You Will: Formulation and process development, product integration, and manufacturing of patient-centered, unique injectable drug products for Alexion's diverse portfolio from pre-clinical to successful licensure. Lead interface with Operations, CMC Project management, Clinical Development, Regulatory on life cycle management opportunities. Develop drug product delivery strategies through internal/external partnerships and product integration int...
The Executive Medical Director (EMD) role is generally assigned to be responsible for overseeing 2 or more programs, providing oversight/guidance/mentoring to the Medical Directors and Clinical Development Scientists on the teams, serving on cross-asset strategic teams (e.g., disease strategy team) and providing input to strategic decisions at the TA Strategy Team and Global Medicine Team meetings. Generally, the role may include managerial respo...
Executive Medical Director, Clinical Development, Hematology Location: Boston, MA or Barcelona Spain This is what you will do: General Description of the Role The Executive Medical Director (EMD) role is generally assigned to be responsible for overseeing 2 or more programs, providing oversight/guidance/mentoring to the Medical Directors and Clinical Development Scientists on the teams, serving on cross-asset strategic teams (e.g., disease strate...
We are looking for graduate students majoring in Epidemiology, Biostatistics, Public Health, Computer Science, Data Science, or a related field for a 12-week internship role within our Alexion - AstraZeneca Rare Disease division in Wilmington, DE from May 18 2026 to August 7 2026. Position Description: Assist with data cleaning and data management of various types of data, such as survey, registry and claims/EHR data Execute the statistical analy...
This is what you will do: The Associate Scientist IV reporting to the Head of Clinical QC will have a primary responsibility for clinical stability, inventory and gLIMS/Sample management for GMP activities (inclusive of the clinical reference programs and certificate generation) as well as responsibility performing assigned experimental tasks to support compendial testing of manufacturing processes (i.e., performing analytical/characterization me...
Position Summary The Senior Quality Auditor at Alexion Rare Disease Unit (ARDU) has key responsibilities for auditing a variety of GMP/GDP sites (internal and external suppliers) used for commercial and development projects. The manufacturing sites audited range from biotechnology, combination products, medical devices, raw material to fill finish facilities. Laboratory and distributor facilities are also audited. The auditor will assess the inte...
Are you ready to make a significant impact in the world of rare diseases. As the Associate Director of Strategic Planning & Execution for US Medical Affairs, you will drive strategic initiatives and collaborate with Therapeutic Area (TA) Leadership teams to align projects with our overarching goals. Your role will involve analyzing, resolving, and communicating key strategic programs, enabling informed decision-making that contributes to our succ...
We are looking for an undergraduate student majoring in finance, accounting, or a related field for a 10-week internship role at our Alexion: AstraZeneca Rare Disease site in Boston, MA from June 1 2026 to August 7 2026. Position Description: Learn the full GTN waterfall (list price to net sales), including accrual methodologies for rebates, chargebacks, Medicaid/340B, wholesaler fees, distribution/service fees, returns, and co-pay programs. Reco...
This is what you will do: The Senior Manufacturing Specialist is responsible for sustaining asset management programs and facilities program compliance to ensure manufacturing readiness, safety, and regulatory conformance. This role partners closely with Facilities, Quality, EHS, Operations, and external service providers to drive risk-based decisions, maintain audit readiness, and implement continuous improvements across equipment lifecycle and ...
This is what you will do: The Associate Director will lead the development, characterization, technology transfer, and validation of sterile injectable drug products across a range of modalities including biologics, peptides, nucleic acids, and synthetic molecules. This role spans early-phase development through commercialization and includes responsibility for liquid and lyophilized formulations in vials, prefilled syringes, and cartridges. The ...
This is what you will do: The Associate Scientist IV will join Injectable Drug Product Development group to support the formulation and drug product process development of Alexion’s biotherapeutic candidates. This individual will develop injectable formulations with fit for purpose analytical methods, perform analytical testing, and draft reports for the executed studies. This individual will work independently in a dynamic team environment and r...
This is what you will do: The Associate Director of Statistical Programming will be primarily responsible for overseeing statistical programming activities for multiple clinical studies, maintaining programming infrastructure and ensuring compliance with SOPs to produce quality and timely deliverables. He/she must possess extensive experience and proven skills in the use of SAS within a Statistical Programming environment and complete knowledge a...
