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

Competition
Low
0.194338
Based on job seekers per open jobs
Desired Skills
Years of Experience
Years of Experience distribution graph for Quality Specialists in San Francisco-Oakland-San Jose. Quality Specialists in San Francisco-Oakland-San Jose have between ${} and ${} years of experience, averaging $${} years of experience.

17 Quality Specialist jobs in San Francisco-Oakland-San Jose

Berkeley, CA
In this role, you will acts to ensure that the manufacturing and QC method/standard review process is consistent with company policy and industry/regulatory expectations.
industry
Biotech/Pharma
experience
8 - 10 years

San Jose, CA
In this role, you will review changes to Corporate procedures and assess the impact on local site procedures. Revise site procedures as necessary to maintain compliance.
industry
Medical Devices & Diagnostics
experience
11 - 15 years

San Mateo, CA
In this role, you will be responsible for maintains and enforces a compliant and effective QMS for the activities in scope, as well as for effective and lean QMS structures and Q&R processes.
industry
Energy & Environmental Services
experience
Not Specified

Rancho Cordova, CA
The Coding Quality Coordinator, Sr., is the advanced skill level position responsible for performing complex reviews of physician clinical documentation on inpatient and outpatient medical records.
industry
Healthcare IT
experience
5 - 7 years

San Jose, CA
In this role, you will facilitate development and maintainence of the quality management system according to ISO, MDD and FDA requirements.
industry
Medical Devices & Diagnostics
experience
5 - 7 years

Sunnyvale, CA
In this role, you will be independently reviews and approves master batch records, labels, specifications, and other manufacturing documents of clinical and commercial drug substances and drug products in compliance with all applicable requirements.
industry
Biotech/Pharma
experience
Less than 5 years

Berkeley, CA
In this role, you will provide Quality oversight and guidance to internal and external customers to ensure a compliant EM program and to ensure the program is consistent with company procedures.
industry
Biotech/Pharma
experience
5 - 7 years

Burlingame, CA
In this role, the selected candidate will able to communicate and work well on tasks with ancillary and ad hoc team members, community partners and stakeholders (including local health agencies) to plan, facilitate, and execute activities.
industry
Healthcare IT
experience
Less than 5 years

Redwood City, CA
This position is responsible for administering aspects of the Quality Management System related to quality system compliance and continuous improvement. The ideal candidate will have a Quality Specialist/Engineering background in a medical device/in-vitro diagnostic, or molecular reagent company.
industry
Biotech/Pharma
experience
5 - 7 years

Fremont, CA
In this role, you will review changes to Corporate procedures and assess the impact on local site procedures. Revise site procedures as necessary to maintain compliance.
industry
Medical Devices & Diagnostics
experience
11 - 15 years

San Francisco, CA
In this role, you will responsible for implementing optimization, along with quality assurance, during pre-launch stage, to ensure successful onboarding of advertisers.
industry
Consulting
experience
5 - 7 years

Burlingame, CA
The Quality Improvement Specialist, HAI will have knowledge and expertise in infection prevention practices. They will provide consultation, education, and technical program support informing infection preventionists at hospitals enrolled in the CalHIIN, which is part of The Centers for Medicare & Medicaid Services (CMS) Partnership for Patients (PfP) Initiative.
industry
Healthcare IT
experience
Less than 5 years

Fremont, CA
In this role, you will provide guidance to other QC functions to ensure compliance with all applicable regulations and assists in resolution of issues identified.
industry
Biotech/Pharma
experience
5 - 7 years

San Francisco, CA
In this role, the successful candidate will perform BSA/AML, sanctions, FCPA, and fraud related testing at the Enterprise level, business or support units, and bank subsidiaries.
industry
Financial Services
experience
Less than 5 years

Fremont, CA
In this role, you will serve as Subject Matter Expert for internal or external matters. Participates in inspection readiness activities and significantly involved in inspections by regulatory agencies.
industry
Business Services
experience
8 - 10 years

Sunnyvale, CA
In this role, you will develop CQA plans and implements the actions necessary to ensure clinical trials are conducted in accordance with the audit plan, GCP guidelines and regulatory requirements.
industry
Biotech/Pharma
experience
5 - 7 years

Union City, CA
In this role, you will maintain current knowledge of FDA and applicable international policies and regulations that may affect the company's products and customers.
industry
Medical Devices & Diagnostics
experience
8 - 10 years