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C

Product Specialist

5-10 Years
28 - 30 LPA
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Job Description

Key Skills:GxP Validation Practices, GxP compliance, Validation, LIMS (Laboratory Information Mangement System), LabVantage SDMS handler

Roles and Responsibilities:

  • Conduct validation activities for laboratory systems, ensuring compliance with GxP standards.
  • Manage and maintain Laboratory Information Management Systems (LIMS) to support laboratory operations.
  • Implement and oversee GxP validation practices across various projects.
  • Collaborate with cross-functional teams to ensure adherence to regulatory requirements.
  • Provide training and support to staff on validation processes and compliance standards.
  • Assist in the development and review of validation documentation.

Skills Required:

  • Strong understanding of GxP validation practices and regulatory compliance in pharmaceutical/biotech environments
  • Hands-on experience with LIMS systems for managing laboratory workflows and data
  • Ability to implement and oversee validation activities across multiple projects
  • Familiarity with LabVantage SDMS for sample and data management (nice-to-have)
  • Expertise in creating, reviewing, and maintaining validation documentation
  • Strong analytical and problem-solving skills for troubleshooting validation issues
  • Excellent communication and collaboration skills for working with cross-functional teams
  • Knowledge of industry regulations, quality standards, and best practices

Education:Any Graduation, Any Post Graduation

Any Graduate

More Info

Job Type:
Function:
Employment Type:
Open to candidates from:
Indian

Job ID: 145017229