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Qa • san mateo ca

Última actualización: hace 6 horas
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Director- QA Compliance

Director- QA Compliance

Gilead Sciences, Inc.Foster City, CA, US
A tiempo completo
At Gilead, we're creating a healthier world for all people.For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19, and cancer – working relentlessly to develop therap...Mostrar másÚltima actualización: hace más de 30 días
Test Technician, QA

Test Technician, QA

ICONMAFoster City, CA
A tiempo completo
Our Client, an Av Manufacturing company, is looking for a Test Technician, QA for their Foster City, CA location.Conduct basic software operation tasks. Support missions through a wide variety of ro...Mostrar másÚltima actualización: hace más de 30 días
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Senior Manager, GxP QA Auditor

Senior Manager, GxP QA Auditor

REVOLUTION MedicinesRedwood City, CA, United States
A tiempo completo
Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company's R&D pipeline com...Mostrar másÚltima actualización: hace 5 días
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QA Release Engineer

QA Release Engineer

Vertex Sigma SoftwareFoster City, California, United States
A tiempo completo
As a QA / Release Engineer, you will play a critical role in our software quality and delivery by driving process improvements to release our vehicle software regularly, reliably, and with high qua...Mostrar másÚltima actualización: hace 4 días
Software QA Engineer

Software QA Engineer

Playstation GlobalSan Mateo, California, United States
A tiempo completo
PlayStation isn’t just the Best Place to Play — it’s also the Best Place to Work.Today, we’re recognized as a global leader in entertainment producing The PlayStation family of products and service...Mostrar másÚltima actualización: hace 10 días
QA Manager

QA Manager

Infospan IncFoster City, CA, California, USA
A tiempo completo
Title : QA Manager- Location : On Site - Foster City, CA Experi...Mostrar másÚltima actualización: hace más de 30 días
  • Oferta promocionada
  • Nueva oferta
Senior Manager, GxP QA Auditor

Senior Manager, GxP QA Auditor

Revolution MedicinesRedwood City, CA, US
A tiempo completo
Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers.The company's R&D pipeline...Mostrar másÚltima actualización: hace 22 horas
Test Technician, QA

Test Technician, QA

UrsusFoster City, CA
A tiempo completo
Individual compensation is determined by skills, qualifications, experience, and location.Compensation details listed in this posting reflect the base hourly rate or annual salary only, unless othe...Mostrar másÚltima actualización: hace 17 días
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Technical Program Manager - Product Software QA

Technical Program Manager - Product Software QA

ZooxSan Mateo, CA, United States
A tiempo completo
Zoox has embarked on a highly ambitious journey to develop a full-stack autonomous mobility solution for our cities.As a technical program manager, you will work cross-functionally with engineering...Mostrar másÚltima actualización: hace 6 días
QA Lead Coordinator.

QA Lead Coordinator.

Games Jobs DirectSan Mateo, United States
A tiempo completo +1
Every day, tens of millions of people come to Roblox to explore, create, play, learn, and connect with friends in 3D immersive digital experiences- all created by our global community of developers...Mostrar másÚltima actualización: hace más de 30 días
QA Training Specialist

QA Training Specialist

Gilead SciencesFoster City, California, United States
A tiempo completo
At Gilead, we’re creating a healthier world for all people.For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapi...Mostrar másÚltima actualización: hace más de 30 días
Associate QA Analyst

Associate QA Analyst

IXLSan Mateo, CA
A tiempo completo
IXL Learning, developer of personalized learning products used by millions of people globally, is seeking an Associate QA Analyst focused on UI and front end testing. The ideal candidate will have a...Mostrar másÚltima actualización: hace más de 30 días
Lead QA (F / H)

Lead QA (F / H)

Groupe Bayardundefined, undefined
Au sein de la Digital Factory de la Direction Technologie Data & Digital, composée d’équipes en charge de la conception, du développement et de la maintenance de sites web, applications mobiles...Mostrar másÚltima actualización: hace 3 días
QA Test Engineer

QA Test Engineer

Aechelon TechnologySouth San Francisco, California, United States
A tiempo completo
D simulator content, including Geospecific visual / sensor databases and realistic 3D models.We seek people who share our passion for real-time computer graphics and commitment to our mission of help...Mostrar másÚltima actualización: hace más de 30 días
Senior Software QA Engineer

Senior Software QA Engineer

Culture BiosciencesSouth San Francisco, California, United States
A tiempo completo
Culture’s mission is to simplify and accelerate bioprocess development to help our customers bring biopharmaceutical products to market faster. Focusing on upstream cell culture process development,...Mostrar másÚltima actualización: hace 19 días
  • Nueva oferta
AI Engineer - Platform QA

AI Engineer - Platform QA

Ebates Performance MarketingSan Mateo, California, USA
A tiempo completo
Rakuten International is a division of Rakuten Group Inc.Japanese global technology leader in services that empower individuals communities businesses and society. Headquartered in San Mateo Califor...Mostrar másÚltima actualización: hace 6 horas
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  • Nueva oferta
Software QA Engineer

Software QA Engineer

OSI EngineeringMenlo Park, CA, US
A tiempo completo
We’re looking for a skilled Software Quality Assurance Engineer to join our team and collaborate alongside Product and Engineering team members. This role will focused on supporting both web and mob...Mostrar másÚltima actualización: hace 8 horas
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Salesforce QA Tester

Salesforce QA Tester

StaffingSan Mateo, CA, US
A tiempo completo
Bachelor's degree in Computer Science or related field of study.Quality Assurance experience with 4 years of exclusive SFDC QA experience. Jira, Selenium and other tools.Should be a certified Salesf...Mostrar másÚltima actualización: hace 26 días
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Netflix QA Tester

Netflix QA Tester

TradeJobsWorkforce94128 South San Francisco, CA, US
A tiempo completo
Help us succeed as our next Netflix QA Tester to perform responsibilities as a QA Tester.Stay adaptable to changing priorities and business needs. Stay adaptable to changing priorities and business ...Mostrar másÚltima actualización: hace 16 días
QA Lead

QA Lead

Propel LondonSAN MATEO
Indefinido
As a QA automation Tech Lead you will provide thought leadership to the business's already well-established Automation Engineering team. You will provide expertise, support and leadership to a numbe...Mostrar másÚltima actualización: hace más de 30 días
Director- QA Compliance

Director- QA Compliance

Gilead Sciences, Inc.Foster City, CA, US
Hace más de 30 días
Tipo de contrato
  • A tiempo completo
Descripción del trabajo

Job Description

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19, and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination, and a relentless drive to make a difference.

Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed, and empowered to fulfill their aspirations. Join Gilead and help create possible, together.

Job Description

The Director- QA Compliance, will report to the Executive Director of Supplier Management and Auditing. This key position will be the acting Global Process Owner for External Audits and conduct GMP audits of Gilead's global suppliers with a primary focus on external biologics manufacturing, contract packaging, and contract testing labs. This position will lead audits to support the effectiveness of the global audit program and will work closely with cross-functional partners and internal stakeholders.

  • Lead the development, implementation, and maintenance of procedures and templates to assist in the evaluation of and in improvement of the auditing process.
  • Develop strategy for cross training and maintenance of auditor and SME qualifications.
  • Assist in overall scheduling and productivity / capacity modeling for audit team.
  • Identify compliance risks and escalate issues to appropriate levels of management for resolution.
  • Promote awareness across the biologics commercial and clinical manufacturing platform(s) of current regulatory agency requirements and trends and develop and report on the trends identified to better focus the scope of audits.
  • Align, strategize and collaborate with the Global Supplier Quality function within Gilead.
  • Enhance Global Third party Quality Oversight program and Qualification Process by leading initiatives to maintain compliance to global regulations and standards.
  • Represent the Quality function by developing the program and supporting the selection process for new / preferred suppliers.
  • Act as liaison between global supplier quality and Gilead's production facilities.
  • Conduct global vendor audits for contract manufacturing of Gilead Biologics.
  • Support and / or conduct audits of providers of raw materials, product contact consumables, contract manufacturing or testing, software, warehouse / distribution in support of Gilead's clinical and commercial oral and parenteral dosage formulations and associated medical devices as assigned.
  • Manage all aspects of the audit lifecycle including scheduling, planning, issuing agendas, executing, issuing reports, evaluating responses, requesting clarification, issuing CA / PA, and closing.
  • Drive consistency with audit report observation writing, classification, status, and overall risk.
  • Conduct due diligence assessments as part of global expansion as required.
  • Identify and drive biologics audit program improvements and meet all required metrics and assigned goals.
  • Ensure CA / PA to address compliance concerns identified during audits are commensurate with current biologics industry practices and benchmarks.
  • Ensure that the audit agenda is risk-based and has the appropriate internal and / or external subject matter experts as part of the audit team.
  • Work directly with Gilead cross-functional departments to gather key information and feedback prior to conducting vendor audits in order to ensure effectiveness.

Travel is required up to 50%

This will be an on-site role, and can be located in Foster City, CA OR Parsippany, NJ

Essential Functions :

  • Supports Compliance management in maintaining the company's Compliance program.
  • Manages the day-to-day activities of one or more individual contributors, including task assignment and prioritization, monitoring task performance, and conducting performance reviews.
  • Ensures awareness of biologics compliance requirements across impacted functional areas.
  • Establishes excellent working relationships with compliance / quality groups.
  • Responsible for maintaining current knowledge of applicable compliance requirements through attendance at industry and regulatory agency sponsored meetings and seminars and individual self-study including periodic review of all relevant regulations, guidance documents, and requirements.
  • Responsible for providing guidance on interpretation and application of existing and new requirements. Provide guidance to assigned departments and management when specific compliance issues arise.
  • Assists in evaluation and implementation of standard operating procedures and systems needed to comply with requirements.
  • Leads various types of audits or projects or supervises contractors. Audits may include internal systems audits, external vendor audits, or document reviews.
  • Assists in regulatory agency inspections. Assists in coordination of responses to any regulatory agency findings.
  • Basic Qualifications :

  • 10+ years of relevant experience in the pharmaceutical industry and a BS or BA in a relevant field of study.
  • 8+ years of relevant experience and a MS in a relevant field of study.
  • Extensive background in Biologics Operations (e.g. Manufacturing, Quality Control, Quality Assurance).
  • Demonstrates excellent verbal, written, and interpersonal skills.
  • Demonstrates a thorough knowledge of compliance requirements, and an understanding of current global and regional trends in compliance.
  • Knowledge of domestic and international regulations including 21 CFR Parts 11, 203, 205. 210, 211, 600, 610, 820; EudraLex Volume 4 and applicable annexes; and Health Canada R.S.C., 1985, F-27, Section 30; as well as ICH, ISO, PIC / S and USP / NF, EP, and JP compendial standards and principles as applicable.
  • Skilled auditor with 10 years of experience and ability to perform investigative audits.
  • Is capable of taking a leadership role in updating and preparing the company for changes in regulations.
  • Is capable of leading a small team in development of systems and procedures and implementation.
  • Is well recognized as a knowledgeable resource for QA compliance advice in other departments.
  • Capable of effectively managing a small team of experienced subject matter experts in execution of audits.
  • The salary range for this position is : $210,375.00 - $272,250.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans.

    For additional benefits information, visit : https : / / www.gilead.com / careers / compensation-benefits-and-wellbeing

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