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The role brings an exciting opportunity to work with Product management, Underwriting, Actuarial and Corporate Cat departments to define strategy and guidelines in Cat exposed regions through developing Chubb’s own view of Cat Risk. Major Duties and Responsibilities: Perform quarterly/monthly roll-up of the personal lines exposure, analyzing and monitoring catastrophe risk via third part catastrophe models, internal tools and software.
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Capital equipment sales experience along with selling consumables preferred. Qualifications: Bachelors degree preferred along with experience selling capital equipment in the Aesthetics or Dermatology space.
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Four or more years of experience in Cybersecurity, IT Audit, Internal Audit, Security & Privacy Services, Business Process Controls, IT Risk Management, SOX Advisory, or related IT or audit compliance work.
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We specialize in: Underground Utilities (Gas, Water, Sewer, Fiber Optic, Electrical), Overhead Utilities (Transmission, Distribution, and Substation), Foundations, Bridges, Highways, Airports, Drilling, Pile Driving, Sitework, Power Plants, Emergency Management, Reconstruction, 24-Hour Storm Response, Storm Hardening, Shoreline Restoration/Stabilization, Debris Removal, Solar Installation, and Construction Management.
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Johnson and Johnson Innovative Medicine is recruiting for a Director, Global Real World Evidence (RWE) in our Global Commercial Strategy Organization (GCSO). Interface outside of GCSO with the regional businesses, US RWV&E, global epidemiology, R&D, JJT, legal, HCC and others in the development of the RWE strategy and guidelines for evidence generation and usage.
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Responsible for project management of capital projects in a GMP environment. the individual will have frequent exposure to senior management as they execute projects that shape our overall strategy and transform our site into a best-in-class Biopharmaceutical facility.
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The base salary is just one component of J.Crew Group’s competitive total rewards strategy that also includes the opportunity for bonus, competitive benefits and perks. Share feedback, insights and ideas with the management team.
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Develops, implements and maintains required EHS programs, may include but not limited to lockout/tagout, confined space, respiratory protection, hazardous waste management, emergency planning and response, etc.
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Oversee the Identity and Access Management Platform – OKTA and Azure AD. Administer Illumio and Zscaler for micro-segmentation and zero trust security models to reduce attack surfaces and limit lateral movement within the network.
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Expertise with MS Office, Word, Excel and document management systems such as Veeva or Documentum is a plus. He/she/they performs life cycle management for marketed products by creating and/or evaluating change controls for global regulatory impact and planning corresponding variations/amendments/supplements.
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Establish and maintain Risk Appetite Statement, Capital Management Framework, Sensitivity Analysis, Igloo NtInsight Model Governance and other items identified as ERM Key Initiatives in collaboration with the Board of Directors and executive management.
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Oversee planning, direction, and coordination of support and maintenance for medium to large-scale integration platforms, utilizing your expertise in API Management tools, Integration platforms (e.g., MuleSoft, Boomi), and Scripting languages (e.g., Python, Bash.
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10+ years of expertise in project management, process, product, and/or analytical development activities and oncology project development. Develop (or have subordinates develop) activity plan, and budget for project in alignment with Unit strategy, plan, budget and CDP. Lead (or have subordinates lead) cross-functional product decisions including approach for tech development, manufacturing network strategy, and change control strategy/planning as chair of PAC-MT, etc.
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2+ years with a top-tier strategy consulting firm serving clients in tech and healthcare industries or in a product management role with a health tech company. The Candidate will have a proven track record of success in project and product management, with experience in developing and launching tech solutions.
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The CMC Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports. The technical writer contributes to various US, EU and rest of world (ROW) dossiers such as NDA, MAA, IND, IMPD, CTA, amendments, supplements, variations and other communications with regulatory authorities (e.g., briefing documents for meetings.
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capital management strategy jobs in Bedminster, NJ
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