Explore 20 Remote Gmp Compliance Jobs
A.T
Akero Therapeutics
The Manager of Quality Assurance will oversee quality compliance for outsourced biologics programs, ensuring adherence to regulatory standards.
S.B.G
Syner-G BioPharma Group
Seeking a Senior Project Manager to lead large-scale capital projects in biologics manufacturing.
B.D.A.C
Becton, Dickinson and Company
The Molding Maintenance Technician 2 is responsible for maintaining and troubleshooting complex manufacturing equipment to ensure optimal production and quality.
Lead quality oversight for Amgen's contract manufacturing locations in Japan, ensuring compliance with GMP standards and driving continuous improvement.
U.L.H
US05 Lonza Houston
The Director of Project Delivery UK oversees investment projects in the pharmaceutical sector, ensuring compliance and effective project management.
The Scientific Writer will perform data reviews, create documentation, and coordinate communication for CAR-T particulate matter investigations.
Lead quality oversight for global suppliers as a Quality Senior Manager at Amgen.
Join Syner-G BioPharma Group as a Sr. Project Manager to lead capital projects in biologics manufacturing.
Join Nutrafol as a Quality Assurance Associate to ensure compliance and support growth in the dietary supplement industry.
B.U
BeiGene UK
The Manager of Global QC at BeOne Medicines Ltd. oversees quality control and analytical development activities at Contract Manufacturing Organizations, ensuring compliance and supporting global product launches.
Join AbbVie as a Principal Auditor to lead compliance audits and ensure quality standards in the pharmaceutical industry.
Davol
Davol
The Mold Utility Operator is responsible for producing quality syringes while ensuring compliance with safety and quality standards.
The Senior Associate Manufacturing role focuses on driving process efficiencies and managing strategic projects in biopharmaceutical manufacturing.
The Stationary Engineer is responsible for maintaining and troubleshooting utility systems in a GMP environment.
The Qualified Person is responsible for batch release and certification, ensuring compliance with GMP standards.