Mass Spec Bioanalytical Scientist

~ Full time on-site role in Rockville, MD ~

You will develop and validate bioanalytical methods to support the pipeline of biologic therapies.

You will serve as the LCMS expert.

You will make an impact on new and existing products. 

Key Responsibilities:

1. Serve as the lead Scientist for non-GLP, as well as GLP and GCP bioanalytical studies.
2. Develop and validate robust bioanalytical methods, and troubleshoot and resolve issues.
3. Interpret, analyze, and report analytical results for method development and validation.
4. Prepare and review study protocols, analytical procedures, and reports for regulatory submissions.
5. Ensure the quality and integrity of the studies.
6. Identify and help implement process improvements.
7. Mentor new employees and develop training materials and schedules.
8. Stay current on new methodologies and techniques. 

Experience:

• 2-5 years of industry experience with PhD or 5+ years of relevant experience with MS.
• Hands-on experience with ligand binding assays or qPCR methods.
• Planning and executing experiments to support research activities and project goals.
• Develop a wide range of methodologies and ability to recommend alternatives.
• Analysis and resolution of problems and experience troubleshooting assays.
• Statistical analysis, data interpretation, and recommendations for next steps.

Qualifications:

• Solid understanding of Mass Spec platforms.
• Relevant bioanalytical FDA guidance documents and expectations of bioanalytical assays.
• Exceptional oral and written communication skills, coupled with project leadership.

 Additional Points:

-- This is a full time onsite role in Rockville, Maryland.

-- Competitive compensation package includes base salary of $125-150k plus bonus.

-- Comprehensive relocation package available.