JOIN US! Adicet Bio, Inc. is a clinical stage biotechnology company discovering and developing allogeneic gamma delta T cell therapies for autoimmune diseases and cancer. Adicet is advancing a pipeline of “off-the-shelf”…
Redwood City, California, United States · Remote Solely
$181k–$217k/yr
Senior
About Delinea: Delinea is a pioneer in securing human and machine identities through intelligent, centralized authorization, empowering organizations to seamlessly govern their interactions across the modern enterprise. …
Skills: Software engineering management, Agile methodology, .NET, C#, Distributed systems
About Array Labs Array Labs builds advanced radar systems to help humanity understand and respond to changes across the physical world. We’re launching a coordinated fleet of radar satellites to create a high-resolution …
Job Description California applicants: Please click here to review the Costco Applicant Privacy Notice. The jobs listed are examples of the typical kinds of positions that Costco may hire for when openings exist. The lis…
Job Description California applicants: Please click here to review the Costco Applicant Privacy Notice. The jobs listed are examples of the typical kinds of positions that Costco may hire for when openings exist. The lis…
Job Description California applicants: Please click here to review the Costco Applicant Privacy Notice. The jobs listed are examples of the typical kinds of positions that Costco may hire for when openings exist. The lis…
Skills: Hearing aid dispensing, Team leadership, Personnel management, Hearing evaluation, Ear impression taking
The Chan Zuckerberg Initiative was founded in 2015 by Priscilla Chan and Mark Zuckerberg to harness the power of technology to pursue some of society’s most ambitious goals — from curing or preventing all disease to tran…
Skills: Contract Negotiation, Legal Drafting, People Management, Risk Management, Commercial Law
Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress dive…
Skills: Research informatics, Data management, Assay informatics, Workflow automation, Data governance
For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments…
Skills: Analytical Development, Quality Control, GMP, Drug Substance Development, Drug Product Manufacturing
Celonis is the global leader in Process Intelligence and the pioneer of Process Mining technology. As one of the world’s fastest-growing enterprise SaaS companies, we are changemakers pushing the boundaries of what’s pos…
Skills: Enterprise Architecture, Data Architecture, Cloud Strategy, Agentic AI, Process Mining
The Director of Omnichannel Product Management owns the product strategy and roadmap for the systems that run Balsam’s retail core: financial systems, warehouse and inventory management, and order management. This is the…
Skills: Product Strategy, Roadmap Management, Omnichannel Retail, Order Management Systems, Warehouse Management Systems
Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress dive…
Skills: Global Privacy Strategy, Data Protection Governance, GDPR Compliance, HIPAA Compliance, CCPA/CPRA Compliance
The Chan Zuckerberg Initiative was founded in 2015 by Priscilla Chan and Mark Zuckerberg to harness the power of technology to pursue some of society’s most ambitious goals — from curing or preventing all disease to tran…
Skills: Social Media Strategy, Content Management, Analytics & Reporting, Editorial Calendar Management, Cross-functional Collaboration
SB Energy
Talent Acquisition Manager
Redwood City, California, United States · Hybrid
$140k–$165k/yr
Senior+$4.0B raised
Do you want to work with high-caliber professionals in a dynamic and growing company? Are you entrepreneurial, hard-working, and collegial? Join us at SB Energy, a leading infrastructure company backed by SoftBank Group …
Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress dive…
Skills: CRM ecosystems, Field enablement, Veeva, Salesforce, Global platform strategy
WHAT IS BOX? Box (NYSE:BOX) is the leader in Intelligent Content Management. Our platform enables organizations to fuel collaboration, manage the entire content lifecycle, secure critical content, and transform business …
Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress dive…
Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress dive…
Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress dive…
Redwood City, California, United States · Remote OK
$144k–$180k/yr
Senior+
About Delinea: Delinea is a pioneer in securing human and machine identities through intelligent, centralized authorization, empowering organizations to seamlessly govern their interactions across the modern enterprise. …
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
$199k–$274k/yr
Full-time
bachelor degree
Annual cash bonus, Long-term incentives, Equity, Employee stock purchase plan, 401k with roth, Company match
Posted 14d ago
~40 hrs/week
Responsibilities
The Director of QA Operations is responsible for building and leading the QA team to ensure cGxP compliance across clinical and commercial manufacturing activities. This role involves cross-functional collaboration to manage quality systems, regulatory submissions, and continuous improvement initiatives.
Requirements
The ideal candidate must have a Bachelor's degree in a scientific discipline and over 10 years of experience in the life sciences industry, including at least 6 years in Quality Assurance. Strong knowledge of cGMP regulations, FDA/EMA guidelines, and prior experience in direct management are required.
Full job description
JOIN US!
Adicet Bio, Inc. is a clinical stage biotechnology company discovering and developing allogeneic gamma delta 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 receptors (CARs), to facilitate durable activity in patients. For more information, please visit our website at https://www.adicetbio.com.
Director, Quality Assurance Operations
Adicet Bio is seeking an experienced and motivated Director, Quality Assurance Operations. The Director of QA Ops is responsible for building and leading the QA Operations team and establishing relationships with internal personnel and external consultants/contractors, as necessary to support QA activities and responsibilities. This position will work cross-functionally with other departments such as: Manufacturing, Facilities, QC, Supply Chain, IT, MSAT, Process Development, Regulatory, Program Management, etc.
The successful candidate must thrive in a fast-paced team environment, have excellent communication, planning and organizational skills, and be able to independently manage timelines to meet Adicet’s priorities and communicated goals. The successful candidate will have working experience and knowledge leading cGxP QA activities during clinical development and commercialization of drug candidates. The ideal candidate must have experience in providing QA support for regulatory submissions of quality-related sections. The candidate will be reporting to VP of Quality Assurance and is responsible for the strategic development and management of QA operations to support CMC operations and clinical activities in compliance with FDA, ICH, EMA regulations, guidances, industry standards, and company policies. This opportunity is located at our corporate headquarters in Redwood City, California.
Key responsibilities: • Ensure current Good Manufacturing Practices (cGMPs) compliance for clinical manufacturing of phase I/II/III investigational product, and compliance to 21 CFR Parts 210, 211, ICH Guidelines and EU GMPs as applicable. • Accountable for lot disposition activities including batch record review, in-process/release and stability testing review, oversight of quality events relating to GMP product, process, or facility, etc. Will lead by example to partner with cross functional groups to meet company objectives in compliance with applicable regulatory guidelines. • Review approval of development activities in preparation for GMP such as development studies/reports, engineering activities, etc. • Collaborates with cross functional teams and champions the Quality Risk Management Program. • Responsible for the phase appropriate validation program. • Serves as team leader in quality related discussions, investigations, risk assessments, change controls, etc. to resolve potential product quality issues and to ensure they are appropriately addressed and justified. • Partners with Facilities and functional SMEs to support equipment qualifications and lifecycle management. • Collaborates with Quality Systems to manage the cGxP training program for internal manufacturing related functions. • Represents the organization during third-party audits and inspections as required. • Provides technical expertise and guidance in conducting investigations in regard to quality deviations, laboratory investigations/change controls systems for tracking statuses, follow-up, and liaison with applicable department investigation writers to ensure their complete and timely resolution. • Provides oversight for the raw material program, including raw material QA release. • Develop and implement procedures, programs and policies that support quality assurance functions and assure cGxP compliance. • Supports regulatory submissions of quality related sections. • Be a champion for continuous improvement. Identifies and drives continuous improvement initiatives and monitors progress of deliverables. • Other duties as required.
Qualifications: • Bachelor’s Degree in scientific or relevant disciplines in life sciences. • 10+ years of experience within the life sciences industry, preferably biotechnology, pharmaceuticals, or other regulated therapeutic environment with 6+ years in a Quality Assurance role • 5+ years of direct management experience • Demonstrated mastery of cGMP regulations and quality systems • Thorough knowledge of applicable regulatory requirements (FDA CFR, EMA, ICH, ISO, any other global laws/regulations) • Experience with Health Authority Inspections • Proficiency with electronic management systems (such as LIMS, eQMS,) • Strong interpersonal and communication skills: written and oral. • Outstanding planning, organization, and multitasking skills. • Travel as required. • Prior cell therapy experience is a plus
Pay Range
$199,000—$274,000 USD
Adicet fosters a collaborative, high-performing environment by prioritizing in-person engagement. To enhance teamwork and communication, employees are required to be onsite at least three days per week (Tuesday–Thursday mandatory), with some roles requiring full-time onsite presence.
At Adicet, our people are our greatest focus. We believe that attracting and retaining the best and brightest is the key to achieving our mission to deliver best-in-class gamma delta T cell therapies for patients fighting autoimmune diseases and cancer.
We offer a competitive compensation package including base salary, annual cash bonus, long-term incentives (equity), Employee Stock Purchase Plan (ESPP) and a 401(k) with ROTH and a 4.5% Company match.
To ensure the wellness of our employees and their loved ones, we offer comprehensive health plans (medical, dental, vision, etc.), Flexible Health and Commuter Spending Accounts (FSA) and a company matched Health Savings Account (HSA). We also offer a life, AD&D, short and long-term disability insurance, and legal, pet, and various other voluntary insurance programs.
We also believe our greatest ideas come when we are refreshed and focused, and we offer generous paid time-off including 13 company holidays, paid end-of-year winter break, vacation, sick time, and paid parental leave.
Adicet is located in a state-of-the-art facility and works to create an incredible office experience with an onsite gym and various other fitness options, onsite parking with electric vehicle charging stations and free shuttle (Caltrain), company-subsidized lunches (delivered onsite daily) and fully stocked breakrooms.
Adicet is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.
Adicet Bio, Inc. (Nasdaq: ACET) is a clinical stage biotechnology company discovering and developing allogeneic gamma delta 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 receptors (CARs), to facilitate durable activity in patients. For more information, please visit our website at https://www.adicetbio.com.
Your safety as a job seeker matters to us. Please be cautious of fraudulent recruitment activity claiming to represent Adicet. All approved positions are accessible via the Adicet Careers page at https://www.adicetbio.com/careers/openings/
Offices: 1000 Bridge Pkwy, Redwood City, California 94065, US · 131 Dartmouth Street, 3rd Floor, Boston, MA 02116, US · 36F, Huaihai International Plaza, No. 1045, Huaihai Middle Road, Xuhui District, Shanghai, China 200031, CN
oncology and autoimmune diseasesHealth CareBiopharmaClinical TrialsBiotechnologyMedicalTherapeutics
How much do Management & Leadership jobs in Redwood City, CA pay?
Based on 356 listings with disclosed salaries, most management & leadership jobs in Redwood City, CA pay between $102k–$260k per year. Individual offers vary with seniority, company size, and specialization.
How many Management & Leadership jobs are open in Redwood City, CA right now?
There are currently 419 open management & leadership positions in Redwood City, CA listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Management & Leadership roles in Redwood City, CA?
Companies currently hiring include Revolution Medicine, Delinea, Corcept Therapeutics, C3 AI, Box, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Management & Leadership jobs in Redwood City, CA?
Yes — 225 of the 419 open management & leadership positions offer remote or hybrid work (44 remote, 181 hybrid).
How do I apply for Management & Leadership jobs in Redwood City, CA?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.