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

Competition
High
0.714066
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.

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

Berkeley, CA
Identify and evaluate issues of significance, communicating complex issues to quality leadership, providing multiple alternatives to the solution of complex problems and is able to provide guidance in their implementation.
industry
Business Services
experience
8 - 10 years

San Francisco, CA
Hire, lead and manage a quality organization within Docker Engineering that is second to none. Define and implement quality strategy across all of company's products.
industry
Business Services
experience
11 - 15 years

San Jose, CA
Collaborate with project managers, development team and customers on Functional Safety across SANM automotive organization; ensure effective communication and containment of quality issues identified by customers.
industry
Manufacturing / Diversified
experience
11 - 15 years

San Francisco, CA
Write and maintain SOPs pertaining to SSF QA function in alignment with PMQA processes.
industry
Biotech/Pharma
experience
5 - 7 years

$130K - $190K - San Francisco, CA
Provide leadership and direction to a compliance team, and will be responsible for the selection and management of the personnel for the achievement of the department's goals.
industry
Retail / Health & Pharmacy
experience
11 - 15 years

$140K - $170K - San Jose, 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
As the leader of GBTs Clinical QA function, this individual will serve as a strategic and tactical quality professional in managing compliance related to GCPs, pharmacovigilance and other related activities. The individual will be a critical team member who designs and implements risk-based GCP audit programs and compliance oversight.
industry
Business Services
experience
8 - 10 years

Hayward, CA
Provides effective leadership in recruiting and developing team members to meet the requirements of a commercial quality organization. Defines procedures for the training and qualification of analysts/supervisors and ensures all are trained and qualified accordingly.
industry
Healthcare IT
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

$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

Newark, CA
Beyond assuring quality in current product development efforts, collect, feedback, and lead efforts to identify the shortcomings in existing products and craft solutions ahead of the next products iteration.
industry
Hardware
experience
11 - 15 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
Responsible for executing Quality Assurance (QA) programs and activities; this includes assisting with training and auditing programs, as well as the review of SOPs, investigations, specifications, methods, reports and manufacturing records.
industry
Patient Care
experience
11 - 15 years

San Jose, CA
As the Software Quality Director, youll be working with some of the industrys brightest minds to define and design the vehicle quality assurance plan. Basically, youll make sure that the infotainment system works accordingly.
industry
Automotive
experience
11 - 15 years

$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

South San Francisco, CA
The incumbent is responsible for executing on policies, procedures and systems to support development activities in compliance to Theravance quality standards and applicable GCP requirements.
industry
Biotech/Pharma
experience
8 - 10 years

San Jose, CA
Work with Software Engineering, Product Management, Operations, and Program Management to design testing strategies ensure that products are thoroughly tested before they are shipped, and to ensure smooth product launches and customer satisfaction.
industry
Telecommunications
experience
5 - 7 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

Hayward, CA
Provide general compliance oversight and operations ensuring compliance with regulatory requirements and standard operating procedures.
industry
Healthcare IT
experience
11 - 15 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

$140K - $170K - Mountain View, 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