You will lead and direct the formulation and process development of patient-centered injectable drug products.These products are for Alexion's diverse portfolio, which spans synthetic, peptide, genomic medicine, and protein-based modalities in multiple formats, including liquid, lyophilized, vial, prefilled, and cartridge-based presentations. You will also lead life cycle development opportunities, provideexpertisein technology transfer and drug product engineering and technology development with internal and external partnerships. You will also ensure the development of portfolio projects in a phase-appropriate manner while managing the budget and interface partners. You will be a member of the Injectable Drug Product Management team and will need to collaborate and network with other departments within Product Development and Clinical Supplies (PDCS). Additionally, it will need to collaborate and network with Alexion Operations, Clinical Development, Quality, and Regulatory organizations.
Enablethe progression of Alexion'sdiverse portfoliothatspans peptide, nucleic acid, protein-based modalities, as well as modalities for gene deliveryasliquid and lyophilized dosage forms in vial, prefilled syringe, and cartridge-based presentations.
Provide subject matterexpertisefor preparing regulatory filings, regulatory interactions including inspections, audits and is accountable for the technical content of the relevant drug product sections of regulatory submissions.
Must have a BS or equivalent in Bio/Chemical Engineering, Pharmaceutical Sciences, Biochemistry, or related discipline with relevant experience
At least 8 years of experience in managing a group of drug product development scientists or engineers withendtoenddrug product developmentexperience(spanning formulation, process development, quality attribute assessment,techtransferand manufacturing support)formAbs,fusionproteins,injectablepeptides/syntheticsprograms.
Must be proficient in current approaches for formulation and drug product process development, manufacturing processes and equipment,regulatory expectationsand applying these to developing efficient approaches to ensure product licensure.
Knowledge of high concentration protein formulation development, aseptic processes, vial, prefilled syringe, cartridge presentations,liquid and lyophilization dosage forms is important.
Benefits offered include:
Health benefits including medical, prescription drug, dental, and vision coverage following the terms and conditions of the applicable plans.
Additionaldetails of participation in these benefit plans will be provided if an employee receives an offer of employment.The annual base salary for this position ranges from $175,000 to $263,000. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility toparticipatein our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles).
Date Posted
29-May-2026
Closing Date
29-Jun-2026
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.