Celldex
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Associate Director, Regulatory CMC
role at
Celldex . We are seeking an experienced and strategic
Associate Director of Regulatory CMC
to lead regulatory Chemistry, Manufacturing, and Controls (CMC) activities for
combination products
(drug-device). The ideal candidate will bring deep expertise in
BLA submissions ,
Module 3 authoring and review , and the regulatory landscape for combination product development and manufacturing. This role reports to the Head of Regulatory CMC and will play a key part in shaping regulatory strategies, preparing high-quality submissions, and supporting product approvals across a diverse combination product portfolio. Responsibilities Develop and execute global Regulatory CMC strategies for drug-device combination products throughout development and commercialization. Author, review, and finalize Module 3 (Quality) sections for regulatory submissions including INDs, BLAs, and global dossiers. Serve as Regulatory CMC lead on cross-functional teams to ensure alignment across all CMC aspects. Drive preparation for and participation in regulatory agency meetings, addressing CMC-related queries and managing agency interactions effectively. Qualifications Minimum 8+ years of Regulatory CMC experience, with direct experience authoring and reviewing Module 3 content for INDs/BLAs. 3+ years of experience with combination products (drug-device) and deep understanding of applicable regulatory guidance. Strong track record in leading successful BLA submissions. Exceptional writing, analytical, and project management skills. Preferred Qualifications Familiarity with drug delivery devices (e.g., prefilled syringes, autoinjectors). Experience with eCTD publishing platforms and document management systems. Global regulatory experience, especially EMA, Health Canada, PMDA, or other major markets. Compensation The expected base salary range for this position is $181,043 to $190,827. We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market. Compensation for this role includes base salary, annual discretionary bonus, long term incentive, 401(K) plan with employer contribution, health care and other insurance benefits (for employee and family), paid holidays, vacation, and sick days. A summary of our benefits can be found on our careers page. Celldex is proud to be an equal opportunity employer that strives to foster a culture of diversity, equity, and inclusion. We are committed to promoting a diverse environment through development, recruiting and community outreach. We are committed to maintaining a respectful and inclusive workplace and to equal opportunity in all aspects of employment.
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Associate Director, Regulatory CMC
role at
Celldex . We are seeking an experienced and strategic
Associate Director of Regulatory CMC
to lead regulatory Chemistry, Manufacturing, and Controls (CMC) activities for
combination products
(drug-device). The ideal candidate will bring deep expertise in
BLA submissions ,
Module 3 authoring and review , and the regulatory landscape for combination product development and manufacturing. This role reports to the Head of Regulatory CMC and will play a key part in shaping regulatory strategies, preparing high-quality submissions, and supporting product approvals across a diverse combination product portfolio. Responsibilities Develop and execute global Regulatory CMC strategies for drug-device combination products throughout development and commercialization. Author, review, and finalize Module 3 (Quality) sections for regulatory submissions including INDs, BLAs, and global dossiers. Serve as Regulatory CMC lead on cross-functional teams to ensure alignment across all CMC aspects. Drive preparation for and participation in regulatory agency meetings, addressing CMC-related queries and managing agency interactions effectively. Qualifications Minimum 8+ years of Regulatory CMC experience, with direct experience authoring and reviewing Module 3 content for INDs/BLAs. 3+ years of experience with combination products (drug-device) and deep understanding of applicable regulatory guidance. Strong track record in leading successful BLA submissions. Exceptional writing, analytical, and project management skills. Preferred Qualifications Familiarity with drug delivery devices (e.g., prefilled syringes, autoinjectors). Experience with eCTD publishing platforms and document management systems. Global regulatory experience, especially EMA, Health Canada, PMDA, or other major markets. Compensation The expected base salary range for this position is $181,043 to $190,827. We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market. Compensation for this role includes base salary, annual discretionary bonus, long term incentive, 401(K) plan with employer contribution, health care and other insurance benefits (for employee and family), paid holidays, vacation, and sick days. A summary of our benefits can be found on our careers page. Celldex is proud to be an equal opportunity employer that strives to foster a culture of diversity, equity, and inclusion. We are committed to promoting a diverse environment through development, recruiting and community outreach. We are committed to maintaining a respectful and inclusive workplace and to equal opportunity in all aspects of employment.
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