Job Location : Bangalore, Chennai

Experience : 6 Yr

CTC Budget : 1500000 to 2500000

Posted At : 11-Oct-2025

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We are seeking an experienced Documentum Developer with a strong background in supporting validated systems within the Life Sciences or Pharmaceutical industry.
The ideal candidate will have hands-on experience with Documentum (v7.1 and above), including development, upgrade, migration, and production support, with a focus on compliance and quality processes.

Key Responsibilities:
• Lead or support development, upgrade, migration, and production support activities in OpenText Documentum environments (v7.1 and above).
• Work extensively with Documentum modules such as WebTop, WDK, D2, XCP, and DFC.
• Configure and customize EMC Documentum D2-Client and D2-Config, including installation and integration.
• Monitor and troubleshoot Documentum services on UNIX platforms, including log file analysis and root cause investigation.
• Develop and optimize DQL (Documentum Query Language) queries and custom APIs using Java/J2EE and DFC.
• Collaborate with Quality Assurance and Validation teams to ensure regulatory compliance (21 CFR Part 11).
• Provide support for compliance-related activities including periodic reviews, deviation assessments, CAPA root cause analysis, and technical documentation.
• Utilize tools such as Documentum Composer, DAR Installer, BPM, Documentum Administrator, xPlore, and Adlib for system configurations and maintenance.
• Participate in requirement analysis, design reviews, and solution implementation based on business needs.

Required Skills & Experience:
• 6+ years of recent hands-on experience with Documentum (v7.1 or higher).
• Expertise in Documentum technologies including DFC, DQL, API, CTS, WebTop, WDK, D2, XCP.
• Strong programming knowledge in Java/J2EE and scripting languages.
• Solid experience with UNIX environments for monitoring and troubleshooting.
• Proficient with application servers such as Tomcat, JBoss/WildFly.
• Familiarity with relational databases (e.g., SQL Server), DQL, and SQL.
• In-depth experience with validated systems and compliance frameworks (21 CFR Part 11).
• Domain experience in Life Sciences, particularly in Quality and Manufacturing.
• Experience with the Documentum product suite upgrade (Content Server, Repository, xPlore, CTS, DARs).
• Working knowledge of Web Services (REST/WSDL) integrations.

Preferred Qualifications:
• Experience with LSQM (Life Sciences Quality Management) solutions.
• Strong understanding of pharmaceutical compliance requirements and documentation standards.
• Familiarity with Adlib configuration and administration.