Veeva QMS Lead

Job Title

Required Skills:

• IT Manufacturing Domain (Qualification implementation and Advisory in Veeva QMS)
• Minimum 6 years of IT experience in pharma domain for implementing and managing Veeva QMS.
• Minimum of Bachelor's Degree or applicable experience within information/Computer systems with focus on Qualification of Mfg. applications
• Must have experience on implementation, consulting for Veeva QMS in Life Sciences.
• Deep knowledge of Veeva QMS, Veeva Vault configuration, developing them in live projects based on client requirement.
• Previous experience in the biotechnology / Pharmaceutical / Life Science or related industry implementing and validating computer systems that manage regulated information
• Working knowledge of IT infrastructure qualification processes and IT operating procedures
• Thoroughly familiar with Quality GxP IT compliance requirements.
• Strong planning and analytical skills combined with ability to work with geographically distributed teams in a rapid development model.
• Awareness of ITIL and Support Project Methodology.
• Ability to familiarize himself / herself independently with entirely new subjects and thus provide comprehensive and innovative solutions
• Excellent written and verbal communications skills
• Solid grasp of Information security and standard methodologies
• Working knowledge of Document and Object record migration from legacy application to Veeva Vault.
• Good technical knowledge in core technologies and platforms such as Java,.Net, XML, HTML, PL/SQL API.
• In-depth knowledge of quality management principles and industry regulations (e.g., FDA, ISO).
• Qualified on Global Quality tracking systems for initiation handling and closure of investigation