About the role
AI summarisedThe Validation Scientist II role at Thermo Fisher Scientific involves designing and executing experiments, analyzing data, and contributing to product and process development within a research and development environment. The position supports the development and optimization of scientific solutions with real-world impact in healthcare and related fields. It requires strong technical, analytical, and communication skills, along with the ability to work independently and collaboratively in a regulated setting.
Life SciencesOnsite
Key Responsibilities
- Contribute to continuous improvement initiatives
- Develop and optimize products and processes
- Independently plan the best scientific approach to develop analytical methods and/or other specialty technologies studies that meet client requirements
- Evaluate available technical options to obtain desired quality of analytical results, economics, ease of introduction into a production environment, and robustness in analytical applications
- Demonstrate viability of in-house developed methods and methods transferred from clients by designing appropriate validation experiments or other appropriate aspects of specialty methodology or technology
- Review protocols, project status reports, final study reports and other project-related technical documents
Requirements
- Advanced Degree with no prior experience required, or bachelor's degree plus 2 years of relevant industry or research experience
- Preferred Fields of Study: Chemistry, Molecular Biology, Biochemistry
- Strong technical expertise in laboratory techniques and instrumentation specific to role
- Proven ability to design, execute and analyze complex experiments independently
- Experience with data analysis, documentation and technical writing
- Strong project management and organizational skills
- Excellent problem-solving and troubleshooting abilities
- Proficiency with relevant software and data analysis tools
- Strong communication and interpersonal skills
- Demonstrated ability to work both independently and collaboratively
- Experience with quality systems (GCP, GLP, ISO) preferred
- Ability to adapt to shifting priorities
- Knowledge of applicable regulatory requirements and safety protocols