Veeva Consultant

1 week ago


Hyderabad India Infosys Limited Full time

Job Description Job Description: - Senior Consultant Pharmaceutical QMS GxP - We are seeking a highly experienced IT Consultant 10 years to lead the design and implementation of Quality Management Systems QMS in GxP regulated pharmaceutical environments - This role combines deep expertise in business analysis and eQMS implementation with strong advisory capabilities in process harmonization and regulatory compliance - As a key member of our Life Sciences R D consulting team you will play a pivotal role in delivering scalable compliant QMS solutions - You ll lead quality initiatives facilitate cross functional workshops and help shape global quality processes aligned with regulatory standards such as ICH FDA EMA MHRA and ISO 9001 Key Responsibilities: - Lead workshops to assess current QMS maturity and define future state processes - Design scalable GxP compliant QMS frameworks tailored to client needs - Collaborate with cross functional teams to gather and document requirements across functional migration and integration workstreams - Translate business needs into functional specifications using tools like JIRA and HP ALM - Implement and support supplier qualification audits performance monitoring and risk management processes - Integrate supplier quality workflows into enterprise QMS platforms - Lead workshops to assess current QMS maturity and define future state processes - Design scalable GxP compliant QMS frameworks tailored to client needs - Collaborate with cross functional teams to gather and document requirements across functional migration and integration workstreams - Translate business needs into functional specifications using tools like JIRA and HP ALM - Implement and support supplier qualification audits performance monitoring and risk management processes - Integrate supplier quality workflows into enterprise QMS platforms Technical Requirements: - Proven experience in eQMS design and implementation within GxP regulated environments - In depth knowledge of QMS processes such as supplier quality audit processes risk management change control deviation complaints etc - Hands on experience with leading QMS tools such as Veeva Vault TrackWise TrackWise Digital ETQ Reliance and MasterControl - Strong background in business analysis stakeholder engagement and regulatory compliance - Excellent communication facilitation and project management skills - Ability to work both independently and collaboratively across global teams Additional Responsibilities: - A degree in a technical scientific or clinical discipline is preferred Preferred Skills: Technology->Life Sciences->CTMS/Trial conduct->Veeva Vault



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