- Merck & Co. (Durham, NC)
- Job DescriptionThe Senior Project Manager is responsible for providing project management support for our Company manufacturing sites in Durham, North ... Carolina. This position will be part of the new Site Project Management Office team.Primary responsibilities include, but are not limited to, the following:Manage… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …As a result, this role will need to partner closely with teams and senior leaders from across Regulatory Affairs, as well as cross-functional stakeholders (eg, ... business requirements for reporting and analyticsEngage with key stakeholders, including Regulatory Affairs teams and cross-functional project team members, to… more
- Merck & Co. (North Wales, PA)
- …is responsible for developing medical writing deliverables that support the clinical regulatory writing portfolio. With minimal oversight, the Senior Medical ... investigator's brochures, clinical sections of submissions) per company and regulatory requirements.Applies an in-depth knowledge of medical writing responsibilities,… more
- Merck & Co. (North Wales, PA)
- …of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.- Specifically, the Senior Director ... talented and dedicated colleagues while developing and expanding your career.The Senior Clinical Director (Sr. Principal Scientist) has primary responsibility for… more
- Merck & Co. (Durham, NC)
- Job DescriptionJob DescriptionThis role is within a capital project start-up in Durham, North Carolina. The new facility will include end-to-end processing of drug ... and warehouse.-As the team finishes design and construction of the facility, the Senior Technician will play a critical role in supporting the Global Engineering… more
- Merck & Co. (Rahway, NJ)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... and coordinating statistical activities supporting drug/vaccine projects.Interacts with Clinical, Regulatory , Statistical Programming, Data Management, and our Company's Research… more
- Merck & Co. (Rahway, NJ)
- …of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, The Senior Director May ... talented and dedicated colleagues while developing and expanding your career.The Senior Director (Sr. Principal Scientist) has primary responsibility for the… more
- Merck & Co. (North Wales, PA)
- …and simulation stakeholders spanning all of our company's therapeutic areas. The senior programmer will gather and interpret user requirements, retrieve the required ... be a key collaborator with modelers, statisticians and other project stakeholders.Primary Activities:Programmatically synthesize preclinical / clinical data into… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionWe are seeking applications for a Senior Scientist position available at the Rahway, NJ research facility. Join Small Molecule Analytical Research and ... and dedicated colleagues while developing and expanding your career.In your role as Senior Scientist, you will be part of a team developing innovative analytical… more
- Merck & Co. (North Wales, PA)
- …information that they need.Providing mentoring, coaching, and oversight to Specialist and Senior Specialist project managers working on common projects. Sharing ... Job DescriptionThe drug development Project Manager is part of Global Project...strategic and tactical input from diverse disciplines (eg, clinical, regulatory , market access, manufacturing, CMC, commercial, and other areas)… more
- Merck & Co. (Rahway, NJ)
- …and developments align with business requirements, industry standards, and regulatory compliance.Define and enforce change control processes and methodologies to ... needs and align SAP solutions accordingly.Act as a trusted advisor to senior management, providing insights and recommendations on leveraging SAP capabilities to… 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
- Novo Nordisk Inc. (Boulder, CO)
- …analytical and process development, the CMC team works alongside Quality, Regulatory , Technical Operations and RNAi Early Development professionals at our Boulder, ... are driving change. Are you ready to make a difference? The Position The Senior Manager of Specialty Raw Materials Manufacturing is responsible for ensuring a steady… more
- Eisai, Inc (NJ)
- …If this is your profile, we want to hear from you. Job Summary The Senior Manager, Medical Writing will be the designated Lead Medical Writer for approximately 3-4 ... protocols, and protocol amendments often acting as the compound leadLead project management for medical writing deliverable by defining milestones, managing budget,… more
- Merck & Co. (Durham, NC)
- …life-saving medicines and vaccines, including our HPV vaccines. - The Senior Engineering Specialist will troubleshoot and maintain process and process support ... review/approval, and review of contracts. Interact with vendors and support project coordination activities like FAT, SAT, Design Reviews, and Engineering… more
- Merck & Co. (Durham, NC)
- Job DescriptionWe are seeking a Growth and Improvement minded- Senior Maintenance Technician - HVAC & Refrigeration that can help drive our Strategic Operating ... - They are a Competitive Advantage for UsSummary, Focus and Purpose The Senior Maintenance Technician - HVAC & Refrigeration is accountable for providing maintenance… more
- Merck & Co. (Rahway, NJ)
- …department of our Research & Development Division is seeking applicants for a Senior Scientist position available at our research facility. The Senior Scientist ... program deadlines.Authoring and reviewing internal technical reports, sections of regulatory filings (eg, IND, BLA) and external scientific publications.Strong… more
- Merck & Co. (Durham, NC)
- Job DescriptionThe Senior Maintenance Technician is responsible for providing equipment troubleshooting and maintenance support for a new product feasibility ... project /manufacturing support. Support updates to standard operating procedures (SOP's)...multi-stage refrigeration systems) Required Experience and f amiliarity of regulatory requirements in accordance with GMP manufacturing operations Preferred… more
- Eisai, Inc (Nutley, NJ)
- …make a difference. If this is your profile, we want to hear from you. Senior Manager, US Alzheimer's Strategy and Lifecycle Planning Marketing will assist with the ... business partners and external agenciesPotentially Lead or Co-lead cross-functional project teams involving Marketing, Sales, Managed Markets/Market Access, Legal, … more
- Merck & Co. (South San Francisco, CA)
- …reports. Interact with colleagues from multiple areas, including discovery, regulatory affairs, project teams, and development functions.Partner with ... DescriptionJob Responsibilities:Primary responsibility is writing and preparing nonclinical pharmacology regulatory document submission sections and study reports to support… more
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