- Merck & Co. (Rahway, NJ)
- …to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on ... reliable, and compliant medical products, practices and solutions to the world.-The Associate Principal Scientist Regulatory Affairs supports products in the… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and initiatives to develop solutions to promotional issues, while ensuring regulatory compliance and effectively managing business risks Creatively advise ... you ready to make a difference? The Position The Associate Director, Regulatory Affairs - Advertising &...mitigation strategies to meet overall business need, while maintaining compliance with US regulatory requirements and company… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …to make a difference? The Position We are seeking a dynamic and experienced Regulatory Affairs Labeling Associate Manager to oversee and lead critical tasks ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...regulatory guidance on commercial labeling materials to ensure compliance with CFR and FDA labeling requirements Identify labeling… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product ... labeling in collaboration with Global Regulatory Leads (GRLs). This position may serve as an...development or approval for either the US or EU.Ensure Compliance with Core Data Sheets/Label Changes: Manages updates to… more
- Merck & Co. (Rahway, NJ)
- …development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions. The Pharmacometrics group within QP2 brings an experienced ... of decision-making at our company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas.This Associate … more
- Merck & Co. (Rahway, NJ)
- …clear communication, protocol transfer, quality agreements, secure data transfer, and regulatory compliance .Proficiency in handling primary cells derived from ... within TMB is seeking a highly motivated and skilled individual for the Associate Principal Scientist position. This role is vital for the development, validation,… more
- Merck & Co. (Rahway, NJ)
- …Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical Development ... clinical pharmacology and pharmacometrics of oncology drugs from post-PCC to registration. Associate Directors are emerging leaders in the field of quantitative drug… more
- Merck & Co. (Rahway, NJ)
- …sites, manufacturing investigations, process validation, and authoring of regulatory submissions. -Under the general scientific and administrative direction ... next generation process development and characterization, process validation, and regulatory submission authoringIn this role, the successful candidate will be… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …include brand marketing, market access, Enterprise Insights, sales, medical/CMR, legal, compliance , and regulatory . Other internal relationships include Public ... contractual arrangements, SOPs, KPIs, and budget. Ensure adherence to all compliance and regulatory requirements Fiscal management: Demonstrate fiscal discipline… more
- Merck & Co. (Millsboro, DE)
- …and unregulated species including chickens, turkeys, dogs, cats, rabbits, and rodents.Assure compliance with all federal and state regulatory requirements for ... Job DescriptionOur company seeks to add an Associate Director. Veterinarian Services at our Millsboro, Delaware location. This position will have overall… more
- Merck & Co. (South San Francisco, CA)
- …company's Research Laboratories in South San Francisco is seeking an Associate Principal Scientist with strong expertise in translational cell models, mechanistic ... analysis, and reporting to project teams, governance bodies, and regulatory agencies.Drive scientific innovation and champion new enabling technologies and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …to ensuring the highest standards of scientific integrity, patient safety, regulatory compliance , and collaboration across therapeutic areas. Ultimately, this ... lives for a living. Are you ready to make a difference? The Position The Associate Global Medical Director will serve as a pivotal leader in advancing the mission of… more
- Merck & Co. (Rahway, NJ)
- …products. Our team is looking for a candidate for the position of Associate Principal Scientist (R4) focused on developing parenteral drug products across a range ... packaging, compatibility characterization for processing and administration, and supporting regulatory filings. Build deep fundamental knowledge around the drug… more
- Merck & Co. (North Wales, PA)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The incumbent is responsible for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …cross-functional teams in the analysis and redesign of business processes. Ensure compliance with regulatory standards (eg, ICH, FDA, or other industry-specific ... areas centered around rare diseases and immune disorders. JOB SUMMARYThe Associate Director, GMP QA Process Excellence is accountable to collect information,… more
- Merck & Co. (Rahway, NJ)
- …Analytical Research and Development (SMAR&D) group has an exciting opportunity for an Associate Principal Scientist based in Rahway, NJ. Join us and experience our ... talented and dedicated colleagues while developing and expanding your career.-- As an Associate Principal Scientist, you will be part of a team develop ing… more
- Merck & Co. (Lower Gwynedd, PA)
- …as well as selecting and designing applicable assays capable to meet regulatory expectations for vaccine or biologics development. The candidate should be current ... concepts and interest in associated hands-on laboratory experimentation. Follow compliance requirements including GxP regulations. Contribute to assay protocol and… more
- Merck & Co. (Rahway, NJ)
- …areas and routes of administration, including inhalation, implantation, and injection.The Associate Principal Scientist will lead the definition and execution of ... Company and with external partners.Author and review relevant portions of the regulatory submissions (INDs, IMPDs, NDAs, BLAs, etc.) for combination product programs… more
- Merck & Co. (Rahway, NJ)
- …as a lead GCS Planning program representative ) such as clinical development, regulatory , quality and other supply chain areas to negotiate timelines ,- strategies ... consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents… more
- Merck & Co. (Durham, NC)
- …over the last several years; currently Durham employs 1,000+ people.Durham's Associate Technician, Operations will be responsible for supporting the manufacturing ... or related fieldExperience with on-the-floor cGMP manufacturing and familiarity with regulatory requirementsDemonstrated ability to work both independently and as a… more
