Veeva Consultant

• 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: