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Manual qa tester Jobs in San Mateo, CA

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Manual qa tester • san mateo ca

Last updated: 2 days ago
  • Promoted
Director- QA Compliance

Director- QA Compliance

Gilead Sciences, Inc.Foster City, CA, US
Full-time
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...Show moreLast updated: 6 days ago
  • Promoted
Sr. IVD QA Manager

Sr. IVD QA Manager

VeracyteSouth San Francisco, CA, US
Full-time
At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe.Working at Veracyte...Show moreLast updated: 30+ days ago
Project Coordinator - QA / QC

Project Coordinator - QA / QC

Tutor PeriniMenlo Park, CA, United States
Full-time
Expected hourly rate for this position is $30.Rudolph & Sletten, a Tutor Perini Company, is seeking a • •Project Coordinator - QAQC • • to join our project office in Palo Alto, CA.About Rudolph & Sl...Show moreLast updated: 15 days ago
Test Technician, QA

Test Technician, QA

ICONMAFoster City, CA
Full-time
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...Show moreLast updated: 12 days ago
  • Promoted
QA Specialist III

QA Specialist III

Gilead SciencesSan Mateo, CA, United States
Full-time +1
At Gilead, were creating a healthier world for all people.For more than 35 years, weve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer working relentlessly to develop therapies t...Show moreLast updated: 2 days ago
  • Promoted
QA Engineering Lead

QA Engineering Lead

MetaMenlo Park, CA, US
Full-time
We're looking for QA Engineering Leads to work on our core and business products (ex.Facebook, Instagram, Messaging Apps ) to help shape the future of what we build at Facebook.You will enjoy solvi...Show moreLast updated: 30+ days ago
Online Product Tester

Online Product Tester

Online Consumer Panels AmericaDaly City, California, US
Part-time +1
Product Testers are wanted to work from home nationwide in the US to fulfill upcoming contracts with national and international companies. We guarantee 15-25 hours per week with an hourly pay of bet...Show moreLast updated: 30+ days ago
QA Manager

QA Manager

Infospan IncFoster City, CA, California, USA
Full-time
Title : QA Manager- Location : On Site - Foster City, CA Experi...Show moreLast updated: 30+ days ago
Senior QA Producer

Senior QA Producer

31st UnionSan Mateo, CA, United States
Full-time
We are a diverse team of developers driven by a passion for our art, united by our core values and inspired by a culture of inclusivity to build amazing games that thrill players everywhere.We purs...Show moreLast updated: 14 days ago
Project Coordinator - QA / QC

Project Coordinator - QA / QC

Tutor Perini CorporationMenlo Park, CA, United States
Full-time
Expected hourly rate for this position is $30.Rudolph & Sletten, a Tutor Perini Company, is seeking a Project Coordinator - QAQC to join our project office in Palo Alto, CA.About Rudolph & Sletten : ...Show moreLast updated: 16 days ago
Director of Clinical QA

Director of Clinical QA

Dren BioFoster City, California, United States
Full-time
Dren Bio (the "Company") is a privately held, clinical stage biopharmaceutical company focused on developing therapeutic antibodies for the treatment of cancer, autoimmune and other serious disease...Show moreLast updated: 30+ days ago
QA Lead Coordinator.

QA Lead Coordinator.

Games Jobs DirectSan Mateo, United States
Full-time +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...Show moreLast updated: 30+ days ago
QA Training Specialist

QA Training Specialist

Gilead Sciences, Inc.Foster City, California, United States
Full-time
Manages the development and implementation of learning programs to meet compliance goals, development needs, and operational excellence initiatives. Supports the coordination of training sessions in...Show moreLast updated: 12 days ago
QA Supervisor - ASL

QA Supervisor - ASL

Ahtna, Inc.Daly City, CA, United States
Full-time
SummaryThe Quality Assurance (QA) Supervisor is a position that oversees the daily quality operations and ensures that processes comply with project and stakeholder standards.This individual superv...Show moreLast updated: 30+ days ago
  • Promoted
Director Pharmacovigilance QA

Director Pharmacovigilance QA

Meet Life SciencesRedwood City, CA, United States
Full-time
Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features.Direct message the job poster from Meet Life Sciences Senior Client Partner | Master of Science in Pha...Show moreLast updated: 18 days ago
Senior QA Engineer

Senior QA Engineer

RobinhoodMenlo Park, CA
Full-time
Join a leading fintech company that’s democratizing finance for all.Robinhood Markets was founded on a simple idea : that our financial markets should be accessible to all.With customers at the hear...Show moreLast updated: 8 days ago
QA Lead

QA Lead

Propel LondonSAN MATEO
Permanent
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...Show moreLast updated: 30+ days ago
  • Promoted
Paid Product Tester

Paid Product Tester

Product Review JobsBURLINGAME, CA, United States
Full-time
Compensation : Varies per assignment.Location : Remote (USA) Company : ProductReviewJobs Thank you for your interest in becoming a Paid Product Tester. This opportunity is for completing market res...Show moreLast updated: 14 days ago
People also ask
Director- QA Compliance

Director- QA Compliance

Gilead Sciences, Inc.Foster City, CA, US
6 days ago
Job type
  • Full-time
Job description

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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