Review and support import documentation and entry activities, including alignment toHTS classification, valuation, origin, and FDA/CBER import requirements, while partnering with customs brokers and ...
Review and support import documentation and entry activities, including alignment toHTS classification, valuation, origin, and FDA/CBER import requirements, while partnering with customs brokers and ...
Director, Regulatory Affairs Advertising and Promotion
Foster City, CA · On-site
$174K - $230K/yr
Serves as regulatory liaison to FDA/CDER/OPDP or FDA/CBER/APLB for assigned products. * May lead local or global cross-functional process improvements or other special projects * Provides regulatory ...
Director, Regulatory Affairs Advertising and Promotion
Foster City, CA · On-site
$174K - $230K/yr
Serves as regulatory liaison to FDA/CDER/OPDP or FDA/CBER/APLB for assigned products. * May lead local or global cross-functional process improvements or other special projects * Provides regulatory ...
Serves as regulatory liaison to FDA/CDER/OPDP or FDA/CBER/APLB for assigned products. * May lead local or global cross-functional process improvements or other special projects * Provides regulatory ...
Serves as regulatory liaison to FDA/CDER/OPDP or FDA/CBER/APLB for assigned products. * May lead local or global cross-functional process improvements or other special projects * Provides regulatory ...
Director, Regulatory Affairs Advertising and Promotion
Foster City, CA · On-site
$174K - $230K/yr
Serves as regulatory liaison to FDA/CDER/OPDP or FDA/CBER/APLB for assigned products. * May lead local or global cross-functional process improvements or other special projects * Provides regulatory ...
Director, Regulatory Affairs Advertising and Promotion
Foster City, CA · On-site
$174K - $230K/yr
Serves as regulatory liaison to FDA/CDER/OPDP or FDA/CBER/APLB for assigned products. * May lead local or global cross-functional process improvements or other special projects * Provides regulatory ...
Senior Director, Regulatory Affairs
$259K - $317K/yr
Lead interactions with FDA (CDER/CBER/CDRH as applicable), EMA, and other global health authorities, including Type A/B/C meetings, Scientific Advice, and Innovation Office engagements * Partner with ...
Senior Director, Regulatory Affairs
$259K - $317K/yr
Lead interactions with FDA (CDER/CBER/CDRH as applicable), EMA, and other global health authorities, including Type A/B/C meetings, Scientific Advice, and Innovation Office engagements * Partner with ...
Senior Director, Regulatory Affairs
Newark, CA · On-site
$259K - $317K/yr
Lead interactions with FDA (CDER/CBER/CDRH as applicable), EMA, and other global health authorities, including Type A/B/C meetings, Scientific Advice, and Innovation Office engagements * Partner with ...
Senior Director, Regulatory Affairs
Newark, CA · On-site
$259K - $317K/yr
Lead interactions with FDA (CDER/CBER/CDRH as applicable), EMA, and other global health authorities, including Type A/B/C meetings, Scientific Advice, and Innovation Office engagements * Partner with ...
Senior Director, Regulatory Affairs
Newark, CA · On-site
$259K - $317K/yr
Lead interactions with FDA (CDER/CBER/CDRH as applicable), EMA, and other global health authorities, including Type A/B/C meetings, Scientific Advice, and Innovation Office engagements * Partner with ...
Senior Director, Regulatory Affairs
Newark, CA · On-site
$259K - $317K/yr
Lead interactions with FDA (CDER/CBER/CDRH as applicable), EMA, and other global health authorities, including Type A/B/C meetings, Scientific Advice, and Innovation Office engagements * Partner with ...
Lead interactions with FDA (CDER/CBER/CDRH as applicable), EMA, and other global health authorities, including Type A/B/C meetings, Scientific Advice, and Innovation Office engagements * Partner with ...
Quick apply
Lead interactions with FDA (CDER/CBER/CDRH as applicable), EMA, and other global health authorities, including Type A/B/C meetings, Scientific Advice, and Innovation Office engagements * Partner with ...
Senior Director, Regulatory Affairs
Newark, CA · On-site
$259K - $317K/yr
Lead interactions with FDA (CDER/CBER/CDRH as applicable), EMA, and other global health authorities, including Type A/B/C meetings, Scientific Advice, and Innovation Office engagements * Partner with ...
Senior Director, Regulatory Affairs
Newark, CA · On-site
$259K - $317K/yr
Lead interactions with FDA (CDER/CBER/CDRH as applicable), EMA, and other global health authorities, including Type A/B/C meetings, Scientific Advice, and Innovation Office engagements * Partner with ...
Quality Engineer 2
San Diego, CA · On-site
$80 - $125/hr
... CBER, and ISO regulations, including 21 CFR Part 820, ISO 13485, and ISO 14971, is required. * Working knowledge of 21 CFR Part 11 is required. * Must follow all applicable FDA regulations and ISO ...
Quality Engineer 2
San Diego, CA · On-site
$80 - $125/hr
... CBER, and ISO regulations, including 21 CFR Part 820, ISO 13485, and ISO 14971, is required. * Working knowledge of 21 CFR Part 11 is required. * Must follow all applicable FDA regulations and ISO ...
Quality Engineer 2
San Diego, CA · On-site
$79K - $124K/yr
... CBER, and ISO regulations, including 21 CFR Part 820, ISO 13485, and ISO 14971, is required. * Working knowledge of 21 CFR Part 11 is required. * Must follow all applicable FDA regulations and ISO ...
Quality Engineer 2
San Diego, CA · On-site
$79K - $124K/yr
... CBER, and ISO regulations, including 21 CFR Part 820, ISO 13485, and ISO 14971, is required. * Working knowledge of 21 CFR Part 11 is required. * Must follow all applicable FDA regulations and ISO ...
Quality Engineer 2
San Diego, CA · On-site
$79K - $124K/yr
... CBER, and ISO regulations, including 21 CFR Part 820, ISO 13485, and ISO 14971, is required. * Working knowledge of 21 CFR Part 11 is required. * Must follow all applicable FDA regulations and ISO ...
Quality Engineer 2
San Diego, CA · On-site
$79K - $124K/yr
... CBER, and ISO regulations, including 21 CFR Part 820, ISO 13485, and ISO 14971, is required. * Working knowledge of 21 CFR Part 11 is required. * Must follow all applicable FDA regulations and ISO ...
(RN) TIL Therapy Nurse Coordinator - 141125
San Diego, CA · On-site
$69.97 - $98.01/hr
Food and Drug Administration (FDA) Center for Biologics Evaluation and Research (CBER), and The Joint Commission. Autonomous nursing care is the ability of a nurse to assess and provide nursing ...
New
(RN) TIL Therapy Nurse Coordinator - 141125
San Diego, CA · On-site
$69.97 - $98.01/hr
Food and Drug Administration (FDA) Center for Biologics Evaluation and Research (CBER), and The Joint Commission. Autonomous nursing care is the ability of a nurse to assess and provide nursing ...
New
Fda Cber information
See California salary details
$13.52 - $18.61
2% of jobs
$18.61 - $23.70
1% of jobs
$23.70 - $28.79
2% of jobs
$28.79 - $33.88
3% of jobs
$33.88 - $38.97
5% of jobs
$38.97 - $44.06
11% of jobs
$44.30 is the 25th percentile. Wages below this are outliers.
$44.06 - $49.15
17% of jobs
The median wage is $51.43 / hr.
$49.15 - $54.24
20% of jobs
$54.24 - $59.33
11% of jobs
$60.51 is the 75th percentile. Wages above this are outliers.
$59.33 - $64.42
15% of jobs
$64.42 - $69.51
14% of jobs
$13
$51
$69
How much do fda cber jobs pay per hour?
What is an FDA CBER?
An FDA CBER job refers to a position within the Center for Biologics Evaluation and Research (CBER) at the U.S. Food and Drug Administration (FDA). CBER regulates biological products, including vaccines, blood products, and gene therapies, to ensure their safety and effectiveness. Employees in CBER roles may work in regulatory affairs, scientific research, policy development, or compliance oversight. These positions typically require expertise in biology, medicine, or regulatory science.
What are the typical daily responsibilities of someone working at FDA CBER?
Professionals at FDA CBER are usually involved in reviewing scientific data, assessing regulatory submissions for biologics, writing evaluation reports, and participating in team meetings to discuss product review findings. They commonly collaborate with scientists, physicians, and policy experts to ensure biologic products meet safety and efficacy standards. Day-to-day tasks may also include responding to inquiries from industry sponsors, developing policy guidance, and staying abreast of advances in biologic product development. This dynamic environment allows for constant learning and impact on public health through regulatory science.
What are the key skills and qualifications needed to thrive in the FDA CBER position, and why are they important?
To thrive at FDA CBER (Center for Biologics Evaluation and Research), you need expertise in biological sciences, regulatory affairs, and data analysis, often supported by an advanced degree in a relevant scientific field. Familiarity with regulatory databases, clinical trial management systems, and guidance documents such as CFR Title 21 is crucial. Strong analytical, communication, and teamwork skills help you effectively evaluate product safety and efficacy while coordinating with diverse stakeholders. These abilities ensure that biologic products are rigorously reviewed for safety, quality, and compliance with federal regulations.
How to become an FDA CBER investigator?
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For Fda Cber jobs in California, the most frequently searched job titles are:
What job categories do people searching Fda Cber jobs in California look for?
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Full-time
Medical, Dental, Vision, Retirement, PTO
Re-posted 7 days ago
AstraZeneca rating
8.4
Based on 45 frontline employees who took The Breakroom Quiz
24th of 86 rated pharmaceutical
Job description
AtAstraZeneca Cell Therapy, we are building the capabilities required to deliver complex, personalized therapies through a highly coordinated, patient-centered, and globally scalable supply chain. In cell therapy, every movement matters. The reliable and compliant flow of patient materials, critical manufacturing inputs, intermediates, and finished product is essential to protecting product integrity, supporting manufacturing continuity, and helping therapies reach patients on time.
TheSenior Specialist, Cell Therapy Trade Compliance - Free Trade Zone Operationsplays a critical role in that mission by leading Free Trade Zone (FTZ) operationsat AstraZeneca's cell therapy manufacturing sites. This role helps ensure materials can move compliantly, predictably, and with full traceability through import/export and FTZ processes, while maintaining strong inventory control, audit readiness, and alignment tovein-to-vein timelinesand manufacturing schedules.This is an opportunity to work at the intersection oftrade compliance, cell therapy logistics, and patient-centered operations, helping build the cross-border capabilities needed to support future growth and the next generation of personalized medicines.
You will be responsible for the day-to-day operation ofFTZ activitiesthat support the compliant movement and control of materials across the cell therapy network. You will work closely withManufacturing, Supply Chain, Logistics, Quality, brokers, and external partnersto ensure high execution quality, strong documentation practices, and reliable support for time-critical operations.
Lead FTZ operations and compliance: Manage FTZ execution in line with19 CFR Part 146 (Foreign Trade Zones), internal procedures, and site requirements, including admissions, status elections, zone-to-zone transfers, removals, exports, weekly entries, and annual reconciliation activities.
Support compliant material controls: Help ensure FTZ-compliant storage and movement ofpatient-specific materials and critical raw materials with strong attention to traceability, segregation, documentation accuracy, and operational control.
Maintain Inventory, control and audit-ready records: Operate and maintain accurate FTZ inventory records within approved systems, support cycle counts and reconciliations, and ensure documentation is complete and compliance, and manage access controls.
Coordinate import execution and broker activities: Review and support import documentation and entry activities, including alignment toHTS classification, valuation, origin, and FDA/CBER import requirements, while partnering with customs brokers and internal stakeholders to resolve issues quickly and compliantly.
Support outbound FTZ shipment execution: Coordinate outbound movements from the FTZ for intermediates and finished product, ensuring documentation, customs processes, and shipment controls are completed accurately and on time.
Partner cross-functionally to support patient and manufacturing timelines: Work closely withManufacturing, Quality, Supply Chain to align FTZ activities with batch release and patient schedules.
Track performance and identify improvement opportunities: Monitor KPIs such as inventory accuracy, admission cycle time, entry accuracy, customs holds, and exception trends, and support root cause analysis and corrective actions that improve reliability, compliance, and operational efficiency.
Maintain procedures and support training: Help develop and maintain SOPs, work instructions, and role-based training materials for FTZ and import/export processes, while supporting knowledge sharing and consistent execution across the network.
Essential Qualifications
Bachelor's degree inSupply Chain, International Business, Logistics, Life Sciences, or a related field.
5+ Years experience incustoms brokerage, import/export operations, trade compliance, or global logistics, including hands-on experience withFTZ or bonded operations.
Strong working knowledge ofFTZ operations, customs documentation, broker coordination, and import/export execution.
Familiarity with19 CFR Part 146,HTS classification,customs valuation, andFDA/CBER import requirements.
Experience working in aregulated environment; experience inbiopharma, advanced therapies, or temperature-controlled logisticsis preferred.
Experience maintaining accurate records, supporting audits or inspections, and working within controlled systems and documented procedures.
Attention to detail, ability to manage multiple priorities, and comfort working in a fast-paced and highly controlled operational environment.
Strong written and verbal communication skills, with the ability to work effectively across internal teams and external partners.
Proficiency inExceland familiarity withinventory systems, broker portals, or logistics/trade systems.
Experience supportingcell therapy, biologics, advanced therapies, or other highly controlled healthcare logisticsenvironments.
Familiarity withGDP, GMP, GxP, and documentation practices relevant to regulated logistics and trade operations.
Experience supportingtemperature-controlled, cryogenic, or time-sensitive material movements.
Experience with operational reporting, KPI tracking, and continuous improvement activities.
#CellTherapy
The annual base pay for this position ranges from $89K to $134K. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
19-Aug-2026Closing Date
06-Sep-2026Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
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About AstraZeneca
Sourced by ZipRecruiter
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.
Industry
Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing
Company size
10,000+ Employees
Headquarters location
Cambridge, Cambridgeshire, GB