Today's Pharma & Biotech Jobs

A Senior Research Assistant will support preclinical studies at all stages conducted at Sarepta Therapeutics through internal procurement and the execution of cardiac, behavioral, and muscle-based functional outcomes to characterize rodent models and assist in testing drug efficacy. The Senior Research Assistant will need to multitask with a strong ability to communicate, stay organized, and document in accordance with GLP. Tasks will need to be performed in accordance with SOPs and per study specifications. The Senior Research Assistant will need to follow instructions and at times work independently. Additionally, the Senior Research Assistant will need to demonstrate proficiency in rodent...

The Associate Director, Labeling and Disclosures, will be responsible for leading global labeling activities for development and/or marketed products, and leading disclosure activities for applicable clinical trials. The Associate Director is responsible for the development, maintenance, and harmonization of core labeling (e.g., CCDS) and local labeling, ensuring compliance with applicable regulatory requirements while supporting business and lifecycle objectives. The Associate Director may also oversee the end-to-end operations for clinical trial registration, maintenance and results posting on Health Authority-managed databases worldwide (e.g., Clinicaltrials.gov, EudraCT). The Associate Director is responsible for effectively partnering and engaging with internal (e.g., cross-functional study teams, senior...

The Research Associate (RA) I/II, Early Stage Process Development, provides support to the Cell Line and Upstream Process Development in the execution of experiments for the development and optimization of upstream processes to produce siRNA and AAV vectors. This role utilizes their biochemistry, cell biology and engineering experience to generate reliable and reproducible data with thorough documentation to support early research and development, pre-clinical manufacturing and scale-up operations. The RA I/II is expected to work closely with Downstream Process Development, Analytical Development and Vector Core groups to foster collaborative environment that delivers sound and robust manufacturing processes. The Opportunity to...

The Marketing Manager efdoralprin Alfa will support the execution of the global HCP and patient marketing strategy for efdoralprin alfa (Dora) in Alpha-1 Antitrypsin Deficiency (AAT). This is a hands-on execution role for a high-potential marketer looking to build deep rare disease launch experience on a once-in-a-generation opportunity — the first meaningful innovation in AAT treatment in 30–40 years. AAT is a genetic disease-causing severe lung disease and premature death if left untreated, yet it remains chronically underdiagnosed. This role is critical to executing both HCP engagement and patient marketing initiatives before and through launch, translating strategy into flawless day-to-day...

Location Cambridge or East Hanover #LI-Hybrid 3 days/week in office Internal The Executive Director, Applied AI Lead Novartis is making a significant long-term investment in becoming an AI-first organization, with sponsorship at the highest levels of the company. This is a rare opportunity to shape how generative AI and agentic systems are engineered, deployed and adopted across a global enterprise whose work ultimately supports patients and healthcare systems worldwide. As Executive Director of Applied AI, you will combine technical depth, product thinking and enterprise influence to turn high-value business challenges into secure, scalable AI products and intelligent workflows. You...

The Senior Manager, Business Development Analytics role is a critical member of the Business Development and Strategy Analytics team. The Senior Manager serves as a key internal consultant to BMS’s leadership team by conducting financial analysis of business development opportunities and by providing valuation insights for deals, with the goal of enabling value-driven R&D & M&A decisions. They also act as integrators of other analytic services, helping development teams ensure that they make the most of BMS's full analytics capabilities. The ideal candidate will have a strong background in statistics, forecasting, decision analysis, risk assessment, as well as prior experience...

General/ The Senior Director, CGT Quality Systems, Personalized Medicine provides strategic Quality leadership for personalized medicine and advanced cell therapies across the patient journey. The role is accountable for advancing Quality oversight, governance, compliance, and continuous improvement while ensuring efficient, patient-centric process across the end to end patient journey. This highly cross-functional position requires strong matrix leadership and partnership with Global Quality and Manufacturing, MS&T, Regulatory, Commercial, and Supply Chain stakeholders. Success requires the ability to influence enterprise decisions, build strong partnerships, and drive alignment through executive presence and effective communication. The ability to balance long-term vision with flawless execution...

Are you ready to shape how we educate healthcare professionals and translate brand educational objectives into impact at scale? This role puts you at the center of how we plan, deliver, and continuously improve compliant speaker programs that help clinicians make informed decisions for their patients. You will be the strategic partner to customer-facing leaders across Sales, Marketing, Medical, and Market Access—designing future-ready processes and engagement models while ensuring today’s programs run smoothly. Working across technology, commercial operations, brand teams, and compliance, you will balance immediate delivery with building the next wave of capability for an evolving US portfolio. Can...

AstraZeneca is seeking an experienced principal process engineer for our cell therapy Global Manufacturing Science and Technology (MS&T) team. This position is responsible for the technical oversight of robust, compliant, and cost-effective end-to-end cell therapy manufacturing processes. Activities include leading technology transfer for pivotal clinical manufacturing, process performance monitoring, defining process validation strategy, driving implementation of continuous process improvements, and authoring validation and regulatory deliverables to enable commercialization and lifecycle management across a global network of AstraZeneca’s manufacturing sites. The position reports to the Associate Director, Global MS&T, is based in Gaithersburg, MD, and follows an onsite work model. The...

At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately providing employees with the opportunity to work across teams, functions and even the globe. Do you have expertise in, and curiosity for leading Medical Affairs teams in Oncology ? Apply your experience to changing the way cancer is treated at AstraZeneca , a company that follows the science and turns ideas into life changing medicines. Help to advance our incredible pipeline by applying expertise and accelerating our pathway to finding a cure. A dedicated Oncology Business Unit (OBU), this is the...

Are you ready to lead EGFR lung cancer marketing that accelerates impact for patients and strengthens our market leadership? Based in Gaithersburg, Maryland and reporting to the Marketing Operations Director, you will play a pivotal role in a high-performing franchise with a deep pipeline and bold ambitions. This is a chance to develop the strategy and execution for key launches, alongside other brands in our pipeline. You will build and deliver commercial launch plans, monitor business performance, and turn scientific insights into measurable market outcomes. Can you combine rigorous evidence with creative, Digital First tactics that scale across channels? You...

Are you ready to turn real-world evidence into decisions that change how people living with cancer are treated? Can you see yourself shaping global and US strategy so that the right evidence reaches physicians, payers and patients at the moments that matter? In this individual contributor role, you will join a high-performing asset team that fuses science with strategy to generate and communicate compelling health outcomes evidence. Your work will connect ground breaking research with real clinical practice—advancing our pipeline, informing access, and improving the patient experience across the entire journey from diagnosis to survivorship. You will partner across Medical,...

AstraZeneca is seeking an experienced senior process engineer for our cell therapy Global Manufacturing Science and Technology (MS&T) team. This position is responsible for supporting the technical oversight of robust, compliant, and cost-effective end-to-end cell therapy manufacturing processes. Activities include leading technology transfer for pivotal clinical manufacturing, process performance monitoring, supporting definition of process validation strategy, leading implementation of continuous process improvements, and contributing to validation and regulatory deliverables to enable commercialization and lifecycle management across a global network of AstraZeneca’s manufacturing sites. The position reports to the Associate Director, Global MS&T, and requires up to 10% domestic and international...

Job Summary The Engineer – Facilities & Engineering is responsible for various technical aspects of facilities maintenance, validation activities, engineering projects, and mid-size capital investments within a pharmaceutical organization. This role involves providing technical input, overseeing facility and engineering related projects, and ensuring that all systems and processes meet regulatory requirements and support operational efficiency. Key Responsibilities Lead cross-functional teams supporting facilities maintenance, validation, metrology, engineering solutions, and capital projects. Oversee facilities operations across labs, manufacturing, and GMP spaces, driving improvements while ensuring health, safety, environmental, and regulatory compliance. Lead validation strategies, protocols, and documentation for systems and equipment, ensuring...

Job Summary The Engineer – Facilities & Engineering is responsible for various technical aspects of facilities maintenance, validation activities, engineering projects, and mid-size capital investments within a pharmaceutical organization. This role involves providing technical input, overseeing facility and engineering related projects, and ensuring that all systems and processes meet regulatory requirements and support operational efficiency. Key Responsibilities Lead cross-functional teams supporting facilities maintenance, validation, metrology, engineering solutions, and capital projects. Oversee facilities operations across labs, manufacturing, and GMP spaces, driving improvements while ensuring health, safety, environmental, and regulatory compliance. Lead validation strategies, protocols, and documentation for systems and equipment, ensuring...

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly,...