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10 Days Ago
San Carlos, CA, USA
Hybrid
170 Employees
100K-161K Annually
Senior level
170 Employees
100K-161K Annually
Senior level
Biotech
The Payroll Manager at Vaxcyte will oversee all payroll processes, maintaining compliance with tax laws and company policies, and facilitating employee onboarding and offboarding. Duties include payroll preparation, tax withholding management, participation in month-end close processes, and automation of payroll and stock administration processes for efficiency. The role also involves employee education and collaboration on projects related to accounting and regulatory audits.
10 Days Ago
San Carlos, CA, USA
Hybrid
170 Employees
185K-195K Annually
Senior level
170 Employees
185K-195K Annually
Senior level
Biotech
The Associate Director of Quality Control will manage global reference standards and critical reagents, ensuring compliance with ICH guidelines. They will lead policy development, oversee technical documentation, and collaborate with CMC, QA, and RA teams for clinical and commercial product testing and release.
10 Days Ago
San Carlos, CA, USA
170 Employees
130K-150K Annually
Junior
170 Employees
130K-150K Annually
Junior
Biotech
Vaxcyte is seeking a Scientist II, Conjugation Development to contribute to process characterization efforts for pneumococcal conjugate vaccine program and work on conjugation process development for pipeline programs. Responsibilities include preparation, purification, and analytical characterization of chemically modified polysaccharides and polysaccharide-protein conjugates.
10 Days Ago
San Carlos, CA, USA
170 Employees
125K-130K Annually
Senior level
170 Employees
125K-130K Annually
Senior level
Biotech
The Sr. Associate Scientist will contribute to the research and development of a novel bacterial polysaccharide conjugate vaccine, focusing on developing and optimizing scalable purification processes. Responsibilities include utilizing various chromatography techniques, analyzing polysaccharides, maintaining laboratory records, and collaborating with internal and external teams.
10 Days Ago
San Carlos, CA, USA
170 Employees
145K-162K Annually
Senior level
170 Employees
145K-162K Annually
Senior level
Biotech
The Sr. Scientist in Analytical Development will lead the development and qualification of analytical methods for vaccine targets. Responsibilities include developing methods, conducting characterization studies, overseeing CRO/CMO collaborations, and authoring protocols and reports while mentoring junior team members.
10 Days Ago
San Carlos, CA, USA
Hybrid
170 Employees
144K-162K Annually
Senior level
170 Employees
144K-162K Annually
Senior level
Biotech
The Group Leader in Analytical Development will manage a team focused on R&D stability studies and assay control qualification. Responsibilities include lab operations oversight, technical mentorship, experiment design, data communication, and ensuring compliance and quality in testing processes.
10 Days Ago
San Carlos, CA, USA
Hybrid
170 Employees
144K-162K Annually
Senior level
170 Employees
144K-162K Annually
Senior level
Biotech
The Stability Manager will oversee the stability program within Vaxcyte's Vaccine Product Development, managing stability studies, analyzing stability data, and ensuring compliance with regulatory guidelines. This role requires collaboration with cross-functional teams and involves developing stability protocols, creating reports, and presenting findings to ensure project milestones are met.
17 Days Ago
San Carlos, CA, USA
170 Employees
73K-91K Annually
Entry level
170 Employees
73K-91K Annually
Entry level
Biotech
The Associate Engineer I will support the polysaccharide development and manufacturing group by conducting downstream process development experiments, operating laboratory equipment, conducting assays, maintaining records, and participating in technical discussions while collaborating with the CMC team.
19 Days Ago
San Carlos, CA, USA
Hybrid
170 Employees
180K-187K Annually
170 Employees
180K-187K Annually
Not Specified
Biotech
Seeking a Sr. Manager for Quality Control Reference Standards team to oversee management and supply of reference standards for clinical and commercial products. Ensure compliance with global regulatory guidelines and support pipeline of high-fidelity vaccines.
23 Days Ago
San Carlos, CA, USA
Hybrid
170 Employees
115K-124K Annually
Junior
170 Employees
115K-124K Annually
Junior
Biotech
The Document Control Specialist at Vaxcyte is responsible for managing and maintaining quality systems documentation related to vaccine manufacturing in a GXP compliant environment. This role involves overseeing the lifecycle of GMP documents in Veeva, collaborating with quality assurance and project management teams, and supporting audits while ensuring compliance with regulatory standards.
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