Biologics Drug Product Development (Bio DPD), a part of Development Sciences within AbbVie’s R&D, is a global organization responsible for drug product formulation and process development, and definition of the product presentation for biologics (proteins, conjugates, peptides, neurotoxins etc.) and genetic medicine (AAV, LNPs, Cell Therapy).
Responsibilities
Provide strategic and technical oversight for drug product development of ultra-high concentration drug product formulation and process development and technology transfer, including fixed dose combinations for a wide range of biologics modalities.
Oversee drug product development of a portfolio of 5-7 pipeline programs spanning early- and late-stage development, including management of external partnerships as appropriate.
Effective and timely communication of development plans, risks, and mitigation plans to stakeholders and line management.
Initiate and/or sponsor scientific initiatives to drive innovation, continuously enhance capabilities and platforms, and improve business processes.
Accountable for the timely authoring of high-quality technical reports as well as drug product sections in global regulatory filings.
Requirements
BS in Pharmaceutics
MS in Pharmaceutical Sciences
PhD in Chemistry
PhD in Chemical Engineering
Nice to have: Ultra-high concentration liquid formulations for fixed dose combinations
Skills
Senior Group Director, Clinical Scientist - Immunology
Lead clinical science across AstraZeneca’s immunology portfolio, managing a team of scientists and driving clinical development strategy and execution.
Compensation
The annual base pay for this position ranges from $233,586.40 - $350,379.60 USD. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles.
The Clinical Nurse Consultant (CNC) is a trusted clinical expert responsible for developing professional relationships and educating key Health Care Professionals (HCP) involved in the care of patients receiving BMS hematology and oncology products in a defined geography.
Locations (2)
Cleveland, Ohio, United States
Columbus, Ohio, United States
Compensation
Field - United States - US: $142,710 - $172,927
Responsibilities
Drive peer to peer interactions with customers that optimize patient outcomes by delivering end-to-end clinical exchanges.
Deliver a continuum of clinical education and support to address the needs of HCPs.
Educate on unmet disease needs and discuss the current treatment landscape for hematology and oncology.
Develop and maintain relationships with academic and community HCPs within assigned geography to provide clinical and product education.
Actively assess the treatment and patient management landscape by meeting with HCPs to understand their needs and current patient management processes/protocols.
Comprehensive understanding of Legend and competitor products in our therapeutic area, and an in-depth knowledge of the complexities associated with the disease state
Ability to navigate a complex account environment and understand the needs/issues of various stakeholders at all levels within the account and triage to appropriate internal stakeholders for support.
Develops an understanding of the issues and opportunities unique to each geography.
Provides insights to the cross functional team on appropriate and timely feedback from interactions with healthcare professionals (HCPs), including account business trends and potential changes in therapeutic landscape.
Responsible for quality control activities for GMP manufacturing of cell and gene therapy products, including testing, sample management, equipment qualification, method development, data review, and audit participation.
Compensation
An applicant’s compensation package is finalized once the interview process is concluded and accounts for the nature of the role as well as the experience, competencies (job knowledge, skills and abilities) of the applicant and internal equity.
Responsibilities
Delivers quality control-related services including sample management, testing, method development, optimization, qualification and validation, stability program, data review and equipment management
Collaborates with Production, MSAT, and QA teams in preparation of master batch record, sampling plans, and specifications
Maintains the materials specification program
Releases materials
Manages the retain and references standard program
Requirements
Bachelor’s degree in science (bioengineering, chemical engineering, bioprocess, biotechnology, cell biology, microbiology, chemistry etc.)
Provide leadership and oversight for manufacturing operations within Cell Therapy while ensuring a safe, compliant, and efficient production environment.
Compensation
Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.
Responsibilities
Provide a safe, controlled work environment and ensure site safety objectives are communicated and understood by all manufacturing personnel.
Lead manufacturing teams and serve as the subject matter expert for assigned operations, including areas such as Cell Growth, Drug Product Filling, and related manufacturing processes.
Provide in-suite oversight during critical manufacturing activities such as harvest, vial filling, visual inspection, and other key production operations.
Support technical transfer activities, including process execution, methods transfer, engineering runs, training runs, water runs, and qualification activities.
Collaborate with Quality Assurance and cross-functional teams to establish procedures, quality systems, and manufacturing strategies for new and existing programs.
Requirements
Bachelor’s degree
Nice to have: automated drug product filling systems
Nice to have: RABS
Nice to have: isolator technology
Nice to have: automated or manual visual inspection systems
Lead manufacturing operations for the Swing Shift in a GMP cell therapy manufacturing environment, ensuring safe, compliant, and efficient execution.
Compensation
The annual base pay (or hourly rate of compensation) for this position ranges from $94,692.80 - 142,039.20. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles.
Responsibilities
Lead daily manufacturing operations for the assigned shift
Manage staffing, scheduling, and production readiness
Coordinate after‑hours support and escalation with cross‑functional teams
Serve as liaison with GMP facility cleaning and gowning vendors
Ensure compliance with cGMP, SOPs, batch records, and cleanroom standards
Lead global brand strategy and launch plan for cell therapy portfolio, driving commercial strategy across indications and markets.
Compensation
The annual base pay for this position ranges from $231,988 to $347,983. 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).
Responsibilities
Develop the global brand strategy and launch plan for Cell Therapy, including positioning, promotional strategy, and the go-to-market model.
Build the global capabilities, customer journeys, and treatment delivery models required to support launch readiness and execution.
Translate global strategy into clear implementation plans for regions and priority markets.
Partner across Medical, Market Access, Patient Affairs, Clinical, Regulatory, Analytics & Insights, Manufacturing, Supply, and country teams to align development and commercialization plans.
Integrate commercial insights—market opportunity, customer needs, competitive positioning, pricing, access, and treatment-delivery considerations—into development, regulatory, and portfolio decisions.
Requirements
Bachelor's degree in a relevant scientific discipline
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