Senior Specialist, Cell Therapy Trade Compliance
$89k - $134kAstraZeneca
In AstraZeneca's Cell Therapy division, we follow the science to explore and innovate. We are working towards treating, preventing, modifying, and even curing some of the world's most complex diseases. We have the potential to grow our pipeline and positively impact the lives of patients around the world. We are committed to making a difference and have built our business around our passion for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs. Key Responsibilities FTZ operations and compliance: Operate per 19 CFR Part 146 and AZ SOPs; manage admissions (CBPF 214), status elections (NPF/PF), zone-to-zone transfers, removals/exports, weekly entries, and annual reconciliation; support CBP/FDA/CBER reviews and close CAPAs. Cell therapy material controls: Manage patient-specific inputs (apheresis, vectors, critical reagents) and cryogenic materials; ensure chain of identity/chain of custody, segregation, traceability, and cold/cryogenic storage integrity within the FTZ. Inventory, systems, and security: Maintain validated FTZ inventory records (ICRS/WMS) at lot/serial level; perform cycle counts and reconciliations; manage access controls/CCTV and documentation. Import governance: Oversee HTS classification, valuation, origin, and PGA requirements; ensure FDA/CBER admissibility and correct entry data; review/approve broker entry packages (3461/7501) and run broker scorecards/KPIs. Outbound from FTZ: Govern zone-to-export/domestic shipments for intermediates and finished product; ensure AES/EEI filings, license checks, temperature control, and documentation integrity. Cross-functional alignment: Coordinate FTZ/import timelines with Manufacturing/Tech Ops, QA/QC, Supply Chain, and Logistics to meet GMP batch release and patient schedules. Reporting and improvement: Track and report KPIs (admission cycle time, inventory accuracy, entry error rate, CBP/FDA holds, duty deferral/avoidance); lead root cause/Corrective Actions and drive process improvements. SOPs and training: Maintain FTZ/import SOPs and role-based training; coach site teams on FTZ procedures and documentation standards. Qualifications Bachelor’s in Supply Chain, International Business, Life Sciences, or related. 5+ years in customs brokerage, import/export, or trade compliance with hands‑on FTZ/bonded operations; biopharma/advanced therapies and temperature‑controlled logistics preferred. Working knowledge of 19 CFR Part 146, HTS classification, customs valuation, FDA/CBER import requirements. Proficiency with FTZ inventory systems, broker portals and use of MS Excel. Familiarity with GDP/GxP documentation and audit support. Effective communication and stakeholder management. Core Competencies Patient focus and integrity: Protects COI/COC, data integrity, and product quality in all FTZ activities supporting patient timelines. Deliver results: Executes admissions/entries/exports accurately and on time; sustains audit‑ready records and high inventory accuracy. Problem solving and judgment: Anticipates risks, resolves FTZ/import exceptions, and escalates appropriately. Collaborate and influence: Aligns brokers, internal teams, and carriers without direct authority to meet compliance and schedule needs. Data and digital: Ensures clean, timely system transactions; uses KPIs to drive corrective actions and continuous improvement. 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. Our 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. #J-18808-Ljbffr AstraZeneca
$89k - $134k
...At AstraZeneca Cell Therapy , we are building the capabilities required to deliver complex, personalized therapies... ...helping therapies reach patients on time. The Senior Specialist, Cell Therapy Trade Compliance – Free Trade Zone Operations plays a critical role in...SeniorTemporary work- ...seeking a dedicated professional for their Cell Therapy division in Los Angeles. This role focuses on managing FTZ operations and compliance, ensuring the integrity of patient-... ...have over 5 years in customs brokerage or trade compliance along with a Bachelor’s degree...Senior
$185k - $278k
AstraZeneca GmbH is seeking a Facilities Engineer in Los Angeles, California to establish design standards and ensure compliance for cell therapy manufacturing. You will evaluate network expansion opportunities and lead risk assessments for existing and new facilities....Senior$142.38k - $213.57k
...Principal Process Engineer for its Manufacturing Sciences & Technology team to support cell therapy production. This role involves managing engineers and overseeing manufacturing compliance while providing day-to-day support at the Santa Monica and Tarzana locations. Key...Suggested- ...Senior Therapeutic Area Specialist, Neuroscience Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually... ...optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients,...SeniorPrivate practiceWork at office
$139.23k - $168.71k
## Senior Therapeutic Area Specialist - Cobenfy -West LA, CALos Angeles - CAFind out how well you match with this job**Working with Us** Challenging... ...a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and...SeniorHourly payFull timeTemporary workPart timeFor contractorsSummer workPrivate practiceLive inWork at officeLocal areaRemote workFlexible hoursShift work- ...facility that comprises a cGMP cell manufacturing facility... ...generation of cell and gene therapies. With world class expertise in... ...treat disease. The Biomedical Specialist participates on wet‑ and dry‑... ...may execute tasks requiring compliance with all Federal and State accrediting...
$37.72 - $38.5 per hour
A renowned research university in California is seeking a cGMP Quality Control Associate to ensure the quality of cell and gene therapy products. This role involves conducting analytical testing, maintaining compliant laboratory operations, and collaborating with cross-...Hourly pay$297k - $330k
OpenAI is looking for a Senior Counsel, Sanctions and Trade Compliance to manage its sanctions compliance program. This hybrid or remote role involves advising cross-functional teams, developing compliance strategies, and owning documentation for compliance processes....SeniorRemote job$100k - $130k
PPG is seeking a Trade Compliance Manager to handle export control regulations in a hybrid role based in locations such as Sylmar, CA or Atlanta, GA. Responsibilities include maintaining export compliance procedures, providing consultative guidance, and conducting internal...Senior- AstraZeneca GmbH in Tarzana is looking for a Sr. Specialist Quality Engineering to oversee Quality Risk Management and ensure compliance with cGMP standards. The role involves... ..., and support in quality processes for Cell Therapy operations. Ideal candidates will have extensive...Senior
$87.58k - $92k
...prestigious university in California is seeking a Quality Control Specialist to oversee quality assurance in a cGMP facility. You will... ...'s degree in biotechnology and substantial experience in cell therapy and quality control. This full-time position offers a salary...Full time$100k - $120k
Simpson Thacher & Bartlett LLP is seeking an Assistant Managing Clerk in Los Angeles to assist with court filings and procedural guidance. The ideal candidate will have at least six years of relevant experience and a strong understanding of civil procedure in New York and...Senior- ...experience : High School Diploma with at least 5 years of relevant cell therapy, pharmaceutical, biotech, or GMP manufacturing experience, or... ...overtime as the need arises by the manufacturing schedule Compliance expectations : Must follow all safety, contamination control,...Hourly payTemporary workShift workWeekend work
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The PENTA Building Group is seeking a Senior MEP Specialist to join our team in Los Angeles County and Orange County ! A PENTA Senior MEP Specialist... ...quality control. Set guidelines and procedures to verify compliance with design documents and building codes. Coordinate with...SeniorContract workWork experience placementFor subcontractorLocal area$297k - $330k
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Senior Specialist Legal Editor, Commercial & Law Department Role Summary: Practical Law US is looking for a Senior Specialist Legal Editor... ...& Law Department will: Develop commercial legal and compliance content that is of national and global significance to be published...SeniorContract workPrivate practiceLocal areaFlexible hours$124k - $335k
Specialty/Competency: Customs & International Trade Industry/Sector: Not Applicable Time... ...and guidance to clients on tax planning, compliance, and strategy. These individuals help... ...transformation to advance their business goals. As a Senior Manager, you lead large projects and...SeniorFull time- ...Job Description Job Description International Trade Senior Associate Attorney or Counsel Direct Counsel is seeking an International... ...advising multinational companies on complex customs, trade compliance, export controls, sanctions, and national security matters....SeniorWork at office
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The University of Southern California is seeking a Quality Control Specialist to manage quality assurance for biologics and drugs at its cGMP facility in Glendale, CA. The ideal candidate will have at least a Bachelor’s degree in biotechnology and 3 years of relevant experience...Fixed term contract$87.58k - $92k
The University of Southern California seeks an experienced Quality Control Specialist to support cGMP manufacturing at its Keck School of Medicine in Los Angeles. This role involves designing and improving quality control tests to ensure product safety and efficacy. Candidates...Fixed term contract- Csbiomfg is looking for a Biomedical Specialist to join the Cedars-Sinai Biomanufacturing Center in West Hollywood, California. The role... ...QC functions and complex laboratory tasks while ensuring compliance with cGMP and laboratory SOPs. Ideal candidates will have a Bachelor...
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...ethical, and evidence-informed mental health care. This role offers autonomy while ensuring adherence to compliance standards, focusing on delivering personalized therapy and maintaining strong client engagement. Key responsibilities include conducting assessments,...SeniorFull timeWork at officeFlexible hours
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