Scientist, Pharmaceutical Science​/ Research

Job Title:

Analytical Development Scientist

Job Description

This role focuses on supporting process development teams through advanced analytical testing and assay development in a fast-paced laboratory environment. The scientist performs complex analytical methods, generates and interprets data, troubleshoots issues, and ensures that results reliably support product development and GMP manufacturing decisions for vaccine and therapeutic products.

Responsibilities

+ Perform analytical assay development and characterization work to support vaccine and therapeutic product programs.

+ Support process development efforts by designing, executing, and refining analytical testing strategies.

+ Develop, optimize, and qualify analytical testing methods to ensure robust, reproducible data.

+ Run complex liquid chromatography and related analytical techniques, including HPLC, UPLC, reverse phase chromatography, size exclusion chromatography (SEC), lipid content analysis, and mass spectrometry (MS) where applicable.

+ Support formulation development and characterization activities by providing analytical data and method expertise.

+ Conduct GMP testing and lot release testing in accordance with established quality and regulatory standards.

+ Analyze data, interpret results, and troubleshoot analytical issues to resolve problems and improve methods.

+ Prepare and maintain clear, accurate technical reports, protocols, and GMP documentation.

+ Present analytical findings and recommendations to cross-functional teams in a clear and concise manner.

+ Collaborate closely with Process Development, Quality, Manufacturing, and Operations teams to align analytical strategies with development and production needs.

+ Work independently in the laboratory while managing a high volume of testing and supporting multiple internal functions simultaneously.

+ Ensure all laboratory activities adhere to applicable procedures, quality standards, and regulatory expectations.

Essential Skills

+ Bachelor's degree in a scientific discipline such as Biology, Biochemistry, Chemistry, Pharmaceutical Sciences, Engineering, or a related field.

+ At least 6 years of experience as an Analytical Development Scientist.

+ At least 6 years of experience developing and executing liquid chromatography methods, including reverse phase chromatography, size exclusion chromatography (SEC), and lipid content analysis.

+

Demonstrated proficiency in analytical method development, optimization, and qualification.

+ Strong analytical problem-solving abilities and experience troubleshooting complex assays.

+ Proven ability to work independently in a laboratory setting while managing a high testing volume.

+ Proficiency with Microsoft Office applications, including Outlook, Word, Excel, and PowerPoint.

+ Experience supporting process development activities through analytical testing in a biopharmaceutical or related environment.

Additional

Skills & Qualifications

+ GMP experience, including GMP testing and lot release testing.

+ Hands-on experience with mass spectrometry (MS) techniques.

+ Formulation development and characterization experience.

+ Prior experience in biologics, vaccines, cell therapy, gene therapy, or pharmaceutical product development.

+ Background in analytical development within a biopharmaceutical, vaccine, or advanced therapeutics environment.

+ Experience supporting process development in a regulated setting.

+ Knowledge of federal compliance and sponsored project management gained through exposure to complex research programs.

+ Interest in mission-driven science focused on next-generation vaccines and emerging cancer vaccine platforms.

+ Motivation to grow through structured training, certifications, and professional development opportunities.

+ Ability to thrive in a collaborative, high-performing culture that values communication and shared problem-solving.

Work Environment

The position is based in a fast-paced GMP testing laboratory operating Monday through Friday from 8:00 AM to 5:00 PM. The environment centers on high-complexity analytical work supporting vaccine and therapeutic product development, with extensive use of HPLC, UPLC, reverse phase and…