Director, Regulatory Labeling
$176.66k - $229.43kCelldex Therapeutics, Inc.
About Celldex 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 day. Overview Celldex Therapeutics is seeking an experienced Regulatory Affairs professional with demonstrated expertise in product labeling and promotional regulatory review to support development and commercialization activities across its portfolio. This individual will serve as the regulatory labeling lead, providing strategic and operational oversight for US prescribing information, core labeling documents, and promotional materials to ensure compliance with FDA regulations and company policies.The successful candidate will be part of the regulatory team and partner closely with Clinical Development, Medical Affairs, Commercial, Legal, Pharmacovigilance, and Quality teams to develop, maintain, and implement labeling strategies throughout the product lifecycle. Responsibilities Regulatory Labeling StrategyLead development and maintenance of US Prescribing Information (USPI), Patient Package Inserts (PPI), Medication Guides, Instructions for Use (IFU), Carton and container labeling, Company Core Data Sheets (CCDS)Define labeling strategies for INDs, BLAs, sBLAs, and post-approval changesEvaluate clinical, nonclinical, and safety data for labeling impactEnsure consistency across global labeling documentsDigital and social media contentCongress materialsDisease awareness campaignsCross-Functional LeadershipPartner across Clinical, PV, Medical, Commercial, Legal, and Quality teamsProvide regulatory guidance throughout development and commercializationLead cross-functional labeling initiativesCompliance & Process ImprovementMonitor evolving FDA requirementsMaintain SOPs for labeling and promotional reviewSupport inspections and auditsDrive continuous improvement within Regulatory Affairs Qualifications Bachelor’s degree in Life Sciences, Pharmacy, Regulatory Affairs, or related field required; advanced degree (MS, PharmD, PhD, JD) preferred 10+ years of Regulatory Affairs experience, including 5+ years leading labeling strategy for development and/or commercial products Proven experience developing and maintaining labeling documents (USPI, CCDS, Medication Guides, and packaging components) Experience supporting INDs, BLAs, and post-approval submissions, including participation in MLR/PRC review processes Strong knowledge of FDA labeling regulations, OPDP requirements, and promotional review guidance Experience with commercial-stage products; immunology or biologics background preferred Demonstrated success leading FDA labeling negotiations and driving strategic regulatory initiatives Strong scientific/clinical interpretation, communication, and cross-functional influence skills Excellent project management and organizational abilities, with capacity to thrive in a fast-paced biotech environmentCompensationThe expected base salary range for this position is $176,659 to $229,427We 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 outreachJob Summary
$225k - $275k
...we evolve to win in self-care.Description OverviewAs Senior Director of Regulatory Affairs - Cluster (North America), you are accountable for... ...regulatory governance is applied to submissions, claims, and labelling decisions Regional VigilanceAccountable for regulatory...SuggestedWork at officeLocal areaRemote work2 days per week- ...LinkedIn, Facebook, Instagram, X and YouTube. Job Description The Director Regulatory Affairs Global Regulatory Lead (GRL II), Global Regulatory... ...and content of global regulatory dossiers. May lead the Labeling Regulatory Strategy Team (LRST). Serves as the primary regulatory...SuggestedWork at officeWorldwide
- ...monitoring of PLAIR activities, prior to new product launch Manage regulatory correspondence mainly to CDER, FDA, User fee staff, drug... ...process, derived from regulatory correspondences. Support TA Labeling team, when required. Participate in decision making process with...SuggestedLocal area
$233.63k - $373.2k
...Affairs Leadership Team, the Executive Director, Medical Affairs will serve as a subject... ...medical safety) to inform study designs, labels, and postmarketing commitments.Medical communications... ...to translate complex data for clinical, regulatory, commercial, and access stakeholders....Suggested$108.5k - $201.5k
...commercial content, working closely with Brand, Medical, Legal, Regulatory, and agency partners to enable confident decisions, reduce risk... ...timely asset removal aligned to expiration, withdrawal, or label changes.Contribute to MAP forecasting and capacity planning to...SuggestedFull timeRemote workRelocation- Responsibilities Define and lead the regional regulatory execution priorities Translate Category regulatory strategies into actionable market execution plans Lead engagement with FDA and Health Canada Own cluster regulatory delivery performance and set submission priorities...
- ...This individual will be responsible for providing strategic regulatory advice and oversight for all of Altimmune's US regulatory applications... ...relevant clinical, nonclinical, advertising, promotional, and labeling aspects of relevant US regulatory submissions, responses, and...Local areaRemote work
- ...and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description• Assist and support regulatory CMC managers in the following activities:• Defining global CMC regulatory strategy and decisions for development projects or marketed...Immediate start
- ...Participate in a multidisciplinary technical team to develop regulatory strategies and solutions for a wide range of Crop Protection &... ...with the creation of NVA numbers for new and revised technical labels, and locating most current versions available of these, as needed...Local area
$153.62k - $245.39k
...operates with independence, accountability, and execution focus in a fast-paced, performance-driven biotech environment.The Associate Director is expected to deliver complex, data-driven scientific discussions, synthesize meaningful insights from the field, and navigate...Work from homeHome office$225k - $275k
...Perrigo journey as we evolve to win in self-care. As Senior Director of Regulatory Affairs - Cluster (North America), you are accountable for... ...governance is applied to submissions, claims, and labelling decisions Regional Vigilance Accountable for regulatory...Work at officeLocal areaRemote work2 days per week$141k
...collective strength of a unified team. Join the team in making better possible for patients everywhere. Summary The Associate Director, Regulatory Operations is responsible for driving the execution of global regulatory strategy, ensuring alignment with health authority...For contractorsWork at officeLocal areaFlexible hours$90k - $200k
...management and enhancement of client relationships. Plan and manage a broad range of complex investigations, forensic accounting, regulatory compliance, including business intelligence, internal (client) investigations, insider risk compliance assessments, consulting...Temporary workFlexible hours- ...Head of Regulatory Affairs About the Company Respected provider of top-quality services Industry Consumer Services Type... ...of expertise in FDA regulations, particularly in the areas of labeling, claims, and formulation, and requires a strong background in...
$108.5k - $201.5k
...and financial processes evolve, and bring clarity to complex regulatory and audit landscapes. This role offers the opportunity to grow... ...collaboratively across functions and levels, including Associate Director and Director stakeholdersProven capability to manage multiple...Full time$70k - $150k
...member of the Financial Investigations team Take an active role on a broad range of complex investigations, forensic accounting, regulatory compliance, internal (client) investigations, insider risk compliance assessments, consulting projects and forensic matters, with...Temporary workInterim roleFlexible hours- ...people. Every essence of you enriches our world. We are Givaudan. Human by nature.Join us as our next Head of Systems Strategy - Regulatory, reporting to our Global Head of Regulatory Compliance & Digital Strategy. We are looking for an experienced Solution Lead with a...
- Responsibilities Responsible for all aspects of the organization’s corporate compliance program and associated fraud, waste, and abuse prevention initiatives. Manage the day-to-day activities of the Compliance Division. Develop and update written internal standards of ...
- ...provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job DescriptionResponsible for implementing regulatory strategy and managing operational activities for assigned regions.Provides input into global regulatory strategy, including...Work at officeImmediate startWorldwide
$103k - $129k
...drivers to leadership. This position will report to the Associate Director, Government Pricing & Compliance.How You’ll Spend Your... ...attributes across internal and external platforms to support regulatory review and reporting for both new product launches and existing...Contract workTemporary workLocal areaWorldwideFlexible hours$116.16k - $150.85k
...and submission of the Biologics License Application (BLA), and subsequent commercial activities.The ideal candidate brings strong regulatory judgment, hands‑on QA expertise, and a proactive leadership mindset focused on inspection readiness, compliance excellence, and...Contract work$225k - $275k
...Perrigo is seeking a Sr Director of Regulatory Affairs for North America, based in Morristown, NJ. This pivotal role focuses on regulatory activation and engagement with health authorities to drive business growth. The ideal candidate will have extensive regulatory experience...Work at officeRemote work$100k - $150k
...and 1 day remote where it makes sense to do so. The Company is an equal employment opportunity employer. Responsibilities As our Regulatory Compliance Manager , you’ll report to the operating unit General Counsel and is responsible for designing, executing and overseeing...Full timeWork at officeRemote work$185.5k - $344.5k
...Job Description SummaryThe Director, Portfolio and Pipeline Strategy, will support the TA Head, GM and the ED, Portfolio & Pipeline Strategy... ...(LCM) planning for new indications, formulations and labels for in-line products as well as Integrated Evidence Plans and LCM...Full time- Withum is a place where talent thrives - where who you are matters. It’s a place of endless opportunities for growth. A place where entrepreneurial energy plus inclusive teamwork equals exponential results.Explore different industries. Learn new skills. Connect with our...Full timeContract workWork at officeLocal area
$100k - $150.86k
OverviewColliers Engineering & Design is looking for a Project Manager to join our Planning Discipline within the Buildings Engineering Services Division in New Jersey! This individual will manage, direct, and supervise the work efforts of assigned staff and coordinate ...Temporary workWork at officeNight shift- Director of Compliance Responsible for all aspects of the organization’s corporate compliance program and associated fraud, waste, and... ...areas (whether such risks are predefined by regulation or regulatory guidance, or identified through organizational experience) for...
- Director of Compliance Responsible for all aspects of the organization's corporate compliance program and associated fraud, waste, and... ...areas (whether such risks are predefined by regulation or regulatory guidance, or identified through organizational experience) for...For contractorsFor subcontractor
- A leading construction brand is seeking a Director, Legal to serve as the sole legal advisor. This role requires over 10 years of corporate... ...governance, manage litigation and contracts, and ensure regulatory compliance. The position involves global travel and requires a...
- ...of the Südzucker Group. Your Responsibilities Drive Food Regulatory Affairs activities, submissions, and processes for the US & Canada... ...independently assess regulatory requirements related to food labelling, claims, ingredient status, and customer inquiries relevant to...Full time
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