
Validation Specialist Trainee
- Verna, Goa
- Permanent
- Full-time
- Develop and maintain standardized validation templates for internal use and for clients that comply with industry standards and regulatory guidelines, such as Good Automated Manufacturing Practice (GAMP), FDA 21 CFR Part 11, and EU Annex 11.
- Review and understand system updates, including new releases and hotfixes, to determine the impact on validation documents.
- Generate validation documents for clients based on the functional and design specifications of the projects.
- Execute internal validation protocols as needed to ensure system functionality.
- Act as a resource person at the documentary level (URS, FS, DS, Test plan, etc. )
- Provide Necessary Change Control Documents as per customer requirements.
- Author Factory Acceptance test, Site Acceptance Test documents.
- Support internal Teams and customer on Queries related to Validation documents
- Author and support Onsite Qualification Documents such as IOQ, Trace matrix etc.
- Identify potential risks associated with validation activities and develop mitigation strategies.
- Lead root cause investigations for validation discrepancies and implement corrective actions for continuous quality improvement.
- Collaborate closely with the internal team and clients to provide expert guidance on validation strategies and best practices.
- Work closely with the quality assurance (QA) team to ensure that validation activities are in line with internal quality systems and external regulatory requirements.
- Partner with various internal departments to deliver validation documentation at specific stages of project development.
- Perform any other tasks related to validation processes.
- College diploma in a relevant field.
- Excellent proficiency in English (written and spoken).
- Advanced knowledge of the Microsoft Office suite.