Contract Jobs

We have a current opportunity for a Regulatory Affairs Specialist on a contract basis. The Regulatory Affairs Consultant will be responsible for providing strategic guidance on regulatory requirements and submissions for medical devices. This role involves ensuring compliance with global regulations, preparing and managing regulatory submissions, a...

We are seeking a highly skilled Computer System Validation (CSV) Engineer to join our client on a contract basis. This role is crucial for ensuring the validation and compliance of computerized systems in a regulated, GxP-compliant environment, contributing to the production of innovative oncology treatments.Key Responsibilities:Lead and Execute CS...

We are seeking a highly skilled QA Supervisor to join a leading Medical Device company. In this role, you will be responsible for:Maintaining a Quality Management System compliant with FDA regulations and driving continuous improvement.Managing complaint handling and adverse event reporting, ensuring that processes, including sterilization, remain ...

EPM Scientific are currently collaborating with a leading Biotechnology Research client who specialise in consulting and clinical development.Our client is seeking a Freelance AMCP Dossier specialist with expertise in the Oncology space, specifically focusing on the US market. Requirements- Must be US based.- Must have AMCP writing experience (US e...

We are seeking an experienced consultant for the validation of fill & finish processes for one of our client. The ideal candidate will have a strong background in the pharmaceutical industry and will ensure that production processes comply with regulatory standards and Good Manufacturing Practices (GMP).Responsibilities:Plan and execute validation ...