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

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

Job Title Maintenance Contract Team Lead I Job Id 24 02282 Location East Hanover,NJ Duration 06 Months On W2 Contract Lab Management and Maintanence Tech Degree or BS (no specific area) Responsible for ensuring Equipment Calibration & Maintenance (scheduling, keeping records) Ingredient Management/Lab Space Management /Lab GMP Common raw materials restock Lab materials re

Hybrid Role

Job Title Rheumatology Review Group Eligibility Liaison Job ID 24 02297 Location Madison, NJ, 07940 Duration 12 Months contract on W2 Job Description Job Title Rheumatology Review Group (RRG) Eligibility Liaison Division R&D / Global Drug Development Functional Area Description The RRG Eligibility Liaison (REL) employs scientific and technical expertise to track, coordina

Job Title Facility, Utility, and Equipment Reliability Specialist Job ID 24 02189 Location Warren, NJ Duration 12 Months contract on W2 Onsite Role Work Schedule Mon Fri, Business Hours Flexibility is required though as needs of the business warrant Position Overview The main purpose of the Facility, Utility, and Equipment Reliability Specialist is to evaluate facility an

12 Months of W2 Contract

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