- Merck & Co. (Rahway, NJ)
- …existing and pipeline products to produce safe, effective, innovative medicine.The Senior Principal Scientist/ Senior Director is responsible for protocol ... and preparation of manuscripts for publication in peer-reviewed journals. The Senior Director will also contribute to establishing Vaccine Clinical Development… more
- Genmab (NJ)
- …skills, scientific rigor, and a commitment to excellence. You thrive in a fast-paced environment , are motivated by high standards , and can lead projects with ... At Genmab, we are seeking a passionate and experienced Senior Medical Writing Manager to help us tell the...at the heart of a team that plays a critical role in bringing innovative therapies to patients-and we… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally ... other research areas centered around rare diseases and immune disorders. Summary: The Senior Director, Head of RBQM (Risk Based Quality Monitoring) sets the vision… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …you will have the opportunity to build a life-changing career in a global business environment . We encourage our employees to make the most of their talent, and we ... for Novo Nordisk Inc (NNI) in accordance with International Financial Reporting Standards (IFRS), US Generally Accepted Accounting Principles (GAAP) and Novo Nordisk… more
- Repligen (Waltham, MA)
- OverviewWe are seeking a highly skilled and motivated Senior Cell Culture Scientist to join our Advanced Bioprocess Applications R&D team. This role will focus on ... Human Embryonic Kidney 293 (HEK293) cells for viral vector production, is essential.As a Senior Cell Culture Scientist, you will play a pivotal role in advancing our… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAs a Senior Engineer in Device Design and Process Development group, you will be part of our Research & Development team that designs and develops ... manufacture of drug-device combination products.Hands on troubleshooting in a manufacturing environment with an ability to operate assembly equipment and/or assist… more
- Merck & Co. (Rahway, NJ)
- …Laboratory Quality Assurance and is accountable for the execution of critical activities in the areas of compliance, quality systems, regulatory intelligence, ... or pharmaceutical industry . - Knowledge of regulatory requirements and industry standards related to digital solutions and data in the healthcare or pharmaceutical… more
- Merck & Co. (Upper Gwynedd, PA)
- …new data becomes available.Monitor and evaluate model performance in a production environment , while ensuring compliance with industry standards and best ... to manage multiple tasks and meet deadlines in a fast-paced environment .Effective verbal and written communication skills for conveying complex information to… more
- Merck & Co. (North Wales, PA)
- …and report programming development and validation utilizing global and TA standards and following departmental SOPs and good programming practices Maintain and ... field plus 5-9 years SAS programming experience in a clinical trial environment MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally ... execution of key safety initiatives aimed at preventing, mitigating, and addressing critical safety issues including but not limited to protocol amendments, Dear HCP… more
- Merck & Co. (Rahway, NJ)
- …our Device Development & Technology (DD&T) organization to serve as a senior technical subject matter-expert and advisor for our Autoinjector platform. This role's ... the entire lifecycle from early development through lifecycle management, providing critical technical strategic oversight and guidance across all teams involved in… more
- Merck & Co. (Rahway, NJ)
- …oversight of all high priority programs - and studies. Adhere to our company's standards and R&D/ GCD and GCTO goals, initiatives and - expectations. Participate and ... support the goals and objectives of the GCTO Senior Leadership - Team (SLT) or extended Leadership Team...achieve GCTO, GCD, and R&D objectives. Set clear performance standards and holds self and - organization accountable for… more
- Merck & Co. (Rahway, NJ)
- …recruitment.Creates an empowering, compliant, collaborative, and innovation-focused work environment .Builds a culture of quality and compliance through training, ... GCD / GCTO goals, initiatives and expectations.Development and delivery of company standards in given geography.Activities of all cluster/country level GCTO team &… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally ... Buy and Bill distribution models. Expertise in these are critical and align with the strategic vision of evolving...to deliver the materials.Will be required to partner with Senior Training Leadership in the identification and selection of… more
- Merck & Co. (Rahway, NJ)
- …state-of-the-art technology and applying rigorous scientific and ethical standards .-The Distinguished Scientist (Executive Director) and Product Development Team ... to oncology compounds.-The Executive Director/PDT lead may:-Manage Directors and/or Senior Directors responsible for Oncology Global Clinical Development projects.-Supervise… more
- Merck & Co. (Durham, NC)
- …products is manufactured, tested, packaged, stored, and distributed according to high standards of quality and in compliance with all regulatory requirements. -The ... Senior Specialist, Quality Assurance will support ongoing efforts to...year of experience in aseptic manufacturing or another cleanroom environment .Strong contemporary knowledge of relevant current Good Manufacturing Practices… more
- Merck & Co. (North Wales, PA)
- …for the benefit of patients and global human health.Responsibilities: The Senior Statistical Programmer, Submission Data Standards Quality Management (SDS ... vaccine clinical development projects. Accountability predominantly includes submission data standards planning activities, coaching and consulting with project teams,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJob Description The Senior Scientist, Device Design Control Lead, is a crucial member of our team, responsible for spearheading design control efforts ... through launch and post-market surveillance. Key Responsibilities and Activities: The Senior Scientist, Device System - Device Design Control will be responsible… more
- Merck & Co. (Rahway, NJ)
- …analysis and reporting deliverables under the guidance of a senior -level programmer supporting early-phase oncology clinical trials. Collaborate with other ... Contribute to the development and validation of datasets following CDISC standards . Generate tables, listings, and graphics required for clinical trial… more
- Merck & Co. (Rahway, NJ)
- …listings, figures and submission deliverables under the guidance of a senior level programmer.Perform validation tasks according to departmental SOPs and collaborate ... plus at least 2 years SAS programming experience in a clinical trial environment . Required experience and skills Must possess SAS programming skills including data… more
