Associate Manager, Regulatory & Scientific Affairs International Flavors & Fragrances IncAssociate Manager, Regulatory & Scientific AffairsWilmington, DEli>Prepare, review, and submit regulatory dossiers and filings, including Generally Recognized as Safe (GRAS) notices, New Dietary Ingredient Notifications (NDINs), Product License Applications (PLAs), Master Files, and Chemistry, Manufacturing, and Controls (CMC) documentation. This role is part of global regulatory focus teams and partners closely with R&D, Quality, Commercial, Marketing, and Legal stakeholders to ensure regulatory compliance while enabling product development, manufacturing, and commercialization.
NewNorth American Regulatory Affairs Specialist International Flavors & Fragrances IncNorth American Regulatory Affairs SpecialistWilmington, DEp>Health & Biosciences: Channeling our passion for nature and bioscience into sustainable, life-enhancing technologies that power innovative solutions across healthcare, food, consumer and industrial markets. Prepare and contribute to regulatory submissions, including Generally Recognized as Safe (GRAS), Association of American Feed Control Officials (AAFCO), and Canadian feed (CFIA) approvals.
Regulatory Affairs Specialist Dentsply Sirona IncRegulatory Affairs SpecialistDEDentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands. Key Responsibilities: Prepares and submits international regulatory submissions to obtain and maintain regulatory approvals for medical devices, including 510(k) submissions and technical files for CE Marking.
Director Promotional Regulatory Affairs AstraZeneca PlcDirector Promotional Regulatory AffairsWilmington, DEDesirable Skills/Experience: • Advanced degree in life sciences, pharmacy, law, or a related discipline • 10 or more years of experience in US promotional regulatory affairs within biopharma, including direct OPDP/APLB interactions and resolution of advisory or enforcement matters • Experience leading or co-chairing MLR processes and operating within digital review systems such as AZAP or comparable platforms • Launch-to-lifecycle leadership across HCP and consumer promotions, managed markets materials, and omnichannel/digital campaigns • Proven ability to design and deliver effective regulatory training for commercial and medical stakeholders • Demonstrated influence at senior levels to shape departmental practices and operational plans • People leadership experience with a track record of coaching and building high-performing teams. Essential Skills/Experience: • Bachelor's degree in science • 3+ years' experience in promotional regulatory affairs, FDA (OPDP/APLB), or other equivalent experience in advertising and promotion review • 5+ years total experience in pharmaceutical/biotech industry, FDA, or equivalent experience • Strong knowledge of FDA promotional regulations and ability to apply such knowledge in review of diverse promotional materials and audiences • Knowledge of the drug development and labeling processes.
Senior Regulatory Affairs Specialist Dentsply Sirona IncSenior Regulatory Affairs SpecialistDEFor California Residents: We may collect the following categories of personal information in connection with the submission of your resume or application materials to us for employment, and if hired, your employment with us: identifiers (e.g., name, address, email address, birthdate); personal records (e.g., telephone number, signature, education information, criminal background information, passport number and visa information); consumer characteristics (e.g., sex, marital status, veteran status, race, disability, sexual orientation); professional or employment information (e.g., resume, cover letter, employment history, background check forms, references, certifications, transcripts and languages spoken); and inferences from personal information collected (e.g., a profile reflecting abilities and aptitudes). The above categories of personal information are collected for the following business purposes: performing recruitment and hiring services; processing interactions and transactions (e.g., to comply with federal and state laws requiring us to maintain certain records, managing the workforce); and security (e.g., detecting security incidents, protecting against fraudulent or illegal activity).
Associate Director, International Regulatory Affairs Incyte CorpAssociate Director, International Regulatory AffairsWilmington, DEJob Summary Primary function The Associate Director International Regulatory Affairs works in collaboration with International Regulatory Affairs Lead to develop regulatory strategies with multi-functional teams and partners and ensures that International Regulatory Requirements for assigned products are complete. Provide appropriate regulatory strategies to support submission of marketing and life-cycle applications may also include support of clinical trial applicationsexpanded access programs in International Markets Provides regulatory support to inter-departmental project teams.
Senior Manager, Government & Industry Affairs Operations VGW Holdings LtdSenior Manager, Government & Industry Affairs OperationsDelaware, DERemote$200,000–$230,000 / yearYou will be responsible for bringing structure, discipline, and clear operating rhythm to a complex, multi state lobbying network, ensuring our external partners are well coordinated, accountable, and aligned to business priorities. We have an exciting opportunity to join our Government & Industry Affairs team in the United States and are currently looking for a Senior Manager, Government & Industry Affairs Operations to join the team.
Manager, Facilities Blood Bank of DelmarvaManager, FacilitiesNewark, DelawareConnect with us on Facebook, X, Instagram, and LinkedIn. .
NewProject Manager - Healthmark QMS, Defined Term (Remote in EST) Getinge ABProject Manager - Healthmark QMS, Defined Term (Remote in EST)Dover, DERemote$120,160–$150,000 / yearp>Required Knowledge, Skills and Abilities: Expert-level working knowledge of FDA 21 CFR Part 820 / Quality Management System Regulation (QMSR), including its incorporation of ISO 13485:2016 effective February 2026. The project manager will serve as the primary driver of project(s) execution across a group of QMS workstreams, coordinating cross-functional teams and ensuring delivery against defined milestones.
Environmental Health and Safety Manager DuPont de Nemours IncEnvironmental Health and Safety ManagerNewark, DEWhat We're Looking For Required Qualifications Bachelor's degree in Environmental, Health & Safety, Occupational Safety & Health, Environmental Science, Industrial Engineering, or related discipline Certified Safety Professional (CSP) 5-10 years of EHS experience in manufacturing or industrial environments Strong working knowledge of OSHA, EPA, state safety and environmental regulations, workers' compensation, and injury reporting Demonstrated experience in: Hazard identification and risk assessments Incident investigation and root cause analysis Regulatory compliance and environmental permitting/reporting Contractor safety management Preferred Qualifications OSHA certifications ISO 14001, ISO 45001, and/or Certified Industrial Hygienist (CIH) Experience supporting high‑hazard processes * Proven leadership, collaboration, and communication skills Join our Talent Community to stay connected with us! Why Join Us | DuPont Careers Environmental, Health & Safety (EHS) Manager Make an Impact Where Safety, People, and Operations Come Together We are seeking an experienced Environmental, Health & Safety (EHS) Manager to lead the development, implementation, and continuous improvement of site‑wide EHS and Industrial Hygiene (IHS) programs.
Designer Chesapeake Utilities CorpDesignerDover, DEul>Assist the Engineering Manager - Planning & Design on various design projects, prioritize project schedules and staff assignments. Facilitates project development in conjunction with District Operations and Sales & Marketing, including managing and prioritizing project design schedules.
SUPERVISOR III QMS TE Connectivity plcSUPERVISOR III QMSMiddletown, DEThis role leads Quality Systems activities including document control, training compliance, CAPA coordination, internal and external audits, management review processes, and continuous improvement initiatives. The Quality Systems Supervisor is responsible for overseeing and maintaining the site Quality Management System (QMS) to ensure compliance with applicable regulatory requirements, customer expectations, and internal procedures.
NewSenior Specialist - Technology and Cybersecurity Risk - Enterprise Data M&T Bank CorpSenior Specialist - Technology and Cybersecurity Risk - Enterprise DataWilmington, DE$136,000–$226,600 / yearp>Scope of Responsibilities: This role primarily interacts with senior people leaders within the Technology and Cybersecurity teams, senior people leaders of Technology and Cybersecurity Risk, and internal partners such as the Risk Division, Internal Audit, and Regulatory Affairs. Develop and execute sophisticated risk management frameworks and programs that align Enterprise Data practices with business objectives and regulatory requirements, including leading risk and control self‑assessments and summarizing complex findings for leadership.
Research Program Director of Environmental Health and Safety NemoursResearch Program Director of Environmental Health and SafetyWilmington, DEFull timeWe deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships. The position provides support and guidance in the development and implementation of institutional and laboratory/protocol-specific procedures and protocols, as well as conducting hazard assessments and responding to emergencies involving hazardous materials.
Executive Medical Director, Global Risk Management & Safety Surveillance Incyte CorpExecutive Medical Director, Global Risk Management & Safety SurveillanceWilmington, DEThe position will require strong oversight for patient safety issues that arise at both the individual and aggregate levels within the company and in collaboration with co-development and business partners strong decision-making skills on all issues involving safety assessment and surveillance responsibility for compliant timely and complete regulatory authority engagement with particular emphasis on benefit-risk assessments and risk identificationcharacterization and mitigationmanagement and effective communication of safety information to internal and external stakeholders. Through the discovery development and commercialization of proprietary therapeutics Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology Oncology and Inflammation and Autoimmunity Headquartered in Wilmington Delaware Incyte has operations in North America Europe and Asia.
ISWM First Line Risk Issue Management and Remediation Coordinator Wilmington TrustISWM First Line Risk Issue Management and Remediation CoordinatorWilmington, Delawarep>Bachelor’s degree and a minimum of 3 years' relevant work experience, or in lieu of a degree, a combined minimum of 7 years' higher education and/or work experience, including a minimum of 3 years' relevant work experience. M&T Bank is committed to fair, competitive, and market-informed pay for our employees.
ISWM First Line Risk Issue Management and Remediation Coordinator M&T Bank CorpISWM First Line Risk Issue Management and Remediation CoordinatorWilmington, DE$82,100–$136,900 / yearp>Education and Experience Required: Bachelor's degree and a minimum of 3 years' relevant work experience, or in lieu of a degree, a combined minimum of 7 years' higher education and/or work experience, including a minimum of 3 years' relevant work experience. Overview: This role provides support to a range of activities within the First Line Risk Management function, with focus on the Institutional Services & Wealth Management business line.
Medical Writer II/ Sr Medical Writer Syneos HealthMedical Writer II/ Sr Medical WriterDelawarep style="text-align:inherit"/>Salary Range: $70,100.00 - $145,000.00The base salary range represents the anticipated low and high of the Syneos Health range for this position. Interacts and builds good working relations with clients, department head, and peers in data management, biostatistics, regulatory affairs, and medical affairs, as necessary, to produce writing deliverables.
Contracting Specialist, Research Office University of DelawareContracting Specialist, Research OfficeNewark, DEThe Contracting Specialist addresses a wide spectrum of research-related issues associated with the University's research enterprise by working on a multitude of agreements, evaluating intellectual property issues, staying current on research-related regulations, ensuring compliance with federal regulations and University policies, and interacting with research faculty, research administrators for Research & Regulatory Affairs and other members of the Research Office staff. The Contracting Specialist addresses a wide spectrum of research-related issues associated with the University's research enterprise by reviewing a multitude of agreements, evaluating intellectual property issues, staying current on research-related regulations, ensuring compliance with federal regulations and University policies, and interacting with research faculty and University of Delaware units.
Methods Specialist Merck & Co IncMethods SpecialistMillsboro, DE$79,200–$124,700 / yearParticipate in or lead cross-functional teams for site-to-site analytical method transfers: establish transfer plans, assess site readiness, and manage timelines, risks and deliverables with support from senior team members. Perform bench-level remediation across multiple test platforms, including live bacterial and virus titration/identification and ELISA for complex multivalent vaccines and in-process materials, working under guidance from senior team members.