Job Description

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. We present the products across multiple formats, including liquid, lyophilized, vial, prefilled, and cartridge-based presentations. Focus is on the successful product integration into drug/device combination product. You will also allow the assessment of life cycle development opportunities, provide expertise in technology transfer and drug product engineering and technology development by internal and external partnerships. You will also ensure the development of portfolio projects in a phase-appropriate manner while managing the budget and your partners. You will be a member of the Injectable Drug Product Management team. It 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 other departments in PDCS, and with Alexion Operations, Clinical Development, Quality, and Regulatory organizations.

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 into drug/device combination products. Alexion enables the department to progress its diverse portfolio. This portfolio spans peptide, nucleic acid, protein-based modalities, as well as modalities for gene delivery. People present these modalities in multiple forms, including liquid and lyophilized dosage forms in vial, prefilled syringe, and cartridge-based presentations. Ensure tech transfer of Alexion's portfolio with specialized input on engineering solutions for equipment and processes. Review and develop drug product techology roadmap and manage important investments. Assist and mentor colleagues in a matrix team for efficient and successful drug product development and manufacturing in a phase appropriate manner. Partner with functions across Alexion to build the best strategies for developing products in Alexion's diverse portfolio. Provide subject matter expertise for preparing regulatory filings, regulatory interactions including inspections, audits and is accountable for the technical content of the relevant drug product sections of regulatory submissions. Work with the Head on the development on drug product development strategies within PDCS and with partners in Operations, Regulatory Affairs, and Commercial organizations. Devote considerable time and effort in developing colleagues and the requisite to achieve Alexion's growing R&D pipeline.

You Have:

Must have a BS or equivalent in Bio/Chemical Engineering, Pharmaceutical Sciences, Biochemistry, or related discipline with relevant experience You have number of years of drug product development experience in formulation and process development and technology transfer for mAbs, proteins, peptides. synthetics and genomic medicine products At least 8 years of experience of direct experience developing approaches to allow drug product development for early and late-stage programs through licensure. At least 5 years of experience managing a team of scientists and engineers at different levels (directly or in a matrix team) Ensuring their career growth. Must be proficient in current approaches for formulation and drug product process development, manufacturing processes and equipment, and applying these to developing efficient approaches to ensure product licensure. Knowledge of high concentration protein formulation development, aseptic processes, to provide vial, prefilled syringe, cartridge presentations as liquid and lyophilization dosage forms is important. Knowledge of current regulatory guidelines and cGMP requirements is necessary .

Benefits offered include:

A qualified retirement program [401(k) plan] Paid vacation, holidays, and paid leaves Health benefits including medical, prescription drug, dental, and vision coverage following the terms and conditions of the applicable plans.

Additional details 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 to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles).


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