- ThermoFisher Scientific (New Brunswick, NJ)
- …Research Group can advance your career, apply now! The main focus of the Validation Analyst (also referred to as a Scientific Software Compliance Specialist) ... will be to provide validation support for local and global regulated ...lab environment with a clear understanding of GMP laboratory operations and testing _In some cases an equivalency,… more
- J&J Family of Companies (Raritan, NJ)
- Analyst 1 Quality Control Stability Laboratory ...& Johnson's Family of Companies, is recruiting for an ** Analyst I, Quality Control - Stability Lab ** ... in our pharmaceutical products? Apply today for this exciting opportunity! The Analyst I is responsible for conducting stability testing in accordance with… more
- AbbVie (Branchburg, NJ)
- …fixation and stain techniques. Operate, maintain, and assist in qualification/ validation activities of standard laboratory /histology equipment (microtome, ... Instagram, YouTube and LinkedIn. Job Description The Histology Associate Analyst is responsible for proficiently performing and documenting histological testing… more
- Kedrion Biopharma, Inc. (Melville, NY)
- …process samples, raw materials, finished products, stability, and process validation samples; completes pertinent documentation associated with activities; and ... expected to support other described functions as necessary. + Support laboratory management by contributing with: 1. Conduct housekeeping (eg, QC Fridges/Incubator,… more
- US Bank (New York, NY)
- …liquidity, market, operational, reputational, strategic, and other risks as appropriate. Validation Analysts within MRM provide independent validation of models ... relies on for making financial decisions. A robust and comprehensive model validation includes steps that independently challenge a model's conceptual framework and… more
- Pfizer (Pearl River, NY)
- …with assay validation and regulatory compliance + Experience in laboratory management including inventory and sample tracking, analyst scheduling, oversight ... create high-throughput, validated, diagnostic assays in a regulated environment. The lab follows Standard Operating Procedures and cGLP (current Good Laboratory… more
- Actalent (Newark, NJ)
- …and assists with the development of protocols, informed consent forms, monitoring and validation plans. + Oversees submission of IND Application to FDA as needed. + ... Designs case report forms and liaises with data analyst for database development. + Coordinates study manuals of procedures for site coordinators, pharmacists, and … more