THE LARGEST COLLECTION OF PHARMACEUTICAL JOBS ON EARTH
Supports PDF, DOC, DOCX, TXT, XLS, WPD, HTM, HTML files up to 5 MB
Requisition ID: ENG004251Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, ..
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and ..
Project Manager Regulatory Affairs
At Abbott, we're committed to helping people live their best possible life through the power of health. For more than ..
... innovative and robust team of manufacturing, Research and Development and commercial ... to one of twelve commercial manufacturing sites globally and the only ... globally and the only commercial..
Project Management Methodology
927 million. That’s how many lives our products touched in 2017. And while we’re proud of that, in this world of ..
Pharmaceutical Development Technician
Bristol Myers Squibb
The goal of the pharmaceutical development within Research & Development is to develop new drug candidates and the ..
... CMC experience or equivalent in pharmaceutical development, manufacturing, and/or testing of pharmaceuticals/biologics/medical devices. ... launch market supply of Merck pharmaceutical products worldwide. • Provide regulatory ... understanding of related..
Ensures GxP work is done in compliance with applicable laws, regulations and guidelines
Works closely with internal and external QA and CMC, Clinical and Non-clinical colleagues through all phases ..
Scientist, Analytical Chemistry
Responsible for references standard management, review data from contract service providers (CSP), help with trouble shooting and investigation, assisting in routine and non-routine sample analysis for drug substance ..
Job Description PURPOSE Electronic Document Management Systems Coordinator supporting CGTDM Documentation/QMS organization in the life cycle management of various GxP documents including SOPs, testing monographs, specifications, plans, etc. Supporting the implementation ..
... position is for a leading pharmaceutical company. Below are the details ... APC and IIoT solutions/capabilities in manufacturing settings to achieve actionable insights ... and enable continued improvement for..
10 month contract position with additional opportunity based upon performance and continued business need*
BS degree in Biological Sciences, Chemical Engineering, Biological Engineering, Biochemistry, or related ..
Global Internal Audit & Assurance (GIA) is recruiting the best talent to execute a dynamic risk-based audit plan that identifies value-added recommendations to enhance Company processes and controls. The Senior Auditor ..
Engineer-Validation Technical Services FDE
State / Province
At Lilly, we unite caring with discovery ..
... validation practices across the pharma manufacturing network are in line with ... role in the Pharma MS&T (Manufacturing Science & Technology) team for ... and revalidation/qualification activities for our..
... ID 45836 Title Research Scientist-Technical Services/Manufacturing Science (TS/MS) Molecule Steward City ... will interact with the engineering, manufacturing, validation, quality assurance, quality control, ... support systems used in the..
... combination product scale-up, design for manufacturing, commercialization, operations support, and materials/components ... of automated assembly systems for pharmaceutical and medical industries is preferred ... platforms for testing and pilot..
Your Responsibilities : GSK are seeking a Clinical Safety Scientist to join our busy and talented team. You will be responsible for the continued safety assessment, evaluation and risk management of ..
... for formulation development and GMP manufacturing of oral and injectable dosage ... and excipients), REXIM® (nutraceutical and pharmaceutical amino acids), generic APIs, generic ... generic APIs, generic packages, and..