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The 2nd Shift Core Site Services Engineering Specialist is responsible for providing technical manufacturing assistance in the field of engineering, maintenance, and utilities. They will support day-to-day engineering operations, troubleshoot process equipment, and ensure compliance with quality, safety, and environmental standards. This role also involves leading maintenance programs, root cause analysis, reliability improvement, and project management for small projects within the manufacturing facility.

Provide engineering and testing support for mobile infrastructure solutions, develop mobility strategic vision, work with IT teams and vendors, assist in developing new mobility services, represent services on projects, and improve customer support.

Primary site contact and site manager for clinical research study, ensuring protocol adherence, site relationships, data accuracy, and regulatory compliance. Supports audit/inspection activities and collaborates with various stakeholders for study success.

The Associate Clinical Research Associate in the Northeast Region (Remote) acts as the primary site contact and manager throughout all phases of a clinical research study, ensuring site relationships, compliance, and data quality. They coordinate tasks, conduct monitoring activities, and support site performance in collaboration with various stakeholders.

Primary site contact and site manager throughout all phases of a clinical research study, responsible for developing site relationships, conducting monitoring activities, and ensuring protocol compliance. Requires travel domestically and internationally approximately 65%-75% of working time.

Primary site contact and site manager throughout all phases of a clinical research study. Conducts site management activities in compliance with regulations and protocols. Performs remote and on-site monitoring to ensure data accuracy and subject safety. Manages regulatory documentation, communicates with site staff, and resolves site performance issues. Works collaboratively with various departments and external parties to support assigned sites. Requires ability to travel domestically and internationally. Fluent in Local Languages and English. Good understanding of clinical research, GCP, and clinical trial guidelines.

Lead the lifecycle management and loss of exclusivity (LOE) strategy for the Oncology portfolio, collaborating with cross-functional teams to ensure successful implementation. Develop scenarios and strategies based on key variables and events. Maintain insights on customers, competitors, and the market environment to inform strategic initiatives.

Seeking a highly motivated Associate Director for Technology Transfer Systems Group Leader role in Large Molecule Technology Transfer. Responsible for leading a team in end-to-end technical transfer systems for technology transfers of large molecules. Key responsibilities include managing TT systems activities, maintaining project schedules, ensuring clear communication with stakeholders, developing training programs, and complying with global and regulatory requirements.

The Quality Assurance Associate Director at Teknika oversees the Incoming Material Release and Sterility Assurance teams to ensure compliance with cGMP, regulations, and quality standards. Responsibilities include managing teams, ensuring facility and personnel compliance, providing QA support, and leading cross-functional teams.

The Specialist, Operations role supports manufacturing operations in ensuring compliance with regulations, continuous improvement, and lean manufacturing initiatives. Responsibilities include business expertise, problem solving, decision making, project management, and resource management.

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 work closely with various functions and stakeholders to build a strong market perspective and deliver forecasting insights.

The Associate Director of Forecasting will develop strategic forecasts for products and indications, interpret implications, and communicate insights to support marketing strategy. They will work closely with various functions and stakeholders to deliver forecasting insights and drive business decisions.

Primary site contact and manager for clinical research studies, responsible for site relationships, site management, monitoring activities, and ensuring protocol compliance. Participates in site selection, validation, and oversight activities, as well as regulatory documentation. Communicates with Investigators and site staff, resolves site performance issues, and collaborates with various internal and external stakeholders.

Primary site contact and site manager for clinical research studies, ensuring compliance with protocols and regulations. Conducts site visits, manages tasks with sponsor roles, and communicates with Investigators on protocol conduct and performance. Manages documentation and information in various systems. Ability to travel domestically and internationally.

Primary site contact and site manager for clinical research study, ensuring compliance with protocols and regulations. Conducts site visits, monitors data quality, and communicates with site staff and Investigators. Manages regulatory documentation and collaborates with internal and external stakeholders.

As an Associate Clinical Research Associate, you will act as the primary site contact and manager throughout all phases of a clinical research study. Responsibilities include site management, monitoring activities, ensuring compliance with regulations, and maintaining documentation.

The Associate Director, OCAR Planning and Operations in the US Oncology field focuses on planning, execution, and business improvement within the OCAR organization. Responsibilities include collaborating across teams, driving business efforts, monitoring KPIs, leading change management, and managing a ~$30MM budget for promotional initiatives. This role requires 5 years of experience in Business Operations, Pharmaceutical Marketing, Finance, Customer Management, or Policy within the pharmaceutical or life sciences industry.

Associate Director, Customer Engagement & Multi-Channel Marketing responsible for leading communications plans, directing creative development process, and driving marketing strategies for Companion Animal global launches. Key responsibilities include developing customer journeys, market mapping, defining customer personas, and ensuring consistency in marketing planning and execution processes.

The Animal Care Technician Level 2 works under the guidance of a Vivarium manager to support translational models impacting drug safety assessment and human health. Responsibilities include animal care, maintenance, handling, and documentation in compliance with regulations and procedures.

The Director, DSCS Digital Program Manager will advance the purpose and aspiration of our Company's DSCS Digital Strategy to enable a seamless data infrastructure that drives increased speed, capacity, and robustness across organizational deliverables. Responsibilities include defining scope, building plans, tracking progress, partnering with IT, facilitating meetings, and monitoring projects in adjacent digital landscapes.