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Design, development of bioanalytical assays and subsequent sample analysis of study samples for discovery biologics portfolio. Execute bioanalytical assays using platforms such as Gyrolab, MSD, ...
Associate Scientist will be responsible for supporting analytical activities within Biologics Process Development (PD). The role will involve supporting in-process analytical testing, delivering ...
Scientist position in LC-MSResponsibilities:Position is full-time, Monday-Friday, 8 a.m.-5 p.m., with overtime as needed. Candidates currently living in MA are encouraged to apply. Responsible for ...
This role is responsible for collecting, preparing, delivering and managing Module 1 documents in support of international market registrations through lifecycle to ensure accurate, consistent, and ...
Description: Research Associate - CLMD PREREQUISITES: Bachelor’s degree with 0-4 years of experience working in a laboratory setting is preferred. Responsibilities include, but are not ...
Performs administrative and/or physical tasks involved in the shipping, receiving, storing, and distributing of products/inventory Tracks all movement and handling of products in a computerized ...
Support Medical Safety Assessment Physicians (MSAP) in leading Safety Data Review (SDR) Teams. Appropriately perform core signal detection activities, elevate program or portfolio issues impacting ...
Second Shift (3:30 pm to 11:30), require overtimeDescription: Job Title: Laboratory Technician IIDepartment: QualityReports to: QA LaboratoryJob Responsibilities:1. To complete laboratory analytical ...
WW Scientific Content & US Market Capabilities Contractor, Cardiovascular Description: The primary responsibility for the WW Scientific Content & US Market Capabilities Manager is the ...
Functional Area Description: Responsible for all regulatory activities related to assigned products in the role as Regulatory Manager. Support IC Regulatory Strategic operations Head. Position ...
The RIM Specialist will be a subject matter expert in the Regulatory Information Management (RIM) system with focus on actlivties like Planning, tracking and monitoring activities related to ...
This position provides biomarker bioanalytical support for ligand binding assay methods. This scientist provides laboratory support for assay and method development, assay validation and study ...
Location will be between the Morris Plains and East Hanover sites during the week. This position is required to be onsite 100% Foster & support a team culture that is engaged and ...
Perform Quality Control testing for in-process, release, stability, water, and raw material in a cGMP environment. It is preferred that the candidate have analytical experience including but ...
Participate as part of a cross functional global project to qualify QC instruments and associated software. Support the implementations of a new standardized global qualification for QC ...
Must Have: Experience in cross functional project management (preferably CMC) Familiarity with end to end CMC drug development with an understanding of critical milestones and typical ...
The centralized TMF organization is responsible for the completeness and accuracy of the Trial Master File for all company-sponsored studies. The group will deliver technical expertise in the ...
The Manager,Clinical Data Management is a leadership role considered essential to the sustainability and success of the company's R&D pipeline This role reports into Associate Director, ...
Qualifications: • Bachelor’s Degree in Microbiology or Biology. • Minimum of 1 - 2 years of experience in biopharmaceutical industry, preferably working in a quality control ...
The Manufacturing Support Assistant Process Engineer will support Manufacturing Operations (Upstream/ Downstream processing, cryogenics facility, facilities, and materials management) on a daily ...
