Join our Mission to Protect Humankind!
Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, periodontitis and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.
WHAT we do is every bit as important as HOW we do it! Our work together is guided by four enduring core values:
*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.
*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.
*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.
*MODEL EXCELLENCE: The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.
Summary:
Vaxcyte seeks an energetic and talented individual with profound experience in reference standards and critical reagent management to join our quality control team as an Associate Director/Senior QC Manager. The position will be an integral part of the team responsible for cGMP compliance in routine operations for all phases of clinical development and commercial for Vaxcyte vaccine programs.
The successful candidate will report to the Senior Director of QC, be part of the Quality Control Extended Leadership team, and establish policy and strategy in managing the reference standards and critical reagents in compliance with ICH guidelines. The successful candidate must demonstrate strong reference standard management skills and statistical and technical knowledge, be familiar with basic scientific/regulatory principles, possess initiative, and maintain a solid commitment to quality, compliance, and scientific excellence.
This position will establish and maintain the global program management of reference standards and critical reagents for testing and releasing clinical and commercial products. This position will collaborate with internal CMC, QA, and RA functional teams and external partners (CDMOs/CTLs) to ensure the global network's continuous supply of qualified Reference Standards and Critical Reagents.
Reports to: Senior Director, ASAT for Quality Control
Location: San Carlos, CA
Compensation:
The compensation package will be competitive and includes comprehensive benefits and an equity component.
Salary Range: $185,000 – $195,000
Send resumes to:
Vaxcyte, Inc.
825 Industrial Road, Suite 300
San Carlos, CA 94070
We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.