| Date de publication | Type de poste | Lieu de travail | Expérience | Étude | Disponibilité |
| 17 mars 2022 | Tunis, Tunisie | Entre 1 et 2 ans | Bac + 2 | Plein temps | Français , Anglais |
Description de l’annonce:
MAIN RESPONSIBILITIES
· Prepare CMC regulatory documents within established timelines(Modules2.3&3.2,IMPD,variations)
· Analyzeand/orwritescientificreportsfromtheraw dataprovidedbytheclient.
· Regulatory compliance: comparison of analytical proceduresand/ormanufacturingprocessbetween MAdossierandmanufacturingsiteprocedures.
· Applyinternalprocessesandtemplatesaswellasbest practices of theprofession
· Reportanydeviationorissuetoyourmanagerand proposecorrectiveorpreventiveactions.
· Provideon-goingsupporttotheCMCLeaderandto projectteamstoensurethatprojectobjectivesaremet.
· ContributetodataentryinPLGtoolsenabling measurements ofKPI
· AssistinthepreparationorupdateofStandard Operating Procedures (SOPs) and Working Practice Documents(WPDs)
EDUCATION & EXPERIENCE
u DegreeinlifeScience/Pharmacyrelatedfield
u 0-2yearsofexperienceinCMCand/orQuality AssuranceinPharmaceuticalIndustry
SKILLS
u FluentinEnglish/French(written&spoken)
u Excellent attention todetail
u Abilitytoworkwellwithinateam
u Good time managementskills
u Abilitytoworktotightdeadlines
u Processoriented
u Excellent communicationskills