Associate Research Scientist

Thermo Fisher Scientific - Richmond, VA

Full-time - Mid Level

Richmond, VA

Computer and Electronic Product Manufacturing

About the position

The Associate Research Scientist at Thermo Fisher Scientific plays a crucial role in the regulatory and scientific conduct of various development and validation projects, particularly in the context of clinical trials. This position involves performing analytical testing, method optimization, and troubleshooting on multiple analytical instruments, ensuring compliance with Good Manufacturing Practices (GMP) and other relevant standards. The role requires strong project management skills and the ability to communicate effectively with clients and team members, contributing to the overall mission of improving health outcomes through scientific innovation.

Responsibilities

• Responsible for the regulatory and scientific conduct of development, validation, and stability projects.
• Perform troubleshooting on multiple analytical instrumentation and detection techniques.
• Calculate and interpret data, recording it in adherence with PPD SOPs and client requirements.
• Act as the technical project leader for multiple projects, providing updates to clients as needed.
• Independently perform analytical testing and method optimization/validation for pharmaceutical compounds.
• Design and implement experiments independently, reviewing and critiquing study protocols and reports.
• Prepare and review project-related technical documents, including study protocols and final reports.
• Communicate data and technical issues to clients on a weekly basis or as needed.
• Provide technical guidance and training to staff, leading troubleshooting sessions.
• Assist in the preparation and implementation of SOPs and quality systems.

Requirements

• Bachelor's degree or equivalent in a relevant field.
• 5+ years of experience in a related role, with knowledge of GMP and GLP.
• Proficiency in analytical instrumentation such as HPLC, GC, UPLC, ICP-MS, and LC/MS.
• Strong technical writing skills and experience in project management.
• Ability to perform root cause analysis and troubleshoot effectively.
• Good written and oral communication skills, with the ability to work collaboratively.

Nice-to-haves

• Experience in clinical trials and regulatory compliance.
• Familiarity with laboratory safety protocols and hazardous materials handling.

Benefits

• Health insurance coverage
• 401k retirement savings plan
• Paid time off and holidays
• Professional development opportunities
• Flexible scheduling options