Job Description
Title: Process Quality Excellence Specialist
Company: Global Biotechnology
Location: Slough (Hybrid - 1 day on-site)
The global biotechnology company, specializing in research and development of innovative medicines for patients with severe diseases, focuses on neurology and immunology.
Main Responsibilities
* Write SOPs and manage training assignments
* Support the management of quality and compliance processes training for the GCSO group
* Provide training when needed and check for new training requirements or applicability to certain teams
* Perform GAP analysis for new regulations and their impact on current SOPs, creating revisions based on identified gaps
Main Requirements:
* Clinical quality professional experience with a strong GCP background
* GCP clinical trials or GCP audit and inspection experience
* Veeva Vault and Veeva TMF system experience is a plus
About {company}
{company} provides global staffing services, investing in an international platform to work compliantly in 30+ countries. Our network includes 2500+ active contractors globally and a strong permanent/direct hire recruitment offering. We offer specialist knowledge, close relationships with clients and industry expertise in Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing.
We are an equal opportunities Recruitment Business and Agency.
We welcome applications from all suitably qualified candidates regardless of race, sex, disability, religion/belief, sexual orientation or age.
www.{company}.com