- Merck & Co. (Rahway, NJ)
- Job Description Associate Director of Product Management, Patient Insights Engine- We are seeking an Associate Director of Product Management in the Commercial ... leader put together business cases to secure buy-in and alignment with our senior leaders to secure the necessary funding to manage the product throughout its… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director, Global Cardiometabolic Communications will be part of the Global Pharma communications team and will collaborate closely with ... in support of the US- and global cardiometabolic business.The Associate Director will report to the Director, Global Cardiometabolic...and pop culture around the world to engage in new approaches to reach consumers on important disease awareness… more
- Novo Nordisk Inc. (Durham, NC)
- …maintains a curious and pioneering spirit, harmonious with our growing pipeline of new products and emerging technologies. What we offer you: Leading pay and annual ... Shift. Responsible for the production activities & validation. Ensuring relevant compliance issues are addressed & handled in close collaboration with production.… more
- Merck & Co. (Millsboro, DE)
- Job DescriptionOur company seeks to add an Associate Director. Veterinarian Services at our Millsboro, Delaware location. This position will have overall ... at our company's Millsboro Animal Health facilities. This role is highly compliance -driven in accordance with State and Federal regulations as applicable to the… more
- Merck & Co. (Rahway, NJ)
- …backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.Our ability to excel depends on the integrity, ... selected candidate will play a pivotal role in supporting both current and new business transformation projects within the CSS organization. You will bring the… more
- Merck & Co. (Rahway, NJ)
- …to join the Global Safety Center of Excellence (CoE) team as an Associate Director, Safety Programs CoE.- This individual will be responsible for the management ... and manage company's safety standards and technical guidelines to ensure compliance and reduction in workplace safety risks.Lead global continuous improvement… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. In addition to a strong portfolio of medicines for ... areas centered around rare diseases and immune disorders. JOB SUMMARYThe Associate Director, GMP QA Process Excellence is accountable to collect information,… more
- Merck & Co. (Lower Gwynedd, PA)
- …while developing and expanding your career.We are seeking a highly motivated Senior Scientist to join the Department of Pharmacokinetics, Dynamics, Metabolism, and ... art technologies and is expected to champion applied evaluation of new technologies and lead implementation to expand vaccine response knowledge, increase… more
- Merck & Co. (Rahway, NJ)
- …as a subject matter expert in a particular area of expertise Mentors new team members and supports staff development, as needed Demonstrates high capability to ... communicate with stakeholders at various levels, including cross-functional teams, senior management, external vendors, and clinical sites. Strong negotiation,… more
- Merck & Co. (Rahway, NJ)
- …valued colleagues across our Company enterprise.- - - Position Description - The Associate Director is responsible for identifying and driving improv ements to the ... site utility infrastructure and work processes at the Rahway, New Jersey Site .- This role will support facility...both office personnel and research operations . - The Associate Director will serve as a key liaison between… more
- Merck & Co. (Rahway, NJ)
- Job Description Position Description: Associate Director, Financial Evaluation & Analysis (FE&A) Primarily responsible for all aspects of financial evaluation and ... to communicate results to financial and non-financial management.Investigate potential new financial analysis techniques to determine whether currently used… more
- Aequor (Thousand Oaks, CA)
- 100 % onsite Thousand Oaks The ideal candidate for the MCS Senior Material Coordinator role would be one with prior experience in pharmaceuticals, medical devices, ... other GMP-regulated industry, with a solid understanding of GMP compliance and SOP adherence. They would need to have...amount of SOP reading, warehouse familiarization and training. A new hire is typically trained to full competency in… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. In addition to a strong portfolio of medicines for ... regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines. The Senior Clinical Study Manager will have routine interaction with key… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …quality, resources, and stability, uniting the best of both worlds to develop new medicines for patients. We recognize that improving human health starts here and ... 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)
- …areas and routes of administration, including inhalation, implantation, and injection.The Associate Principal Scientist will lead the definition and execution of ... and successfully execute against design verification strategies.Stay current with new device technologies, relevant worldwide regulations, standards, and effectively… more
- Merck & Co. (Rahway, NJ)
- …by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.Global Real Estate Strategy is a strategic corporate ... and innovative real estate and workplace solutions aligned with corporate strategy.The Associate Director of Real Estate Strategic Planning will play a crucial… more
- Aequor (Thousand Oaks, CA)
- …Day Responsibilities: Ensure all work is completed with minimal disruption and in compliance with all cGMP guidelines and procedures. Apply standard Supply Chain and ... quantities etc.) Review and rationalize Bill of Material (BOM) requirements for new and existing products. Responsible for the coordination of logistics activities,… more
- Merck & Co. (Rahway, NJ)
- …and create presentations for visible projects for a broad range audience ( senior leadership - local teams) Liaise and build relationships with local/regional site ... plans, and pilots specific to a region to support new ways of working. Keep current with emerging trends...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …the FDA to providing medical education and collecting data to support efficacy and new product development, CMR is involved. The one thing that keeps us all marching ... a living. Are you ready to make a difference? The Position The Associate Director, Regulatory Affairs - Advertising & Promotion will provide strategic regulatory… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. In addition to a strong portfolio of medicines for ... listings, SAP, Data Mgmt plan; Reviews patient population and protocol compliance for consistency with study strategy; Develops biomarker strategy in collaboration… more
