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Job in Regulatory Affairs as Analyst at Merck

 

Clinical courses

 

Clinical research courses

Merck is an ongoing journey of discovery: our 50,000 people are shaping how the world lives, works and plays through next generation advancements in healthcare, life science and performance materials. For 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others.

Post : Healthcare R&D IT System Analyst - Regulatory Affairs

Job Description
• Maintain and troubleshoot our applications, respond to support requests from users
• Impacts the results within own discipline with own contributions. Provides input to the technical direction and operational decision making in the field of specialization.
• Prepares communications and makes presentations on system enhancements and/or alternatives. Evaluates, optimizes, harmonizes and standardizes existing systems.
• Oversees system documentation. Monitors quality standards and ensures failure-free operation. Considers compatibility of different systems.
• Solves a range of straightforward problems through knowledge and technical experience in own discipline with a moderate level of guidance.
• Analyzes factual information and possible solutions and makes independent judgments, decisions and recommendations.
• Understands how the team integrates with other teams in order to achieve overall objectives of the area and builds knowledge of the organization, processes, customers and key business drivers.

Candidate Profile
• Minimum of 3-6 years of experience
• Minimum of Associates Degree or applicable experience within information systems
• Service Delivery Management mindset
• Ability to familiarize himself / herself independently with entirely new subjects and thus provide comprehensive and innovative solutions
• Excellent written and verbal communications skills
• Working knowledge of information security and best practices
• Solid background & knowledge in computer infrastructure from the desktop to the data source
• Good technical knowledge in core technologies and platforms such as Java, Citrix, Windows, Linux, Scripting, Java, XML, HTML, Oracle SQL & PL/SQL
• Proven fast learning & problem management skills
• Proven experience of working under pressure
• Thoroughly familiar with Quality & GxP IT compliance requirements
• Good customer service skills

Additional Information:
Qualification : Associates Degree
Industry Type: Pharma/ Biotech/Clinical Research
Location: Karnataka - Bangalore
Functional Area: Regulatory Affairs

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