Associate Director, Quality & GxP Compliance
SonoThera
SonoThera is seeking an Associate Director of Quality in the San Francisco Bay Area to lead the design and implementation of a robust QMS, ensuring GLP, GMP, and GCP compliance across CROs. This senior role reports to the VP, Head of Regulatory and Quality in a fast-paced biotech environment. The ideal candidate has 10+ years in biotech, deep FDA/ICH knowledge, and proven CRO management experience, including building quality processes in early-stage development. #J-18808-Ljbffr SonoThera
- The Associate Director of Quality is responsible for managing quality assurance activities, providing strategic... ...System (QMS), and ensuring compliance with FDA, ICH, and other regulatory standards... ...individual ensures compliance with GxP regulations (GLP, GMP, GCP as...SuggestedFull time
- ...Associate Director, Quality Assurance ComplianceAt Gilead, we're creating a healthier world for all people... ...Director, Quality Assurance Compliance at Gilead you will have the following... ...inspection metrics dashboards) in a GxP?compliant and inspection?defensible manner...SuggestedWork at officeLocal areaRemote work
$171k - $223k
...meaningful therapeutics to patients. This role delivers strategic GCP quality oversight across Denali's clinical trial portfolio, anchoring... ...the clinical development lifecycle. It sets the standard for compliance and ethical conduct across study teams, site leadership, and...SuggestedRemote jobLocal area- ...possible, together.Job DescriptionAssociate Director, Global Supplier QualityPosition SummaryThe Associate Director, Global Supplier Quality serves as the global program owner... ...consistency, reliability, and regulatory compliance across business and quality systems.Metrics...SuggestedFull timeContract workFor contractorsLocal area
- ...outmatch disease. Position The Associate Director, Computer Systems Assurance... ...leader within the Nurix Quality Systems organization, responsible... ...hosted platforms to support GxP-regulated activities across... ...; assess systems for compliance and provide guidance to cross...Suggested
- ...is hiring a self-motivated, experienced and detail-oriented GxP and Regulatory QA Lead to join our fast-growing drug discovery... ...QA Lead will be responsible for overseeing and ensuring quality and compliance of company's clinical/non-clinical operations related to drug...Full timeWork at office
$80 - $100 per hour
...Position Summary The Associate Director of Quality Assurance is responsible for the strategic development... ...programs. This role ensures compliance with FDA, EMA, ICH, and other applicable... ...progressive Quality Assurance experience in GxP-regulated environments. Minimum 5...Contract workTemporary work$225k - $262.5k
...diseases of cardiac muscle dysfunction. The Director of Quality Systems will be responsible for the... ...system, document control, and GxP training groups. This role will provide... ...support business objectives, regulatory compliance, and inspection readiness. Responsibilities...Full time$130 per hour
...Pharmacovigilance / Drug Safety Reports To: Director or Senior Director, Safety Science 12... ...rare genetic diseases. The Associate Director of Safety Science is responsible... ...01(k) Get notified about new Director Quality Compliance jobs in Brisbane, CA . South San Francisco...Contract work- Nurix Therapeutics is seeking an Associate Director, Computer Systems Assurance (CSA) in Brisbane, CA to lead the GxP CSA program across Quality Systems, IT, Regulatory Affairs, and Clinical Operations. The role focuses on risk-based validation of SaaS and cloud-hosted...
- ...clinical and commercial milestones, we are seeking a Senior Director of Quality Systems and Compliance to shape and lead our quality and compliance strategy.... ...a culture of continuous improvement to support GxP activities across the organization. This leader will partner...Work at officeLocal areaRemote work2 days per week
$220k - $240k
...seriously.POSITION SUMMARYThe Director, GMP Quality Assurance is responsible... ...priorities, provides technical and compliance leadership, resolves... ...requirements. The Associate Director/Director is accountable... ...negotiate Quality Agreements with GxP vendors, intra-company...Contract workLocal area$170k - $200k
...inhibits ITK to modulate and control parallel signaling pathways in the immune system. Reporting to the Director of Analytical Development and Quality Control, the Associate Director of Analytical Development & Quality Control will serve as a key member of the CMC team,...Full timeWork at officeImmediate start$198k - $257k
Associate Director, Clinical Pharmacology & MIDD Full-time Zai Lab Limited(NASDAQ: ZLAB; HKEX: 9688) is an innovative, research... ...development questions. Ensure the scientific rigor, quality, and regulatory compliance of all clinical pharmacology and MIDD analyses and...Full timeWorldwideRelocation package- ...Senior Director, Quality As the Senior Director, Quality, you will serve... ...Operations. Quality Systems & Compliance: ·Own and continuously improve the company's GxP Quality Management System (... ...inspections, and manage all associated audit responses and CAPAs....
$210.38k - $272.25k
...DescriptionDirector, Global Supplier Quality Management ProgramPosition ImpactThe Director, Global Supplier Quality... ...of working, and enhances quality, compliance, supply continuity, and operational... ...industry-leading practices.Support SAP GxP Supplier process definition, data...Full timeFor contractorsLocal area$229.5k - $255.87k
...script to outmatch disease. Position The Associate Director, Pharmacovigilance Operations (PVO) is... ...for all PV operational and compliance aspects of assigned Nurix products across... ...assigned products, driving in-stream quality review, regulatory submission oversight...Temporary work$210k - $260k
Associate Director, CMC Project Management Full-time Department: Supply Chain & Program Mgmt... ...Clinical Development, Regulatory Affairs, Quality, Supply Chain, Commercial, and Finance... ...quality, timelines, or regulatory compliance. Partner with Finance to ensure transparency...Full time$300k - $350k
...decision making.Summary:The Executive Director, Quality Assurance, External Manufacturing is responsible... ...across the external network, ensuring compliance, supply continuity, and effective... ...QA leadership for externally executed GxP activities, including manufacturing and...Contract workRelocationRelocation package2 days per week3 days per week$260k - $275k
...using adenovirus and TLR3 agonists. We are looking for a Sr. Director, Quality Assurance (QA) to join our South San Francisco team. This is... ...CDMOs/contract laboratories to identify and elevate compliance risks, enable proactive decision‑making, and ensure product...Contract workFor contractorsWork at officeShift work$167k - $206k
...Position Summary IDEAYA is seeking an Associate Director, Supply Chain Operations to lead end-to... ..., maintaining strict regulatory compliance, and optimizing inventory. Strong Enterprise... ...real-time visibility and agility. Quality & Compliance: Partner with Quality and...Temporary workWork at officeLocal areaWork from home- ...Description Job Description Job Title: Associate Director, Bioanalytics Location: Thousand... ...Operations, Regulatory Affairs, and Quality teams to ensure delivery of high-... ...timely delivery of high-quality data and compliance with project timelines and budgets....
$273k - $290k
...inflection point.We are looking for a Senior Director of Quality Assurance to build a pragmatic,... ...with substantial outsourced execution.GXP Bridge: Deep expertise in either GMP or... ...subject to the terms of those plans and associated policies.In addition, insitro also provides...Home officeFlexible hours3 days per week- ...leading biotech company is seeking a self-motivated GxP and Regulatory QA Lead to oversee compliance within clinical and non-clinical operations. The role requires at least 7 years of relevant experience in Quality Assurance within the pharmaceutical or biotechnology...Full time
- Nurix Therapeutics is seeking an experienced Senior Director, Quality Control to join the Analytical Development and Quality Control group. This leader will establish and run a QC function, creating systems, infrastructure, and a team to support programs from CMC development...
- Associate Director, CMC Project Management About the job Associate Director, CMC Project Management... .... Working closely with CMC, Quality, Regulatory, Clinical Supply, and Program... ...programs is a plus. Familiarity with GMP/GxP environments and quality management systems...Work at office
$193.5k - $236.5k
...Join Maze Therapeutics as our Associate Director, CMC Project Management. In... ...partner closely with CMC, Quality, and key internal stakeholders... ...others to reinforce process compliance, what good looks like, and... ...plus. Familiarity with GMP/GxP-regulated environments and quality...Work at officeShift work$115k - $130k
...Job Title: Quality Control Manager | Food Manufacturing Job Description This hands-on Quality Control Manager role leads the... ...documentation. Conduct routine production floor audits to verify compliance with Good Manufacturing Practices (GMPs), food safety...Weekly payPermanent employmentContract workWork at officeAll shiftsMonday to FridayShift work- ...cleared for use in the US, UK, Europe, Japan and Canada, and has been used for more than 750,000 patients worldwide. The Director, Clinical Quality & Compliance is responsible for the strategic oversight, management, and execution of clinical quality assurance and regulatory...Work experience placementWork at officeLocal areaWorldwideRelocationShift work
$186k - $235k
...geographic location.Position Summary:The Associate Director of Medical Writing will be responsible for... ...programs, while also performing quality control (QC) reviews, document formatting, and editing to ensure compliance with regulatory standards, internal guidelines...Contract workRemote work
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