Duties/responsibilities:
·Will be working on procedural documents via Mastercontrol system and Viva
·Will be working on harmonizing effort- someone who will oversee the harmonization process
·A good Project Manager
·Will be starting the QMS
·Ability to work cross-functional and cross-developmental, someone who can work really well with vendors and clients
Qualifications:
·Knowledge of
·Knowledge of LMS
·Strong Project Management skills
·Pharmaceutical experience- must have
·Background in Clinical trial work and R&D
·Global harmonization process experience- nice to have
·Someone who has experience with SOP- must have
·Previous SOP harmonization experience- nice to have
· Not looking for someone who has manufacturing background
·PMP certification is not required