Jobs / United States / Astrazeneca Pharmaceuticals Lp

Senior Director, Cell Therapy Manufacturing Network F&E Lead

Astrazeneca Pharmaceuticals Lp · 🇺🇸 US - Rockville - MD

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. USCIS also records 31 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
  • 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. 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 roles15 certified filings for “Associate Director Oncology Outcomes Research” (Medical Scientists, Except Epidemiologists) in MD: $126k–$185k, median $140k. Most were filed at wage level II (47%) — 2 lottery entries, ≈31% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).
  • Confirmed live todayWhen a source last listed this job as open.

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.

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Sponsor Radar — Astrazeneca Pharmaceuticals Lp

99 H-1B filings certified since Oct 2025

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. USCIS also records 31 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).

Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Astrazeneca Pharmaceuticals Lp →

About the role

You will • Establish user requirements and facility design standards for cell therapy manufacturing ;   develop risk-based contamination control approaches that account for open and closed processing, personnel gowning regimes, environmental monitoring, and the unique biological risks inherent in patient-derived cellular materials   • Collaborate with Global Real Estate and Engineering to evaluate network expansion opportunities; provide cell therapy-specific input on site selection criteria, facility requirements, infrastructure needs, and operational considerations    • Provide input to and/or lead   e ngineering   s tudies   to inform capital investment decisions, site master planning,   new   technology   adoption   or platform changes     • Provide input to and   participate   in the established capital execution governance framework ,   planning   and reporting   • Lead identification and assessment of facility-related risks across existing sites and new-build programs ,   single points of failure in critical utilities, environmental control gaps,   safety   and infrastructure   risks   and develop mitigation   strategies that inform capital prioritization and operational decisions   • Harmonize F&E operating models across existing supply sites by   identifying   opportunities for standardization, shared processes, common resource models,   operating   costs   and aligned ways of working; develop a roadmap to bring consistency without disrupting ongoing operations   • Support development and deployment of Digital and AI solutions for Facilities & Engineering across the supply network   • Support implementation of   new technology   for existing F&E site teams—including training, resource planning, and adoption playbooks   • Support SHE management review based on data inputs from the supply sites;   identify   trends, compliance gaps, and improvement opportunities across the network;   • P rovide input to   cell therapy specific   sustainability initiatives aligned with corporate   strategy   You have • Education :   Bachelor’s degree in engineering   (Mechanical, Chemical, Civil/Structural, or Architectural Engineering);   Master's   degree preferred; professional engineering licensure (PE/CEng) desirable   • Experience : Minimum 10 years in pharmaceutical/biotech facilities engineering with at least 5 years in a network, multi-site, or above-site role; direct experience with cell   therapy, biologics, or ATMP manufacturing facility design strongly preferred; demonstrated experience developing user requirements and design standards for GMP facilities; involvement in greenfield or major expansion programs from conceptual design through operational handover   • Technical Knowledge : Expert knowledge of contamination control strategy for aseptic and cell therapy environments, cleanroom design (ISO classifications), pharmaceutical HVAC systems, GMP facility requirements, Engineering Studies, and commissioning/qualification protocols; familiarity with sustainability frameworks and current regulatory expectations for cell therapy facility design   • Skills : Engineering judgment, contamination control risk assessment, ability to develop standards and requirements, cross-functional collaboration, stakeholder influence across sites and the ability to translate manufacturing operational needs into facility design requirements; comfortable operating in a support and input role within matrixed governance structures    • Systems : Familiarity with BIM (Building Information Modeling), CMMS (Computerized Maintenance Management Systems), environmental monitoring systems, and energy management platforms. ​ The annual base pay for this position ranges from $185,000 to $278,000. Our positions offer eligibility for multiple in

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Source: Employer career site (Workday) First seen: 2026-10-01 Last confirmed: 2026-10-02 How our data works → Report this job

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