Job Market Guide: Director of Quality jobs in San Francisco-Oakland-San Jose

Competition
High
0.717507
Based on job seekers per open jobs
Desired Skills
Years of Experience
Years of Experience distribution graph for Director of Qualitys in San Francisco-Oakland-San Jose. Director of Qualitys in San Francisco-Oakland-San Jose have between ${} and ${} years of experience, averaging $${} years of experience.

38 Director of Quality jobs in San Francisco-Oakland-San Jose

Fremont, CA
Develop and maintain compliant quality system that adheres to FDA regulatory expectations both internally and with respect to oversight of the companys suppliers.
industry
Biotech/Pharma
experience
11 - 15 years

Brisbane, CA
Develop, implement and maintain quality assurance documentation systems, procedures, and compliance programs that support all Aimmune products.
industry
Biotech/Pharma
experience
11 - 15 years

$130K - $200K - San Francisco, CA
The candidate will develop inspection strategies and process improvement plans related to Clinical Operations activities and will provide senior management with in-depth analysis and risk management on GCP QA related matters.
industry
Biotech/Pharma
experience
11 - 15 years

Fremont, CA
Develop multi-year vision and objectives for the information systems to support industry leading performance in Safety and Quality.
industry
Semiconductors
experience
11 - 15 years

QA Director

Mountain View, CA
You will be intimately involved with the development team, testing products, services, changes, etc., both on our development and our live servers, and in multiple browsers.
industry
Business Services
experience
Not Specified

Pleasanton, CA
Ensures that all processes needed for the Corporate Quality Management System are established, implemented and maintained, including but not limited to: CAPA, complaint handling, design control, documentation control, internal audit, management review, nonconforming product, production and process controls, MDR, and field corrective actions.
industry
Healthcare IT
experience
5 - 7 years

$140K - $170K - Menlo Park, CA
Review and approve lot packages and QC data nonclinical, clinical and commercial products to ensure CMO/CRO manufacturing and analytical testing are performed in accordance with applicable company procedures and are in compliance with all applicable regulatory requirements; disposition product lots per company procedures.
industry
Biotech/Pharma
experience
8 - 10 years

San Francisco, CA
In this role, the selected candidate will provide clinical oversight on the development and monitoring of system/programs to evaluate care quality and outcomes.
industry
Patient Care
experience
Less than 5 years

San Francisco, CA
The Director of Quality Engineering will oversee all things quality related at company and report to the Head of Engineering.
industry
IT Consulting/Services
experience
11 - 15 years

$140K - $170K - Palo Alto, CA
Review and approve lot packages and QC data nonclinical, clinical and commercial products to ensure CMO/CRO manufacturing and analytical testing are performed in accordance with applicable company procedures and are in compliance with all applicable regulatory requirements; disposition product lots per company procedures.
industry
Biotech/Pharma
experience
8 - 10 years

Santa Clara, CA
Interfaces with both internal groups (such as Design, Process R&D, Applications and Marketing), as well as external customers for product quality issues.
industry
Semiconductors
experience
5 - 7 years

$140K - $170K - San Mateo, CA
Review and approve lot packages and QC data nonclinical, clinical and commercial products to ensure CMO/CRO manufacturing and analytical testing are performed in accordance with applicable company procedures and are in compliance with all applicable regulatory requirements; disposition product lots per company procedures.
industry
Biotech/Pharma
experience
8 - 10 years

San Francisco, CA
Assess compliance with BSA/sanctions related regulations and established Bank policies and procedures and identify any potential and emerging BSA/sanctions/fraud risks or issues.
industry
Financial Services
experience
5 - 7 years

San Francisco, CA
The Compliance Director for Pharmacovigilance (PV) is a global role that is responsible for Amgens PV compliance program worldwide, leads a team of PV compliance professionals, and serves as the company expert on compliance with global PV requirements.
industry
Biotech/Pharma
experience
Not Specified

$185K - $210K - San Francisco, CA
This individual will have written standard operating procedures, systems and processes, have experience working with CROs and clinical sites and be an experienced auditor. As this individual will provide training on GCP, excellent communication skills and an engaging personality are recommended.
industry
Business Services
experience
11 - 15 years

San Jose, CA
you will collaborate with product managers, directors, managers, software engineers and data center operations engineers in the creation of products.
industry
Business Services
experience
5 - 7 years

Santa Clara, CA
Build a strong technical culture by encouraging and empowering our teams to produce industry changing QA engineering practices.
industry
Information Services
experience
11 - 15 years

$190K - $225K - South San Francisco, CA
Support validation activities related to facility, equipment, process, and computerized systems. Compile Quality Metrics for all manufactured commercial drug substance and drug product manufactured, and report these on a regular basis to Management.
industry
Biotech/Pharma
experience
15+ years

FOSTER CITY, CA
Identify current and future product gaps based on user feedback as well as new payment.
industry
Business Services
experience
Not Specified

$140K - $170K - Redwood City, CA
Review and approve lot packages and QC data nonclinical, clinical and commercial products to ensure CMO/CRO manufacturing and analytical testing are performed in accordance with applicable company procedures and are in compliance with all applicable regulatory requirements; disposition product lots per company procedures.
industry
Biotech/Pharma
experience
8 - 10 years

$140K - $170K - San Francisco, CA
Review and approve lot packages and QC data nonclinical, clinical and commercial products to ensure CMO/CRO manufacturing and analytical testing are performed in accordance with applicable company procedures and are in compliance with all applicable regulatory requirements; disposition product lots per company procedures.
industry
Biotech/Pharma
experience
8 - 10 years