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Celldex will make every effort to respond to inquiries from qualified applicants who have the skills and interests we are seeking. We will not be able to respond to recruiting and placement firms who contact us in an unsolicited manner, nor to unqualified applicants. Celldex is an equal opportunity employer dedicated to diversity in the workplace.
Individual is responsible for performing and understanding all tasks associated with Environmental Monitoring, Purified Water and raw material sampling and testing to support the Fall River Manufacturing facility.
The Associate Director, Quality Medical Device Engineer will lead quality oversight activities for drug-device combination products, including prefilled syringes, autoinjectors, on-body delivery systems, and related medical device constituents. This position will partner closely with Technical Operations, Device Development, Regulatory Affairs, Clinical, Supply Chain, and external manufacturing partners to establish and maintain compliant quality systems and ensure the successful development and commercialization of combination products.
The Talent Acquisition Partner (temporary) serves as a partner to hiring managers, providing consultative guidance across talent acquisition, workforce planning, and hiring execution. This role goes beyond traditional recruiting, advising leaders on how to attract, assess, and secure top talent aligned to Celldex’s growth, culture, and future commercial ambitions.
This individual will support hiring across Clinical, Quality, Medical Affairs, and Development functions, bringing deep market insight, proactive talent pipelining, and a data-driven approach to hiring decisions. The Talent Partner will play a critical...
The Vice President, Commercial Finance will build and lead Celldex’s Commercial Finance organization as the Company prepares for its first commercial launch and transitions from a clinical-stage biotechnology company to a fully integrated commercial biopharmaceutical organization.
Reporting to the Chief Financial Officer, the Vice President will serve as the senior Finance partner to Commercial leadership and will be responsible for the financial strategy, planning, forecasting, analytics and decision support required to successfully commercialize barzolvolimab and support future portfolio...
The Manager, Biologics Drug Substance External Manufacturing works cross-functionally with internal and external teams to support drug substance (DS) GMP external clinical and commercial manufacturing, oversee operations on-site at the Contract Development Manufacturing Organization (CDMO), support process technology transfer, process validation (PV), and continuous process verification (CPV) while adhering to Good Manufacturing Practices, company policies and procedures.
The Senior Manager Biologics Manufacturing Technical Support works cross-functionally with internal and external teams to lead technology transfer, provide manufacturing technical support, manage Contract Development Manufacturing Organization (CDMO) manufacturing deviations and investigations, process validation (PV), and continuous process verification (CPV) while adhering to Good Manufacturing Practices, company policies and procedures.
The Vice President, Corporate Controller will lead all accounting operations for Celldex, including corporate, R&D and commercial accounting, internal controls, financial close, technical accounting, revenue accounting, gross-to-net accounting, inventory and cost accounting, and related compliance activities.
As Celldex transitions from a development-stage biotechnology company to a fully integrated commercial organization, the Corporate Controller will play a critical leadership role in building a scalable, high-performing accounting organization...
The Sr. Director, HCP Marketing will lead the development and execution of the US HCP marketing strategy for barzolvolimab in preparation for Celldex’s first commercial launch. This role is responsible for defining the HCP journey, understanding key behavioral drivers, and building HCP engagement and activation strategies to deliver a highly successful launch.
Reporting directly into the Vice President of Marketing and Commercial Operations, this individual will work cross-functionally with Patient Marketing, Insights & Analytics, Sales, Market...
The incumbent will oversee and coordinate new projects related to validation deliverables and qualifications to ensure existing and new system installations meet all internal and external compliance requirements such as 21 CFR Part 11, EU GMP, and GLP requirements throughout the systems development life cycle. This position works on moderately complex problems of diverse scope where analysis of data requires solid evaluation of identifiable factors.
We are building a commercial insights platform that our field, brand, medical and market access teams will use to make decisions at launch and for years afterward.
You would be the first engineering hire on it. You will make the architectural decisions, stand up the infrastructure, build the backend and the services, and own how the whole thing is deployed, secured and released.
The Executive Director, Batch Release to lead the organization's commercial product disposition and batch release activities while ensuring compliance with global GMP regulations and quality standards. This leadership role will serve as the Quality representative responsible for final product disposition decisions, oversight of contract manufacturing organizations (CDMOs), and execution of quality systems supporting commercial manufacturing operations.
The Executive Director will...
This role will serve as the primary architect and leader of Celldex's inspection management program, ensuring continued state of readiness for regulatory authority inspections, partner audits, and commercial launch activities.
The Director will collaborate across Quality, Manufacturing, Supply Chain, Technical Operations, Regulatory Affairs, Clinical Development, and Commercial functions to establish and maintain a sustainable inspection readiness framework. The successful candidate will play a key role in supporting Celldex's transition from a clinical-stage organization to a...
The Quality Assurance Associate II performs documentation activities associated with manufacturing operations while ensuring compliance with GXP quality systems.
The Associate Director CMC Drug Substance works cross-functionally with internal and external teams to support drug substance (DS) GMP external clinical and commercial manufacturing, process technology transfer, process validation (PV), continuous process verification (CPV), preparing Module 3 of the CTD for commercialization of pipeline drug candidates while adhering to Good Manufacturing Practices, company policies and procedures.
The Executive Director, Quality CDMO Management at Celldex Therapeutics is responsible for providing strategic leadership and oversight of quality operations across the company’s external contract development and manufacturing organization (CDMO) network. This role ensures that all manufacturing, testing, and supply activities conducted by third-party partners comply with global GxP regulations, Celldex quality standards, and regulatory expectations. The Executive Director serves as a key cross-functional leader, driving quality risk management, audit readiness, vendor performance, and continuous improvement initiatives to support clinical and commercial development programs....
The Executive Director, Commercial Quality Systems is responsible for the strategic leadership, development, and continuous improvement of Celldex Therapeutics' Quality Management System (QMS) to support commercial and late-stage clinical products. This role ensures quality systems are compliant with global regulatory requirements, industry standards, and company objectives while fostering a culture of quality and operational excellence. The Executive Director oversees key quality processes, including deviations, CAPA, change control, complaint management, document control, training, and inspection readiness programs. As a senior...
Celldex is pioneering new horizons in immunology to deliver life-changing therapies. We are relentless in our pursuit of novel antibody-based treatments that engage the human immune system and directly affect critical pathways to improve the lives of patients with allergic, inflammatory and autoimmune disorders. We have built a culture where innovative and talented people thrive—focusing a significant effort on attracting and retaining passionate and motivated employees who want to play a role in helping people with serious health conditions and who see this effort as personally rewarding. In our highly entrepreneurial environment, employees are empowered and the opportunity for professional development occurs every...
The Research Associate provides daily care of research animals, including performing basic husbandry duties. Responsible for maintenance of the Animal Facility including regular facility sanitation. Performs in vivo research support duties such as sample collection, data collection, treatment dosing, and can develop new skills as required based on research needs. In addition, the Research Associate may assist with vitro assays and cell culture, schedule permitting.
The Facility Technician supports Celldex’s Fall River operations by performing maintenance on equipment within a GxP and general research facility. This facility consists of research, quality control, pre-clinical and analytical development laboratories, a GMP clinical manufacturing facility, warehouse, and office space. The technician will prioritize the workload around departmental schedules in order to complete required preventative and routine maintenance activities.
The Senior Director, Clinical Science is a strategic scientific leader responsible for shaping clinical development strategy, overseeing clinical study design, and directing the interpretation of clinical data across one or more development programs. This individual serves as a key partner to Clinical Science leadership and is accountable for advancing innovative therapies through critical development milestones, including proof-of-concept, registrational studies, regulatory submissions, and lifecycle management.
The Senior Director will provide scientific and organizational leadership across...