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Provide engineering and testing support for mobile infrastructure solutions, develop mobility strategic vision, work with IT teams, wireless carriers, and vendors, assist in developing new mobility services offerings, represent Mobility Infrastructure Services on projects, improve customer support, and provide training.
Develop technical solutions for capital projects in HVAC and Mechanical Utility system design. Collaborate with project teams and external partners to meet business objectives. Provide technical guidance, author engineering design standards, support start-up planning, and troubleshoot HVAC issues. Mentor junior engineers and stay updated with industry trends. Operate within project constraints.
The Associate Director - HVAC Engineer will lead or support project HVAC design efforts, provide technical guidance to project teams, ensure deliverables meet standards, collaborate with external partners, troubleshoot HVAC issues, mentor junior engineers, and stay updated on industry technology trends.
Provide technical manufacturing assistance in engineering, maintenance, and utilities. Support vaccine manufacturing processes, equipment maintenance, and troubleshoot issues to ensure reliable operations. Ensure compliance with GMP quality, safety, and environmental standards.
Primary site contact and site manager for clinical research studies in the Northeast region, responsible for site relationships, monitoring activities, and regulatory compliance. Requires 2 years of clinical research experience and a degree in science/biology.
The Associate Clinical Research Associate in the Northeast Region (Remote) will act as the primary site contact and site manager for clinical research studies, ensuring compliance with protocols and regulations. Responsibilities include site management, monitoring activities, maintaining documentation, and coordinating with various stakeholders.
Act as primary site contact and site manager for clinical research studies, ensuring compliance with protocols and regulations. Coordinate tasks, conduct site visits, collect regulatory documentation, and communicate with investigators and site staff. Manage information systems and support audit activities as needed.
Primary site contact and site manager for clinical research studies, ensuring compliance with regulations and protocols. Conducts site monitoring activities, manages regulatory documentation, communicates with site staff, and resolves site performance issues. Requires travel domestically and internationally. Qualifications include fluency in languages, clinical research knowledge, and IT skills.
Primary site contact and site manager for clinical research studies, conducting site management activities, ensuring protocol compliance, and communicating with site staff and investigators. Responsible for site selection, validation, and oversight activities. Requires travel.
The Quality Assurance Associate Director will provide critical support in overseeing Incoming Material Release and Sterility Assurance teams, ensuring compliance with regulations, cGMP, and Quality Management System. Responsibilities include managing teams, maintaining facility and personnel control, providing QA support, and leading cross-functional teams. Required experience includes a Bachelor's degree in related fields with 7 years of experience or a Master's degree with 5 years of experience, along with strong decision-making and problem-solving skills.
The Director of US Lifecycle and Loss of Exclusivity (LOE) Management will define and implement the lifecycle management and LOE strategy for the Oncology portfolio, collaborating closely with cross-functional teams to ensure successful implementation. Responsibilities include developing scenarios, collaborating with the OCAR team, and monitoring key changes. The role requires 10+ years of pharmaceutical commercial experience and the ability to influence and collaborate effectively.
Seeking an Associate Director, TT Systems Group Leader with 7 years of experience in project and team management. Responsibilities include leading a team in technical transfer systems for large molecules, ensuring systems are maintained and improved, managing project schedules, and fostering effective communication with stakeholders. This role also involves coaching and developing employees, ensuring compliance with regulatory requirements, and driving process improvements.
Seeking a highly motivated Associate Director, Technology Transfer Systems Group Leader with expertise in managing TT systems, project management, and leadership. Responsible for end-to-end technical transfer systems for large molecules. Must demonstrate deep expertise in people management, TT standards, and best practices. Will collaborate with various departments and contribute to business process improvements and ongoing TT activities.
The Specialist, Operations supports manufacturing operations in the Vaccines HPV Bulk IPT organization, ensuring compliance with regulations and implementing lean manufacturing initiatives. This role involves problem-solving, project management, and resource management to achieve business results.
The Associate Director of Forecasting will be responsible for developing strategic forecasts for products and indications, interpreting implications, and communicating insights to drive marketing strategy. They will collaborate with various functions to build a strong market perspective and deliver forecasting insights.
The Associate Director of Forecasting will be responsible for developing strategic forecasts for products and indications, interpreting implications, and communicating insights to the business. They will collaborate with various functions to build market perspective and deliver forecasting insights. The ideal candidate will have expertise in forecasting methodologies, strong business acumen, and the ability to work across functions. Strong communication, management, and continuous learning skills are essential for this role.
Primary site contact and site manager throughout all phases of a clinical research study, ensuring site relationships, monitoring activities, site visits, regulatory documentation, and communication with site staff. Ability to travel 65%-75% of working time domestically and internationally. Requires a B.A./B.S. with 2 years of clinical research experience.
Act as primary site contact and site manager throughout all phases of a clinical research study. Develop relationships with sites, perform site management activities in compliance with regulations, coordinate tasks with sponsors, conduct monitoring activities, ensure data accuracy & subject safety, manage regulatory documentation, communicate with investigators, resolve site problems, collaborate with various teams, and maintain documentation in systems.
Primary site contact and site manager for clinical research study, ensuring compliance with regulations and protocols. Develops site relationships, conducts monitoring activities, and manages documentation. Travels domestically and internationally. Requires fluency in local languages and English, communication skills, and knowledge of clinical research practices.
Primary site contact and site manager for clinical research study, ensuring site relationships, coordinating tasks, conducting site visits, and managing regulatory documentation.
