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 10 hours ago
Similar jobs that could be interesting for youBased on the QA Specialist II in Foster, CA vacancy
  •  ...wearable patch defibrillator designed for patients at temporary elevated risk of sudden cardiac arrest. We seek a Quality Systems Specialist II to guide cross-functional teams in CAPA, NCR, change control, and other quality initiatives while ensuring ISO 13485 and QMSR... 
    Suggested
    Temporary work

    Regulatory Jobs

    Redwood City, CA
    2 days ago
  • $87k - $100k

     ...Deerfield Healthcare, Cormorant Asset Management, and Invus Opportunities. SUMMARY OF ROLE: We are looking for a Quality Systems Specialist II with passion for creating devices that save lives. The Quality Systems Specialist II works closely with cross-functional teams... 
    Suggested
    Temporary work
    Local area
    Visa sponsorship
    Work visa
    Relocation package
    Flexible hours

    Regulatory Jobs

    Redwood City, CA
    2 days ago
  •  ...QA Documentation Specialist - I Processes IT controlled documents such as computer system procedures, forms, specifications and test documentation in the Electronic Document Management System (EDMS) following defined processes/procedures. Scans, verifies and archives... 
    Suggested
    Work at office

    Careers Integrated Resources Inc

    San Mateo, CA
    6 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
    3 days ago
  •  ...Corcept Therapeutics seeks a Quality Systems GxP Training Specialist II to support the company's GxP training program through learning management system administration, compliance monitoring, and cross-functional coordination. This hybrid role in Redwood City involves... 
    Suggested

    Corcept Therapeutics

    Redwood City, CA
    3 days ago
  • $88k - $105k

     ...medical technology industries. What is the role? The Quality Specialist supports Quality Operations through the Quality Oversight of...  ..., and coordinate timely corrections with Manufacturing, QC, and QA. Ensure identified Quality Events, Deviations, OOS results, and... 
    Contract work
    Temporary work

    Aerogen

    Foster, CA
    3 days ago
  • TekWissen Group seeks a Quality Assurance Specialist for a 12-month onsite assignment in South San Francisco, CA. The role focuses on quality oversight, regulatory compliance, ISO 9001, internal audits, CAPAs, and continuous improvement across consumable, hardware, and... 
    Temporary work

    TekWissen LLC

    South San Francisco, CA
    2 days ago
  •  ...current product portfolio includes biolayer interferometry (BLI) systems using optic fiber biosensors. We are looking for a QA Specialist to join our Quality Assurance team. The QA Specialist will play an important role in maintaining the company’s established Quality... 

    Gator Bio

    Palo Alto, CA
    11 days ago
  •  ...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

    Redwood City, CA
    18 days ago
  • $115k - $135k

     ...Labcorp seeks a Computer Systems Validation Specialist for its Monogram Biosciences lab in South San Francisco. The role involves managing validation activities, designing test protocols, and performing equipment qualification across laboratory systems in a regulated... 
    Full time

    Labcorp

    South San Francisco, CA
    3 days ago
  •  ...improve quality of care, optimize clinical performance, and mentor staff across operations. The role partners with Clinical Managers, QA, Operations, Schedulers, and Intake to align patient outcomes with standards. Ideal candidates have strong clinical and data-driven... 

    AlphaCare Home Health Corp

    San Bruno, CA
    3 days ago
  •  ...Quality Systems Specialist The Quality Systems Specialist is responsible for supporting the development, implementation, maintenance, and continuous improvement of the company's Quality Management System (QMS) in alignment with business requirements and ISO 9001:20... 
    Work at office

    Delta Star

    San Carlos, CA
    4 days ago
  •  ...Quality Systems Specialist The resource should have 2-3 years of prior experience in a regulated cGMP environment. Prior experience...  ...responsibilities are: 1. Development and generation of weekly/monthly QA group metrics. The metrics tracked will be validation document... 

    Integrated Resources

    San Mateo, CA
    3 days ago
  • $140.4k - $163.8k

     ...Cytokinetics seeks a Senior Quality Assurance Specialist for Drug Substance to provide GMP oversight of contract manufacturing operations and review batch documentation for clinical and commercial pharmaceutical products. The role supports quality compliance, regulatory... 
    Contract work

    Cytokinetics

    South San Francisco, CA
    13 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
    3 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
    2 days ago
  •  ...industry-leading brands. Position Details Position: Quality Assurance Specialist Location: South San Francisco,CA 94080 Duration: 12 Months...  ..., 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
    2 days ago
  • Job-ID: 201351Category: ResearchLocation: Stanford, CA, United StatesWorkplace: HybridContract: RegularPosted: 2026-10-09Pay Range: $77,971-$145,546Pay Frequency: AnnuallyFixed Term: NStanford Schools and Units: School of MedicineFull time or Part time: Full TimeClinical...
    Part time
    Work experience placement
    Work at office
    Local area
    Remote work

    Stanford University

    Palo Alto, CA
    9 hours ago
  • $115k - $135k

     ...lives. Labcorp is seeking a Computer Systems Validation (CSV) Specialist  to join our Monogram Biosciences lab in South San Francisco!...  ...instrument Maintenance of other Quality functions as designated by QA management Minimum Qualifications: ~ Bachelor’s degree in... 
    Full time
    Temporary work
    Casual work
    Internship
    Monday to Friday
    Flexible hours

    Covance Inc.

    South San Francisco, CA
    7 days ago
  • The Senior Quality Specialist is responsible for ensuring the effective execution of core Quality Management System (QMS) processes, including Document Control, Records Management, and Training, required for quality and manufacturing regulatory compliance. Principal... 
    Work at office

    Endovascular Engineering

    Menlo Park, CA
    2 days ago
  • Aechelon Technology, a Shield AI company, is a leading producer of 3D 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 helping...
    Contract work
    For subcontractor
    Trial period

    Jobleads-US

    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!