing within biotech, diagnostics, or healthcare industries. Experience with product development processes, regulatory documentation, and project management methodologies. Proven ability to quickly learn and understand complex subject matter Excellent written and verbal communication skills with a keen eye for detail. Ability to work independently and collaboratively in a fast-paced, matrixed environment. High School degree or equivalent degree required.#LI-Hybrid
The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the 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. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.
Pay range$56—$63 USDWhat 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 genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide. Veracyte is based in South San Francisco, California. For more information, please visit www.veracyte.com and follow the company on X (Formerly 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.
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