RemoteOtterRemoteOtterExplore 15 Remote Glp Jobs
T.G.F
The Geneva Foundation
The Clinical Research Coordinator I manages research studies and coordinates activities at the Naval Medical Center in Portsmouth, VA.
T.G.F
The Geneva Foundation
The Research Coordinator will assist in coordinating research activities, including participant recruitment and data management, for a project focused on chronic pain management.
Amgen
Amgen is seeking a Director for Small Molecule Process Development to lead a team in developing drug manufacturing processes and ensuring regulatory compliance.
Eurofins
The Extractables and Leachables Principal Scientist is responsible for conducting analytical tasks and developing methods for drug product testing.
Lifelancer
The Analytical Method Validation Associate supports clients in developing and validating analytical methods for cleaning validation activities.
A.B.S.C
Advanced Bio-Logic Solutions Corp
The Quality Assurance Manager oversees quality assurance processes for computerized systems, ensuring compliance with regulations and leading initiatives for quality improvement.
Cerba Research
Join Cerba Research as a Quality Assurance Manager to ensure regulatory compliance and high-quality standards in a clinical laboratory setting.
D.M
Disc Medicine
Disc Medicine is seeking an Associate Director for Quality Assurance Vendor Management to oversee GxP audits and vendor management in a hybrid work environment.
Nurix
Nurix
Nurix Therapeutics is seeking a Toxicology Scientist to lead and manage safety pharmacology and toxicology studies in drug development.
T.P.A
Telix Pharmaceuticals (Americas)
Join Telix Pharmaceuticals as a Scientist II in the radiochemistry laboratory, focusing on the development and optimization of radiopharmaceutical production processes.
Pharma Universe
Join the Quality Control team as a Chemist II/III, performing analytical testing in a GMP/GLP-regulated environment.
A.B.S.C
Advanced Bio-Logic Solutions Corp
Seeking a Quality Assurance Specialist with Computer Systems Validation experience for a contract role.
Santen
Join Santen as a Non-Clinical Audit Specialist to ensure quality and reliability in pharmaceutical operations.
SGS
The Business IT manager – CSV will lead the IT team and manage validation projects in a GMP environment.
wega Informatik AG
The Lab Automation Consultant will support the implementation and maintenance of lab automation systems in a dynamic Pharma and Life Science IT service provider.