Jobs / United States / Astrazeneca Pharmaceuticals Lp
Director, Device Project Management
Astrazeneca Pharmaceuticals Lp · 🇺🇸 2 Locations
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 roles1 certified filing for “Associate Director, Oncology Portfolio Analytics” (Management Analysts) in MD: $157k–$157k, median $157k. Most were filed at wage level II (100%) — 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
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
Summary of the group: The Device Project Management Group drives AstraZeneca device project delivery, supporting clinical studies and commercial launch for AstraZeneca’s parenteral combination products. Device Project managers plan, coordinate, and deliver combination of product activities in line with project requirements and timelines; plan and monitor resources and expenses for product development; and perform strategic planning for platform and novel processes. The group interfaces globally with the CMC team, Drug Product team, Operations, Quality, Regulatory, and all development functions. The Director of Device Project Management will lead a group of project managers. You will work collaboratively with the Device Team Leads to ensure project goals and milestones are achieved, as well as the CMC PMs to ensure that Device activities align with the overall CMC Plans. You must effectively collaborate with staff and leaders in Device Development, Quality, Regulatory Affairs, Drug Development, Process Engineering and other areas of Biologics Product Development and AstraZeneca. Strong communication skills are required including succinct and effective presentation of technical and non-technical materials during meetings with company Senior Management / Leaders, health authorities, audits and other internal and external stakeholders. This role has high job complexity, and the successful candidate must have a high level of independence to meet the requirements outlined below with minimal to no supervision. Main Duties & Responsibilities: • Manages the Device Project Management group, including resource management, budget management, talent management, and employee development accountability • Responsible for ensuring Combination Product programs are delivered to time, quality, budget, project standards, company quality standards, and align with AstraZeneca’s strategy • Acts as a source of knowledge in area of expertise associated with defining, communicating and implementing device project management strategy as well as interpreting and applying Design Controls. Facilitates the planning, execution, and approval of Design Control Deliverables • Develops and maintains processes, tools, and technology required to effectively lead a portfolio of projects • Manages projects to ensure plans are optimal and meet overall strategic goals aligned with clinical and commercial development plans • Introducing new ways of leading and planning projects through use of available systems and resources • Leads and implements strategic initiatives related to Device Project Management and Combination Product Development Education & Experience Requirements: • Education: Bachelor's, Master's, or PhD in relevant technical disciplines such as Biomedical, Mechanical, or Chemical Engineering, or equivalent industry experience such as Device Development, Regulatory, Quality, or Process Engineering • Experience: 10+ years’ product development experience. 5+ years of Project Management experience (with the majority focused on Combination Product Development) • 3+ years of experience leading a project management office • Successful candidates must have experience in planning, managing, and executing functional and/or cross functional aspects of device development in the context of combination products and a working knowledge of biopharmaceutical product development • Experience managing distributed resources across multiple sites and time zones Education & Experience Requirements: • Education: Bachelor's, Master's, or PhD in relevant technical disciplines such as Biomedical, Mechanical, or Chemical Engineering, or equivalent industry experience such as Device Development, Regulatory, Quality, or Process Engineering • Experience: 10+ years’ produc