Jobs / United States / Astrazeneca Pharmaceuticals Lp

Astrazeneca Pharmaceuticals Lp

Senior Scientist - Cell Therapy Product Characterization

US - Gaithersburg - MD Posted today

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Sponsorship verdict

Sponsorship possible

One solid signal, not two. Worth applying, and worth asking about sponsorship early.

  • Employer is on a government sponsor recordThe US Department of Labor certified 99 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first.
  • The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
  • No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area.
  • What Astrazeneca Pharmaceuticals Lp paid sponsored hires in similar roles12 certified filings for “Assoc.
  • Confirmed live todayWhen a source last listed this job as open.
Details and sources
Employer is on a government sponsor record
The US Department of Labor certified 99 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. Source: LCA disclosure data (US Department of Labor (OFLC)).
No salary bar for this route
H-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
What Astrazeneca Pharmaceuticals Lp paid sponsored hires in similar roles
12 certified filings for “Assoc. Princ. Scientist, Vector Engineering & Cell Line Dev.” (Molecular and Cellular Biologists) in MD: $103k–$158k, median $136k. Most were filed at wage level IV (33%) — 4 lottery entries, ≈61% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).

US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).

A verdict summarises public evidence. It is not legal advice and never a guarantee: the employer and the immigration authority decide. Sign in to factor in where you can already work.

About the role

Senior Scientist, Cell Therapy Product Characterization   Location: Gaithersburg, MD, US  Position Summary   We are seeking a highly independent Senior Scientist to provide technical leadership in product characterization and potency method development for cell therapy products. The successful candidate will combine expertise in cell therapy with strong experimental judgment and data automation capability to develop fit-for-purpose analytical methods, evaluate complex product datasets, and translate findings into clear scientific recommendations. This individual will proactively propose solutions, define experimental study design, and collaborate across teams from research, process development, manufacturing, quality, and regulatory functions to advance programs from preclinical development through clinical stages.  Key Responsibilities   • Lead the development and execution of potency methods used to characterize the function and mechanism of action of cell therapy products.  • Develop platform- and program-specific product characterization strategies and help define critical quality attributes of cell therapy products.  • Identify, evaluate, and implement new analytical technologies, techniques, and instruments to interrogate cell health, phenotype, and function.  • Integrate and interrogate process, product release, and product characterization data to identify trends, generate hypotheses, and recommend follow-up studies or actions.  • Develop automated data workflows, repositories, and dashboards to enable efficient visualization and exploration of complex product datasets.  • Partner with process development teams to link process parameters to product quality attributes and evaluate the impact of process changes on product quality.  • Serve as a product characterization and potency subject matter expert supporting investigations of out-of-specification or otherwise atypical clinical lots, including recommending additional characterization needed to assess product quality.  • Author method development reports, product characterization reports, SOPs, technical presentations, and sections of regulatory filings.  • Lead cross-functional technical discussions, communicate study outcomes, and provide clear, scientifically grounded recommendations to project teams and governance forums.  • Operate with a high degree of independence by anticipating scientific needs, defining next steps, resolving technical challenges, and driving work to completion with limited direction.  • Mentor junior scientists and contribute to a collaborative, safe, • and scientifically rigorous laboratory culture.  Education and Experience   • PhD in Cell Biology, Immunology, Biomedical Engineering, Biotechnology, Biological Sciences, or a related discipline with at least 1 year of relevant experience; or MS with at least 4 years of relevant experience; or BS with at least 6 years of relevant experience.  • Demonstrated scientific leadership, initiative, organization, and accountability, with the ability to manage multiple priorities, anticipate needs, propose solutions, and deliver results independently in a fast-paced development environment.  • Proven expertise in developing analytical methods used to characterize potency/function/MoA of cell therapy products (e.g., cytotoxicity, proliferation, cytokine secretion, target-dependent activation, serial killing).  • Experience with multicolor flow cytometry, including panel design, experimental execution, troubleshooting, and complex data analysis.  • Advanced knowledge of T-cell biology and genetic engineering technologies, including the ability to apply biological principles to cell therapy product characterization questions.  • Demonstrated ability to design experiments, analyze complex

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