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Part-time Quality assurance Jobs in San Mateo, CA

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Quality assurance • san mateo ca

Last updated: 3 days ago

Senior Manager, Quality Assurance

GileadSan Mateo, CA, United States
$157,590.00–$203,940.00 yearly
Full-time

Senior Manager, Quality Assurance.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... Show more

Director, GMP Quality Assurance

Mirum PharmaceuticalsSan Mateo, CA, United States
$220,000.00–$240,000.00 yearly
Full-time

Director, GMP Quality Assurance.Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases.We are passionate about advancing scientific discoverie... Show more

AD/Director, Quality Assurance

AdeptsourceRedwood City, CA, United States
Full-time

AD/Director, Quality Assurance, Pharma.Type of role: FTE, Full time Salary: 181K - 214K plus bonus and equity.Develop and implement GXP including GMP quality systems in accordance with ICH, FDA, EM... Show more

Director, Quality Assurance Operations

Adicet BioRedwood City, CA, United States
$199,000.00–$274,000.00 yearly
Full-time

Director, Quality Assurance Operations.T cell therapies for autoimmune diseases and cancer.Adicet is advancing a pipeline of "off-the-shelf" gamma delta T cells, engineered with chimeric antigen re... Show more

Senior Manager, Clinical Quality Assurance

Corcept TherapeuticsRedwood City, CA, United States
$173,430.00 yearly
Full-time

Senior Manager, Clinical Quality Assurance.Redwood City, California, United States.For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that wh... Show more

Assoc Director, Quality Assurance GMP

ErascaSouth San Francisco, CA, United States
$175,000.00–$210,000.00 yearly
Full-time

Assoc Director, Quality Assurance GMP.South San Francisco, CA; San Diego, CA; remote.Erasca is a clinical-stage precision oncology company focused on discovering, developing and commercializing med... Show more

Quality Assurance Specialist

AIT Worldwide Logistics, Inc.South San Francisco, CA, United States
$74,840.00–$105,660.00 yearly
Full-time

The Quality Assurance Specialist is responsible for supporting and leading all quality management processes across the organization, applying specialized quality expertise at operational stations a... Show more

Quality Assurance Specialist

KellySouth San Francisco, California, US
$40.00–$42.00 hourly
Temporary

Kelly® Science & Clinical is seeking a Quality Assurance Specialist for a 6-month contract opportunity with one of our clients, a biotechnology company in South San Francisco that has pioneere... Show more

Training Supervisor, Quality Assurance

NateraSan Carlos, CA, United States
$106,200.00–$132,700.00 yearly
Full-time

Training Supervisor, Quality Assurance.The Training Supervisor, Quality Assurance is responsible for supporting training initiatives to drive operational efficiency and enhance workplace performanc... Show more

Director, Clinical Quality Assurance

CytokineticsSouth San Francisco, CA, United States
$222,480.00–$259,560.00 yearly
Full-time

Director, Clinical Quality Assurance.Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and ... Show more

Associate Director, Clinical Quality Assurance

Revolution MedicinesRedwood City, CA, United States
$186,000.00–$233,000.00 yearly
Full-time

Associate Director, Clinical Quality Assurance.Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patie... Show more

Director, Quality Assurance Compliance

Gilead SciencesSan Mateo, CA, United States
$210,375.00–$272,250.00 yearly
Full-time

Director, Global Supplier Quality Management Program.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... Show more

Executive Director Quality Assurance, External Manufacturing

VaxcyteSan Carlos, CA, United States
Full-time

Executive Director Quality Assurance, External Manufacturing.Join our Mission to Protect Humankind!.Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to prot... Show more

Quality Assurance Manager - GCP

Enigma SearchSouth San Francisco, CA, United States
Full-time

Quality Assurance Manager - GCP.South San Francisco, California, United States.About the Job Quality Assurance Manager - GCP.Our client is seeking a Senior Manager, Clinical Quality Assurance to pl... Show more

Senior Director, Quality Assurance

InsitroSouth San Francisco, CA, United States
$205,000.00–$218,000.00 yearly
Full-time

AI company dedicated to unlocking causal human biology and accelerating the delivery of better medicines to patients.Our unique Virtual Human platform identifies novel, high-impact genetic interven... Show more

Quality Engineer

Western MagneticsSouth San Francisco, CA, US
Full-time
Quick Apply

Westmag is the American manufacturer of drone motors and robot actuators, backed by Andreessen Horowitz, Founders Fund, Lux Capital, NFDG, Menlo Ventures, and other top investors.Westmag is committ... Show more

Work-From-Home Product Quality Assurance - $45 per hour

Great LionRedwood City, California
$45.00 hourly
Remote
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 more

 • Promoted

Director, Quality Assurance

ActalentSouth San Francisco, CA, United States
$80.00–$100.00 hourly
Full-time

Associate Director Of Quality Assurance.The Associate Director of Quality Assurance is responsible for the strategic development, leadership, and management of Quality Assurance operations supporti... Show more

Technical and Craft Labor - Quality Assurance Specialist

MindlanceSouth San Francisco, CA, United States
Full-time

Provide quality oversight for processes and projects, perform compliance assessments, develop the use of AI within Quality, perform internal audits, and ensure compliance to current regulations.A d... Show more

Director, Clinical Quality Assurance (CQA)

Coherus OncologyRedwood City, CA, United States
$190,000.00–$240,000.00 yearly
Full-time

Director, Clinical Quality Assurance (CQA).Title: Director, Clinical Quality Assurance (CQA).Reports to: Chief Medical Officer.Overview: The Director, Clinical Quality Assurance (CQA) will be accou... Show more

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Senior Manager, Quality Assurance

Senior Manager, Quality Assurance

GileadSan Mateo, CA, United States
30+ days ago
Salary
$157,590.00–$203,940.00 yearly
Job type
  • Full-time
Job description

Senior Manager, Quality Assurance

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 fulfil their aspirations. Join Gilead and help create possible, together.

At Gilead our pursuit of a healthier world for all people has yielded a cure for hepatitis C, revolutionary improvements in HIV treatment and prevention as well as advancements in therapies for viral and inflammatory diseases and certain cancers.

We set and achieve bold ambitions in our fight against the world's most devastating diseases, united in our commitment to confronting the largest public health challenges of our day and improving the lives of patients for generations to come.

As a Senior Manager, Quality Assurance at Gilead you will report to the Associate Director, Quality Assurance within the PDM External Quality organization. This position is dedicated to managing and supporting the Gilead Global Quality Agreement Program.

This position will have high visibility throughout the PDM organization as the Global Process Owner (GPO) for Gilead's Global Quality Agreement Program and will collaborate with key internal partners & stakeholders to establish and maintain an effective Global Quality Agreement Program. This position will serve as the primary subject matter expert (SME) for matters related to Quality Agreement content, Quality Agreement lifecycle management, Quality Agreement negotiations, management of Quality Agreement templates in compliance with applicable laws and regulatory requirements, and supporting continuous improvement initiatives related to the Global Quality Agreement Program.

Job Responsibilities

  • Serves as the Global Process Owner (GPO) for Gilead's Global Quality Agreement Program, ensuring the program is compliant, consistent, and effectively implemented across the organization
  • Develops, maintains, and continuously improves standardized Quality Agreement templates, guidance documents, training materials, and related tools to align with global regulatory requirements and internal policies
  • Serves as the primary subject matter expert (SME) for Quality Agreement content, interpretation, and applicability across internal teams and external partners, which may include supporting internal stakeholders during review, negotiation, implementation, enforcement, and periodic review of Quality Agreements.
  • Drives alignment and resolution of complex Quality Agreement terms through collaboration with Legal, Sourcing, and External Quality stakeholders
  • Establishes and maintains governance processes, metrics, and reporting for the Global Quality Agreement Program to ensure transparency and effectiveness
  • Monitors regulatory trends and evolving expectations related to Quality Agreements and proactively updates program requirements and templates accordingly
  • Provides expert support during inspections and audits related to Quality Agreements, including preparation, defense, and remediation activities
  • Leads or contributes to continuous improvement initiatives to enhance Quality Agreement processes, reduce cycle times, and improve compliance and user experience
  • Supports training and knowledge-sharing activities to ensure consistent understanding and application of Quality Agreement requirements across the organization

The Best Candidate

  • Demonstrates expertise in Quality Agreements, including development, negotiation, lifecycle management, and governance in a global GMP environment
  • Demonstrates strong working knowledge of global regulatory requirements applicable to Quality Agreements (e.g., FDA, EMA, ICH) and ability to translate requirements into compliant contract content
  • Demonstrates strong technical writing skills with the ability to draft, review, and standardize Quality Agreement templates and supporting documentation
  • Demonstrates advanced stakeholder management, influencing, and negotiation skills across cross-functional and external partner environments
  • Demonstrates ability to manage and support complex, high-visibility programs with multiple concurrent deliverables and competing priorities
  • Demonstrates strong communication skills, including the ability to clearly articulate Quality Agreement expectations to internal stakeholders and external partners
  • Demonstrates the ability to learn quickly and operate effectively in a fast-paced, highly regulated environment

Requirements

  • 8+ years of relevant experience in a GMP environment related field and a BS or BA OR
  • 6+ years of relevant experience in a GMP environment related field and a MA/MS OR
  • 2+ years of relevant experience in a GMP environment related field and a PhD/PharmD

Preferred Knowledge

  • Experience working with and managing relationships with Contract Manufacturing Organizations (CMOs) and other external partners is preferred
  • Experience interacting with regulatory authorities and supporting inspections related to Quality Agreements or external quality oversight is beneficial and preferred
  • Experience managing global programs or serving as a Global Process Owner (GPO) is beneficial
  • Familiarity with digital tools or systems supporting document management, contract lifecycle management, or Quality Agreement tracking is beneficial
  • Experience and working knowledge with digital Quality Management Systems and Quality Document Management Systems, particularly Veeva Vault, is beneficial.

People Leader Accountabilities

  • Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams.
  • Develop Talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose.
  • Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives, and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.

The salary range for this position is: $157,590.00 - $203,940.00. 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*.

* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.