41 personal risk jobs found

Biogen About This Role As a Sr. Engineer III in Manufacturing Sciences, you will be an integral member of the global Manufacturing Sciences team. Your primary focus will be on leading, facilitating, and coordinating biologic molecule technology (tech) transfer activities at our Bio Site in RTP. You will create, drive, and communicate technology transfer deliverables while managing the overall tech transfer schedule and metrics. By utilizing technical rigor, analyzing complex issues and identifying business process optimization opportunities, you will provide technical leadership, strategic insights and direction. Your role also involves communicating transfer plans and risk mitigations to senior leadership, ensuring alignment with departmental priorities. This position is pivotal for driving successful tech transfers, supporting both internal programs and those of our strategic partners, and enhancing the value to our business What You'll Do: Coordinate and lead tech...

Merck Job Description Role Summary The Director, Cyber AI Engineering is a senior technical leader responsible for architecting and delivering production-grade AI systems that power autonomous cyber defense and enterprise security automation. Reporting to the Director of Cyber AI & Automation, this role leads the design and implementation of scalable AI decision engines, behavioral analytics systems, and agent-based automation integrated directly into enterprise security platforms. This is a hands-on technical leadership role. The Director will design systems, guide engineering execution, and ensure AI capabilities are production-ready, governed, and safely integrated into enforcement workflows. Core Responsibilities AI Systems Architecture Design scalable AI architectures capable of ingesting and reasoning over high-volume enterprise telemetry. Lead engineering of behavioral analytics, anomaly detection, and risk scoring models. Define...

Merck Job Description Role Summary The Director, Cyber AI Engineering is a senior technical leader responsible for architecting and delivering production-grade AI systems that power autonomous cyber defense and enterprise security automation. Reporting to the Director of Cyber AI & Automation, this role leads the design and implementation of scalable AI decision engines, behavioral analytics systems, and agent-based automation integrated directly into enterprise security platforms. This is a hands-on technical leadership role. The Director will design systems, guide engineering execution, and ensure AI capabilities are production-ready, governed, and safely integrated into enforcement workflows. Core Responsibilities AI Systems Architecture Design scalable AI architectures capable of ingesting and reasoning over high-volume enterprise telemetry. Lead engineering of behavioral analytics, anomaly detection, and risk scoring models. Define...

Merck Job Description The Facilities Management team delivers services that enrich our workplace and strengthen our organizational culture, while supporting the evolving needs of our business and stakeholders. We are committed to creating great workplace experience and maintaining reliable, safe, and compliant operations. Through the solutions and services we provide, we enable employees to innovate, collaborate, explore new ideas, anddeliver impactful results. Responsible for leading, directing, and coordinating all facilities and site support operations across Corporate Headquarters and Technical R&D sites. Scope includes accountable oversight of all site operations and amenities, including master planning, soft services, security operations, utility generation and distribution and related infrastructure, warehouse operations, wastewater and potable water systems, maintenance and repair, laboratory support services, and management of the Integrated Facilities...

Merck Job Description We aim to create workplace experiences that enable our people to be inspired to invent. Inside our organization, we provide workplace solutions that enable our people to do their very best work in safety. Outside our organization we ensure we protect the people around us, communities and the environment. Position Summary The Associate Director, Emergency Management, is responsible for providing strategic leadership, oversight, and management of the Security Command Center, Emergency Response Operations, and the General Emergency Management System (GEMS) Plan for the Elkton, VA facility. This role ensures the site's readiness to prevent, prepare for, respond to, and recover from emergencies while maintaining compliance with all applicable security, fire and life safety, and emergency preparedness regulations and standards. The position works closely with Plant Protection cross-functional teams to effectively and safely operate and maintain the...

Merck Job Description As a Device and Clinical Package Design Engineer, you will be part of our R&D team that develops drug delivery systems and designs secondary packaging for combination products in clinical space. Key Responsibilities: Demonstrates working knowledge of combination product devices. Experienced in the design, development, and performance testing of secondary packaging for combination products with demonstrated experience operating packaging CAD programs (Solidworks and Artios) to design machinable, sustainable packaging solutions with deliverable solutions which perform in distribution testing. Designs, prototypes, conducts testing and analyzes data to inform design development activities. Has experience in design verification specifically focused on package distribution testing for combination products Can specify standards for packaging materials not limited to paperboard and corrugate as well as packaging equipment for label...

Merck Job Description We aim to create workplace experiences that enable our people to be inspired to invent. Inside our organization, we provide workplace solutions that enable our people to do their very best work in safety. Outside our organization we ensure we protect the people around us, communities and the environment. Position Summary The Associate Director, Emergency Management, is responsible for providing strategic leadership, oversight, and management of the Security Command Center, Emergency Response Operations, and the General Emergency Management System (GEMS) Plan for the Elkton, VA facility. This role ensures the site's readiness to prevent, prepare for, respond to, and recover from emergencies while maintaining compliance with all applicable security, fire and life safety, and emergency preparedness regulations and standards. The position works closely with Plant Protection cross-functional teams to effectively and safely operate and maintain the...

Merck Job Description Our ability to excel relies on the innovation, integrity, expertise and teamwork of our scientists. We value rigorous scientific exploration, cross-functional collaboration, creative-thinking and dedication to building strong and operationally excellent teams. As part of our industry-leading drug development programs, you will have the opportunity to collaborate with highly talented and dedicated colleagues, working urgently to develop lifesaving medicines and vaccines and deliver the next medical breakthroughs. The Analytical Research & Development department of our Company Research Laboratories Division is seeking an experienced and highly-motivated Principal Scientist with extensive cell-based characterization assay development expertise. The successful candidate will have experience with the design, execution and optimization of a broad range of characterization assays and be responsible for development of analytical control strategies for...

Merck Job Description The Facilities Management team delivers services that enrich our workplace and strengthen our organizational culture, while supporting the evolving needs of our business and stakeholders. We are committed to creating great workplace experience and maintaining reliable, safe, and compliant operations. Through the solutions and services we provide, we enable employees to innovate, collaborate, explore new ideas, anddeliver impactful results. Responsible for leading, directing, and coordinating all facilities and site support operations across Corporate Headquarters and Technical R&D sites. Scope includes accountable oversight of all site operations and amenities, including master planning, soft services, security operations, utility generation and distribution and related infrastructure, warehouse operations, wastewater and potable water systems, maintenance and repair, laboratory support services, and management of the Integrated Facilities...

Biogen About This Role: As the Associate Director, Field Clinical Engineering, you will play a pivotal role in the Implantable Device Unit, supporting the Head of Device Clinical. This position is integral to the development and daily management of field clinical activities, leading the Field Clinical Engineering (FCE) team. You will be at the forefront, interacting with neurologists, surgeons, and other stakeholders, fostering robust relationships with investigators and key opinion leaders. Your leadership will be crucial in hiring, developing, and motivating the FCE team, ensuring a culture of accountability and professional excellence. By coordinating field operations and serving as a key contact for clinical issues, you will act as a bridge between clinical research, commercial sites, and internal stakeholders. Your collaboration with Device Development, Clinical, Regulatory, and other teams will ensure the successful execution of clinical trials, contributing...

Biogen The Director, Clinical Operations Program Leadership (COPL) is responsible for leading the strategy, planning and implementation of clinical development program operations in the Clinical Trial Delivery Unit of the Quantitative Science Development Operations organization (QSDO). The COPL is a key contributor as the lead program level QSDO representative to the Development Asset Team (DAT) and as called upon to the Product Development and Commercialization team (PDC). This individual is responsible for providing advanced functional and technical expertise and insights from both a strategic (decision points, risk) and operational (timeline scenarios, feasibility & financials) perspective to meaningfully contribute and make recommendations to Integrated Asset Plans (IAP), clinical development plans, and other key plans and initiatives necessary to advance Biogen clinical programs. The COPL is accountable for the strategy, planning, oversight and delivery of program level...

Biogen The Director, Clinical Operations Program Leadership (COPL) is responsible for leading the strategy, planning and implementation of clinical development program operations in the Clinical Trial Delivery Unit of the Quantitative Science Development Operations organization (QSDO). The COPL is a key contributor as the lead program level QSDO representative to the Development Asset Team (DAT) and as called upon to the Product Development and Commercialization team (PDC). This individual is responsible for providing advanced functional and technical expertise and insights from both a strategic (decision points, risk) and operational (timeline scenarios, feasibility & financials) perspective to meaningfully contribute and make recommendations to Integrated Asset Plans (IAP), clinical development plans, and other key plans and initiatives necessary to advance Biogen clinical programs. The COPL is accountable for the strategy, planning, oversight and delivery of program level...

Biogen This position is on site at our Research Triangle Park, NC facility, and would include 20-30% travel, domestic and internationally About This Role The Senior Manager reports to the Global VTR Leader and is responsible for leading the VTR Biochemistry team at our biologics site, focusing on strategy, operations, and cross-functional alignment, overseeing analytical method development, optimization, validation, transfer, registration, investigation, and lifecycle management for late stage clinical and commercial products at internal/external sites and contract labs. The Senior Manager will prepare and review regulatory filings and respond to health agency requests (RtQs) using a risk-based approach. The senior manager also manages project prioritization, timelines, resources, and budgets and ensures compliance with global analytical strategies, CAPA, change control, deviations, and quality standards (GMP). The senior manager approves reports, analyzes data, and...

Biogen About This Role: As Biogen's Access Management Service Delivery Manager (SDM) you are the Access Management subject matter expert and services leader for all Access Management activities at Biogen. This role is accountable for delivering value to global stakeholders - which includes access services to every application in Biogen. A peer to this role is the Service Delivery Manager of Identity. This role is a direct report of the Global Leader of Identity and Access Management and is a member of the extended leadership team within the Cybersecurity organization. As Access Management SDM, you are responsible for establishing access management policies and standards and keeping them current. You are responsible for the planning and execution of initiatives that improve access management capabilities - both central platforms or efforts supporting independent stakeholder applications. This role is responsible for the entire service delivery process, from planning and...

Biogen This position is hybrid to our Cambridge MA location and requires frequent on-site presence About This Role: As the Associate Director, US Forecasting, you will be a vital member of the Decision Sciences - Forecasting Center of Excellence team, tasked with developing and maintaining precise forecast models for Biogen North America's franchises. Your expertise will drive accurate predictions using both primary and secondary data assets, offering valuable insights for strategic planning and resource allocation across multiple indications. This role involves cross-functional collaboration to gather inputs, socialize outputs, and execute sensitivity and ad hoc analyses. You will empower the business to build objective forecasts and scenarios that enable data-driven decisions, maximizing shareholder value. Reporting to the Senior Director, Forecasting COE, this position offers a blend of analytical, strategic, and operational work, allowing you to engage with stakeholders...

Biogen About This Role The Senior Director, Development Asset Lead (DAL) is responsible for leading one or more preclinical or clinical-stage assets within Biogen's development portfolio. This role provides strategic, cross-functional leadership to maximize asset value and ensure effective execution of the integrated asset plan (IAP). The DAL partners across research, development, and commercial functions to align scientific strategy, operational execution, and business considerations such as time, risk, and value. As leader of the asset team, the DAL drives development strategy, oversees progress toward key milestones, and represents the program within governance forums. This role reports to the Head of Development Asset Leadership and is responsible for guiding the most complex or late-stage assets, including programs approaching regulatory filing or major stage-gate decisions. What You'll Do Lead development and continuous refinement of the integrated asset plan to...

Nuvalent, Inc. The Company: With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building. The Role: Reporting to the Associate Director, Clinical Operations, the Manager, Clinical Operations will ensure excellence in clinical trial planning, execution, and data collection, in accordance with regulatory guidelines. They will be responsible for aspects of clinical study conduct, including site selection, study start-up, conduct and close-out. Providing appropriate escalation of trial specific issues to deliver high quality clinical trial results. Able to adapt to changes in the work environment and manage competing demands. Responsibilities: Manage multiple aspects of clinical...

Nuvalent, Inc. The Company: With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building. The Role: Reporting to the Associate Director, Clinical Operations, the Manager, Clinical Operations will ensure excellence in clinical trial planning, execution, and data collection, in accordance with regulatory guidelines. They will be responsible for aspects of clinical study conduct, including site selection, study start-up, conduct and close-out. Providing appropriate escalation of trial specific issues to deliver high quality clinical trial results. Able to adapt to changes in the work environment and manage competing demands. Responsibilities: Manage multiple aspects of clinical...

Biogen About This Role: As a Senior Pharmacovigilance (PV) Lead, you will provide strategic and operational PV/safety support for Biogen's West Coast Hub development programs, working closely with cross-functional colleagues. This Director level position is pivotal in overseeing global safety operations, ensuring high-quality pharmacovigilance deliverables, and offering expert guidance across the organization. You will manage internal and external PV resources, lead cross-functional safety governance, and serve as a subject matter expert for safety strategy across clinical development, regulatory filings, and post-marketing activities. This role is integral to the business structure, fostering collaboration and advancing the strategic safety objectives of the organization. What You'll Do: Manage internal PV personnel and external resources, including full oversight of all PV vendor activities to ensure operational excellence and compliance. Build (where applicable) and...

Nuvalent, Inc. The Company: With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building. The Role: Reporting to the Chief Legal Officer, the VP, Compliance, will serve as the company's senior compliance leader, responsible for designing, implementing, and overseeing a comprehensive and effective global healthcare compliance program aligned with applicable laws, regulations, and industry standards. The role is both strategic and hands-on: ideal for a leader who can set vision while rolling up their sleeves to build processes from the ground up. The VP, Compliance will be a trusted advisor to Nuvalent leadership and a partner across business units. Responsibilities: Partner...