Data Validation, Analyst I

Thermo Fisher Scientific

Thermo Fisher Scientific offers a dynamic role for a Data Validation Analyst I within a team-focused environment. This position is essential for contributing to project directions, reviewing change requests, and ensuring testing accuracy. The role supports new releases and modifications to applications in alignment with the company's quality standards. The ideal candidate will join a team dedicated to ensuring effective system management and user support during implementation and ongoing use.

In this role you can expect to have the responsibilities:

• Contribute to project teams to enhance system operations and ensure communication accuracy in testing.
• Provide validation support for new releases and modifications throughout software development.
• Draft and manage documents like Change Controls, VDA, IQ, OQ per SOP for GMP systems.
• Oversee vendor installations on validated GMP hardware and software systems.
• Complete IQ, OQ documentation for validated GMP systems according to SOP.
• Support users by providing training and maintenance for validated platforms.

This role comes with the following benefits:

This role requires you to have:

• Bachelor’s degree or equivalent academic/vocational qualification.
• Entry-level to 2 years of experience in Validation Analyst roles with GMP exposure.
• Experience leading vendor activities on-site.
• Strong analytical skills and attention to detail.
• Ability to work in a team-oriented environment.
• Proficient in written and verbal communication.
• Proficiency in Microsoft Office Suite and data analysis tools.
• Ability to adhere to deadlines and manage multiple tasks.

You would benefit from having:

This role requires adherence to GMP Safety Standards and may involve wearing PPE such as safety glasses and lab coats. The work setting varies between laboratories and office environments.