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Stability Manager

VaxcyteSan Carlos, California, United States
On-site Full-time $147K/yr - $171K/yr

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Experience Level

Manager

Qualifications

Essential Functions:Design, coordinate, and execute stability studies for early and late-stage vaccine products in accordance with regulatory guidelines and company protocols. Manage stability data analysis to ensure product integrity throughout development. Collaborate with cross-functional teams to ensure compliance with quality standards. Foster a culture of open communication and data-driven decision-making.

About the job

Join Our Mission to Safeguard Humanity!

Vaxcyte is a pioneering clinical-stage vaccine innovation company dedicated to engineering high-fidelity vaccines aimed at protecting humanity from the dire consequences of bacterial diseases. Our mission to combat and eradicate bacterial infections—including invasive pneumococcal disease, Group A Strep, and Shigella—is just the beginning. With a clear and defined path to success, Vaxcyte is positioned to make a lasting impact.
 
Our Approach: At Vaxcyte, what we do is as crucial as how we achieve it. Our work is guided by four core values:
 
*RETHINK CONVENTION: We leverage creative and intellectual diversity to innovate and redefine the delivery of vaccines.
 
*AIM HIGH: We pursue our ambitious goal of developing the most complex biologics ever attempted for the protection of humanity.
 
*LEAD WITH HEART: At Vaxcyte, we prioritize kindness and inclusivity in our collaborative efforts, fostering vigorous discussions that align with our business objectives.
 
*MODEL EXCELLENCE: Our shared challenge necessitates a commitment to integrity, accountability, equality, and clarity in all communications and decisions.

Summary:

Vaxcyte is seeking a dynamic and skilled individual to join our Vaccine Product Development team as a Stability Manager within the Quality Control Unit. This role is vital for managing the stability program for various projects in preclinical and clinical development.

In this position, you will play an essential role in implementing and upholding cGMP Stability for all stages of clinical development. Your primary responsibilities will include overseeing stability studies for individual projects and analyzing stability data. You will collaborate closely with QC team members in a highly cooperative and cross-functional environment. The ideal candidate will bring extensive stability experience, ensure compliant operations and documentation, promote open communication, and adopt data-driven methodologies.

About Vaxcyte

Vaxcyte is at the forefront of vaccine innovation, focusing on developing advanced vaccines to tackle bacterial diseases that pose significant health risks. Our vision is to create high-fidelity vaccines that not only address current health challenges but also pave the way for future advancements in vaccine technology.

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