Job Title MW Strategy and Transformational Excellence Lead Job ID 24 02115 location Remote Duration 3 6 Months Client Strategy and Transformational Excellence lead Support Head of Global Regulatory Medical Writing Head (Client) in facilitating initiatives on building medical writing (MW) strategic presence with MW therapy area heads (TAH) and cross functional stakeholders

JOb Title Associate Scientist. Job Id 24 02124 Location East Hanover,NJ Duration 12 Months on W2 Contract Bachelor of Science Degree in relavent field. 2 years of analytical analysis experience preferred. Working as part of a project team, you support the delivery of long term research projects in line with the business and consumer needs. You plan and execute projects fr

Job Title Laboratory Assistant III Job Id 24 02126 Location East Hanover,NJ Duration 04 Months On W2 Contract A 4 year degree in a science related or similar technical field such as Food Science, Nutrition , or Science will be required. Some prior lab experience would be appreciated as well as an independent highly motivated and driven personality. Strong Computer skills

Manage and maintain Windows based servers and systems, including Active Directory and Azure environments. Design, implement, and support Active Directory infrastructure, including domain controllers, group policies, and user management. Configure and manage Azure services, including Azure AD, Azure Virtual Machines, and Azure Active Directory Connect. Implement and admini

100% Onsite position

12 Months of W2 Contract

Performs validation document generation, program management, and protocol execution activities. Interface with Engineering, and end user groups to support development of life cycle documents and system requirements. Design the validation approach with technical oversight, provide the scientific rationale and acceptance criteria, and generate validation protocols. Execute

will include, but are not limited to, the following 1. Participate in the development of the CMC regulatory strategy for post approval small molecule product submissions, including global supplements/variations and responses to health authority queries. 2. Prepare and review CMC submission documents, registration dossiers, and responses to health authorities through collab