Title:
Process Quality Excellence Specialist Company:
Global Biotechnology Location:
Slough (Hybrid - 1 day on-site) Planet Pharma is partnered with a global biotechnology company specializing in the research and development of innovative medicines for patients with severe diseases, mainly focusing on neurology and immunology, including areas such as epilepsy, Crohn's disease, and rheumatoid arthritis. Main Responsibilities: Responsible for writing SOPs and managing training assignments. Supporting the management of quality and compliance processes training for the GCSO (Global Clinical Sciences and Operations) group. Providing training when needed and assessing the necessity of new training for certain teams. Conducting GAP analysis by reviewing new regulations and their impact on current SOPs, and creating SOP revisions based on identified gaps. Main Requirements: Previous experience as a clinical quality professional with a strong GCP background. Experience in GCP clinical trials or GCP audit and inspection. Familiarity with systems such as Veeva Vault and Veeva TMF is a plus. Interested?
Apply now for immediate consideration or contact Maria Tsalpatourou at
mtsalpatourou@planet-pharma.co.uk . Seniority Level:
Mid-Senior level Employment Type:
Full-time Job Function:
Quality Assurance Industries:
Pharmaceutical Manufacturing and Biotechnology Research We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation, or age.
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Process Quality Excellence Specialist Company:
Global Biotechnology Location:
Slough (Hybrid - 1 day on-site) Planet Pharma is partnered with a global biotechnology company specializing in the research and development of innovative medicines for patients with severe diseases, mainly focusing on neurology and immunology, including areas such as epilepsy, Crohn's disease, and rheumatoid arthritis. Main Responsibilities: Responsible for writing SOPs and managing training assignments. Supporting the management of quality and compliance processes training for the GCSO (Global Clinical Sciences and Operations) group. Providing training when needed and assessing the necessity of new training for certain teams. Conducting GAP analysis by reviewing new regulations and their impact on current SOPs, and creating SOP revisions based on identified gaps. Main Requirements: Previous experience as a clinical quality professional with a strong GCP background. Experience in GCP clinical trials or GCP audit and inspection. Familiarity with systems such as Veeva Vault and Veeva TMF is a plus. Interested?
Apply now for immediate consideration or contact Maria Tsalpatourou at
mtsalpatourou@planet-pharma.co.uk . Seniority Level:
Mid-Senior level Employment Type:
Full-time Job Function:
Quality Assurance Industries:
Pharmaceutical Manufacturing and Biotechnology Research We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation, or age.
#J-18808-Ljbffr
