9 qa English-speaking jobs in Parma

are looking forThis is what you will doEnsure the GCP compliance within the project teams, acting as QA ... GCP deviations.Writing the SOPs and working instructions related to the activities performed by R&D QA ... reference person in the clinical project teams, both related to organic and inorganic growth, providing QA ... with the current regulations.You will need to havePreferably: At least 3 years' experience as clinical QA ... implementation and maintenance of the quality system in the GCP areas.You will be responsible forActing as QA

Manage training and documentation across Global TechOps & Supply. Responsibilities include EDMS management, user training, compliance monitoring, and supporting system implementation. Requires a scientific degree and 5+ years in pharma QA.

when delegated.Performing Responsible Person responsibilities when required.Deputizing for the GDP QA ... external partners.This is what you will doWe are seeking an experienced and highly motivated Senior GDP QA ... Practice (GDP) Quality Management System within a dynamic pharmaceutical environment.Reporting to the GDP QA

Pharmacy, Biology, Medicine, Biotechnology, Chemistry or equivalent)3–5 years in pharmacovigilance and/or QA

Pharmacy, Biology, Medicine, Biotechnology, Chemistry or equivalent)3–5 years in pharmacovigilance and/or QA

GCP Specialist in R&D Auditing manages GCP CAPAs, quality metrics, and executes first and second party audits. Requires 3+ years in Pharma/CRO QA with strong GCP knowledge.

implementation of the new document management systemSupervising and supporting the management of the TechOps QA

Toronto (Canada) and Shanghai (China).Who we are looking forThis is what you will doThe Global R&D QA

and re-negotiations or terminations are initiated and completed in a timely fashionLiaise with R&D PV QA