Paralegal managing trademark portfolio for General Counsel's office at Merck. Preparing and filing trademark applications, supporting prosecution, and coordinating with foreign counsel.

At MSD, known as Merck & Co., Inc., Rahway, NJ, USA in the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world.
For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines.
We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals.
We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities.
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Paralegal managing trademark portfolio for General Counsel's office at Merck. Preparing and filing trademark applications, supporting prosecution, and coordinating with foreign counsel.
Technology Support Technician providing high - quality technical support to customers using our products. Working mostly from the office but with on - site visits when needed for complex issues.
Associate Director leading compensation operations and strategy development at Merck's global HR. Managing compensation processes, reporting, and stakeholder training within a cross - functional team.
Associate Principal Scientist supporting in vitro pharmacology for early drug discovery in various locations across the U.S. Collaborating with CROs and overseeing scientific workflows in a hybrid work model.
Senior Specialist in Compliance risk monitoring for pharmaceutical company. Involves data analysis and collaboration across global teams for risk management.
Associate Director leading Global Regulatory Affairs and Clinical Safety for pharmaceutical partnerships. Coordinating cross - functional activities to maintain regulatory obligations and compliance.
Associate Director leading packaging development for small molecule products, collaborating across CMC areas and ensuring compliance with regulatory standards. Responsible for defining and executing overall packaging strategies.
Managing operations of assigned application portfolios in the IT Technology Center. Ensuring operational excellence and adherence to industry standards in healthcare technology.
Associate Principal Scientist supporting outcomes research in Hematology to enable patient access to innovations. Collaborating with cross - functional teams to generate real - world evidence and improve patient health.
Product Analyst supporting Patient Safety and Quality & Compliance at global healthcare leader. Collaborating with international teams to deliver high quality IT solutions and drive innovation.
Clinical Systems Quality Manager overseeing quality activities in GxP automated systems compliance. Collaborating with IT and business stakeholders to maintain high standards and effective processes.
Associate Principal Scientist supporting statistical programming activities for drug/vaccine clinical development projects. Ensure timely and high - quality deliverables while collaborating with global teams.