Pharmacovigilance Quality Specialist – Immediate Start
Our Client a leading global Pharmaceutical Company has a vacancy for a Pharmacovigilance Quality Specialist contractor within their Safety department. Within this role you will be responsible for supporting functions with PV business process development and corresponding documentation. This role includes working on various topics and process improvement teams with the purpose of providing advice on documentation matters Collaborate with Business Process Owners (mainly Safety department) and facilitate the development of PV Standard Operating Procedures (SOPs) Provide guidance on PV SOPs (content, quality, document lifecycle) Conduct process-mapping sessions Write and review SOPs The ideal candidate will possess a BSc or equivalent in relevant scientific discipline and relevant pharmaceutical experience; excellent attention to detail is a must. You will have experience in Pharmacovigilance e.g. Safety Compliance, Safety Operations, this is essential. Experience in quality or process management and SOP writing is a must. For further information please call Roberta on 0203 465 0044 or email firstname.lastname@example.org
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