Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

QA Specialist II

$102.09k - $132.11k

Gilead

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.Job DescriptionSpecific Job Responsibilities:Supports QA oversight of clinical small molecule drug substance and oral solid dosage (OSD) pilot plant manufacturing, warehouse, and is responsible for product disposition utilizing risk-based and clinical phase appropriate approach.Reviews and approves manufacturing documentation which may include batch records, product release documentation, deviations, investigations (i.e. OOS, OOT, atypical), CAPAs, change controls, protocols and reports.Maintains accurate, complete, and timely (ALCOA) quality records in accordance with GMP and quality systems.Supports QA team members in daily operations such as lot disposition and team process improvement projects.Participates in departmental and cross-functional projects, delivering assigned QA deliverables in compliance with quality systems.Supports small to moderately complex process improvement projects.Executes basic root cause analysis and uses risk-based thinking to support investigations and quality events.Helps identify data trends, anomalies, and potential compliance risks and escalates appropriately.Leads revision of GMP documentation to support QA projects.Creates metrics and reports under the supervision of senior QA team members.Supports regulatory inspections, internal audits, including preparation, execution, and observation response generation.Knowledge:Demonstrates working knowledge of current Good Manufacturing Practices (cGMPs).Demonstrates working knowledge of quality assurance systems, methods and procedures.Demonstrates knowledge of FDA / EMEA standards and quality systems.Demonstrates basic knowledge of six sigma, LEAN, and root cause analysis tools used for identifying and correcting causes of deviations.Demonstrates good verbal, written, and interpersonalcommunication skills.Demonstrates proficiency in Microsoft Office applications.Basic Qualifications:4+ years of relevant experience in a GMP environment related field and a BS.OR2 + years of relevant experience and a MS.Prior experience in pharmaceutical industry is preferred.The salary range for this position is: $102,085.00 - $132,110.00. 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: * Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.For jobs in the United States:Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact View email address on click.appcast.io for assistance.For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster.NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACTYOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACTGilead Sciences will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law.Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.For Current Gilead Employees and Contractors:Please apply via the Internal Career Opportunities portal in Workday.SummaryLocation: United States - California - Foster CityType: Full time

Vacancy posted 1 day ago
Similar jobs that could be interesting for youBased on the QA Specialist II in Foster, CA vacancy
  •  ...QA Specialist Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted... 
    Suggested
    Contract work

    Integrated Resources

    San Mateo, CA
    5 days ago
  • Guardant Health, Inc. is seeking a Clinical Laboratory Scientist II in Redwood City, CA to perform high-complexity testing (Next generation DNA sequencing), ensure quality control, report patient results, and maintain compliant records. The role requires a California CLS... 
    Suggested

    Guardant Health, Inc.

    Redwood City, CA
    4 days ago
  • $120k - $150k

     ...related field and/or equivalent experience and education.Minimum 5 years of Pharma/Biotech industry experience in Quality Assurance (QA) in a GxP environment.Experience in developing and implementing GxP quality systems to meet current regulatory and industry standards... 
    Suggested
    Full time
    Work at office
    Local area

    Revolution Medicines

    Redwood City, CA
    5 hours ago
  • A clinical-stage biotech company is seeking a Senior Specialist in Quality Assurance to oversee compliance and support quality investigation processes. The ideal candidate will have over 4 years of experience in a relevant role within the biotech sector and a Bachelor’... 
    Suggested

    Allakos

    Redwood City, CA
    5 days ago
  • AIT Worldwide Logistics is seeking a Quality Assurance Specialist to drive global quality management, ensure policy alignment, and support audits across locations. You will manage documentation, training dashboards, and KPI tracking to sustain a culture of safety and continuous... 
    Suggested
    Worldwide

    AIT Worldwide Logistics

    South San Francisco, CA
    2 days ago
  •  ...Senior Clinical Laboratory Scientist to perform high complexity molecular testing, including next generation sequencing, and uphold QC/QA standards. This on-site role requires meticulous records and the ability to multi-task in a fast-paced environment. The position... 

    Guardant Health

    Redwood City, CA
    3 days ago
  • $74.84k - $105.66k

     ...Quality Assurance SpecialistThe Quality Assurance Specialist is responsible for supporting and leading all quality management processes across the organization, applying specialized quality expertise at operational stations and serving as a key liaison for global and... 
    Work experience placement
    Local area
    Worldwide
    Flexible hours

    AIT Worldwide Logistics

    South San Francisco, CA
    5 days ago
  • $85k - $105k

     ...Quality Assurance Specialist Menlo Park MyOme's mission is to provide clinically actionable genetic information to patients throughout...  ...and deadlines. What You'll Do: Support daily QA activities for clinical laboratory operations and help maintain... 
    Work at office

    MyOme

    Menlo Park, CA
    2 days ago
  • $32 - $34 per hour

     ...Quality Assurance Specialist - Biotech / Life Sciences Adecco Healthcare & Life Sciences is hiring for a leading global life sciences organization known for developing innovative technologies and solutions supporting genetic science, molecular biology, and next-generation... 
    Hourly pay
    Weekly pay
    Contract work
    Temporary work
    Local area
    Monday to Friday

    Adecco US, Inc.

    South San Francisco, CA
    1 day ago
  • $41.47 - $62.21 per hour

     ...high level of individual responsibility and accountability and possess the ability to perform to the requirements listed below. The QA Associate must be comfortable in a rapidly evolving Biotech start-up environment. This is a part-time role with an expected schedule... 
    Hourly pay
    Part time
    Work at office
    Local area
    Flexible hours

    Karius, Inc.

    Redwood City, CA
    4 days ago
  • Karius in Redwood City, CA, seeks a Part-time Quality Assurance Associate to support the internal quality framework, document control, audits, CAPAs, deviations, and related activities. The role is approximately 28 hours per week in a fast-paced biotech startup. You will...
    Part time

    Karius, Inc.

    Redwood City, CA
    4 days ago
  •  ...Quality Systems Specialist III Performs a wide variety of activities to ensure compliance with applicable regulatory requirements. Participates in developing standard operating procedures to ensure quality. Maintains programs and processes to ensure high quality products... 

    Netpace

    San Mateo, CA
    2 days ago
  • $55k - $65k

     ...functionality, regressions, and overall stability Manually verify interactions between the app and hardware TMS device Execute full QA passes on daily builds across platforms Write clear, detailed, and reproducible bug reports Re-test resolved issues and confirm... 
    Full time
    Part time

    AMPA

    Palo Alto, CA
    3 days ago
  • Karius is seeking a part-time Quality Assurance Associate in Redwood City, CA to support the internal quality framework, audits, CAPAs, deviations, and training. This role requires strong writing, organization, and collaboration across teams in a rapidly evolving biotech...
    Hourly pay
    Part time

    Kariusdx

    Redwood City, CA
    5 days ago
  •  ...through industry-leading brands. Position: Quality Assurance Specialist Location: South San Francisco,CA 94080 Duration:...  ..., site procedures, and ISO 9001 requirements. Provides QA support for product development, product transfer, and post-market... 
    Temporary work
    Worldwide
    Monday to Friday
    Flexible hours
    Shift work

    TekWissen LLC

    South San Francisco, CA
    1 day ago
  • $55 - $60 per hour

     ...Quality Systems Specialist As a Quality Systems Specialist, you will support the PDM and Quality organizations by assessing training impact, designing risk-based and compliant training solutions, and optimizing training curricula aligned with job roles and Quality... 
    Contract work
    Temporary work

    Actalent

    San Mateo, CA
    2 days ago
  • $65k - $85k

     ...for functionality, regressions, and overall stabilityManually verify interactions between the app and hardware TMS deviceExecute full QA passes on daily builds across platformsWrite clear, detailed, and reproducible bug reportsRe-test resolved issues and confirm... 
    Full time

    Ampa

    Palo Alto, CA
    5 days ago
  • $45 - $65 per hour

     ...Job Description Job Description Job Title: Quality Systems Specialist Job Description The Quality Systems Specialist manages and optimizes change control processes across manufacturing products, processes, equipment, facilities, and computerized systems to support... 
    Contract work
    Temporary work
    Local area

    Actalent

    San Mateo, CA
    1 day ago
  • $55 - $60 per hour

     ...Job Description Job Description Job Title: Quality Systems Specialist Job Description As a Quality Systems Specialist, you will support the PDM and Quality organizations by assessing training impact, designing risk-based and compliant training solutions, and optimizing... 
    Contract work
    Temporary work

    Actalent

    San Mateo, CA
    1 day ago
  • $55 - $60 per hour

     ...Job Description Job Description Job Title: Quality Systems Specialist - Training Specialist As a Training Specialist, you will support PDM and Quality organizations by assessing training impact, designing risk-based and compliant training solutions, and optimizing... 
    Permanent employment
    Temporary work

    Actalent

    San Mateo, CA
    1 day ago
  • $114.7k - $212.9k

     ...just build a plant-you will build the future of medicine. The Opportunity We seek a highly impactful Principal Quality Compliance Specialist who possesses extensive experience in quality, compliance, and project execution, combined with a strong risk-based operational... 
    Local area
    Relocation package

    Roche

    South San Francisco, CA
    3 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to QA Specialist II. Be the first to apply!