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15 Hours Ago
Visp, Wallis, CHE
170 Employees
Senior level
170 Employees
Senior level
Biotech
The Sr. Manager of Quality Control at Vaxcyte will coordinate CMC activities related to Quality Control to ensure compliance and secure supply of innovative therapies. Responsibilities include creating QC strategies, maintaining quality control systems, overseeing method validation, managing data accuracy, and reviewing analytical data from contract laboratories.
15 Hours Ago
Visp, Wallis, CHE
Hybrid
170 Employees
Senior level
170 Employees
Senior level
Biotech
The Associate Director of Quality Control oversees the management of CMC activities related to Quality Control for Vaxcyte’s innovative therapies, ensuring compliance with quality standards throughout the development and manufacturing processes. Responsibilities include implementing quality control systems, managing analytical testing methods, and collaborating with contract laboratories.
3 Days Ago
San Carlos, CA, USA
170 Employees
128K-143K Annually
Mid level
170 Employees
128K-143K Annually
Mid level
Biotech
The Scientist II will design and execute in-house assays for polysaccharide analysis, maintain routine operations of analytical instruments, ensure testing compliance, and mentor junior scientists while collaborating with cross-functional teams.
5 Days Ago
San Carlos, CA, USA
Hybrid
170 Employees
241K-268K Annually
Senior level
170 Employees
241K-268K Annually
Senior level
Biotech
The Senior Director of Technical Accounting & SEC Reporting will lead technical accounting and external reporting, ensuring compliance with GAAP and SEC standards. They will oversee the preparation of SEC filings, manage audits, develop policies, collaborate with cross-functional teams, and mentor the accounting team, all while communicating complex topics effectively across the organization.
6 Days Ago
San Carlos, CA, USA
Hybrid
170 Employees
176K-190K Annually
Senior level
170 Employees
176K-190K Annually
Senior level
Biotech
Seeking a Senior Manager, Quality Systems to ensure adherence to regulatory standards and continuous improvement. Responsibilities include implementing GxP systems, supporting regulatory compliance, collaborating with IT and cross-functional teams, monitoring quality metrics, preparing for inspections, and promoting a quality culture.
6 Days Ago
San Carlos, CA, USA
170 Employees
125K-133K Annually
Senior level
170 Employees
125K-133K Annually
Senior level
Biotech
The Scientist I will support analytical activities in the laboratory, assisting in the design and execution of experiments, particularly focusing on analyzing proteins and carbohydrates through various assays and instruments, including HPLC and microplate assays. The role includes method development, data communication, and maintaining detailed experimental records.
6 Days Ago
San Carlos, CA, USA
170 Employees
132K-145K Annually
Entry level
170 Employees
132K-145K Annually
Entry level
Biotech
The Executive Assistant will provide support to the Sr. Vice President, General Counsel & Chief Compliance Officer, and Chief Business Officer. Responsibilities include managing calendars, organizing meetings and travel, preparing materials, and supporting team functions. They will prioritize initiatives, represent the company externally, and assist with various administrative tasks to ensure effective operations.
7 Days Ago
San Carlos, CA, USA
170 Employees
111K-128K Annually
Senior level
170 Employees
111K-128K Annually
Senior level
Biotech
The Senior Associate Scientist will lead the development and optimization of upstream processes for polysaccharide manufacturing using microbial fermentation. Responsibilities include experimental design, execution, and analysis of experiments to enhance yield and quality, performing microbiological work, and maintaining fermentation equipment while collaborating with cross-functional teams and reporting results.
9 Days Ago
San Carlos, CA, USA
170 Employees
152K-170K Annually
Senior level
170 Employees
152K-170K Annually
Senior level
Biotech
The Sr. Scientist in Polysaccharide Analytical Development will design and execute assays for polysaccharide analysis, implement novel platforms, oversee assay automation, ensure quality compliance, and mentor junior scientists. Responsibilities include troubleshooting analytical methods and communicating data effectively across teams.
9 Days Ago
San Carlos, CA, USA
Remote
170 Employees
140K-172K Annually
Mid level
170 Employees
140K-172K Annually
Mid level
Biotech
The Analytical Project Manager at Vaxcyte is responsible for overseeing analytical activities related to clinical products, providing scientific support, drafting protocols, and managing project timelines to ensure milestones are met according to quality standards. This role requires coordination between CMC and program team members, guiding key documentation, and addressing potential risks in a timely manner.
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