Senior Analytical Scientist - Pharmaceutical Development Senior Analytical Scientist - Pharmace[...]

Seeds Renewables; Groton (CT); On-site; USD 110,000 - 140,000; Full time

Job summary

A leading pharmaceutical firm in Groton is seeking a Senior Analytical Scientist. The ideal candidate will design and manage analytical methods to support process development, ensuring high-quality data generation. Responsibilities include overseeing analytical studies, managing stability studies, and collaborating cross-functionally. Candidates should have extensive hands-on experience with HPLC/UPLC and familiarity with various analytical techniques.

Qualifications

• Extensive hands-on experience with HPLC/UPLC, dissolution testing.
• Familiarity with a broad range of analytical techniques.
• Proficiency in analytical instrumentation.

Responsibilities

• Design and manage analytical approaches for process development.
• Oversee analytic studies in a collaborative environment.
• Lead development and validation of robust analytical methods.
• Manage stability studies for establishing shelf-life parameters.
• Collaborate to identify optimal analytical techniques.
• Contribute to regulatory submissions by authoring quality modules.
• Evaluate scientific data to draw clear conclusions, guide future work, and communicate findings through presentations and reports.
• Contribute to regulatory submissions by authoring relevant sections of quality modules, ensuring alignment with global standards.
• Maintain compliance with GLP/GMP standards and safety protocols.

Skills

HPLC/UPLC

Dissolution testing

Analytical techniques

Data visualization

Troubleshooting

GLP/GMP compliance

Tools

SFC

ICP‑MS

UV

Job description

Senior Analytical Scientist - Pharmaceutical Development

Eurofins

Job Description

• Design and manage analytical approaches to support process development, with a focus on chromatographic and dissolution-based methods.
• Oversee and review the planning, development, execution, and interpretation of analytical studies performed by other scientists in a collaborative, matrixed environment.
• Lead the development, validation, and transfer of robust analytical methods, ensuring high-quality data generation and reproducibility.
• Manage stability studies to assess degradation pathways and establish shelf-life parameters.
• Develop impurity control strategies to ensure product quality and regulatory compliance.
• Collaborate cross-functionally to identify and apply optimal analytical techniques, including computational modeling, predictive tools, and data visualization platforms.
• Evaluate scientific data to draw clear conclusions, guide future work, and communicate findings through presentations, technical reports, and other media.
• Contribute to regulatory submissions by authoring relevant sections of the quality modules, ensuring alignment with global standards.
• Maintain compliance with GLP/GMP standards and safety protocols.

Technical Expertise:

• Extensive hands‑on experience with HPLC/UPLC, dissolution testing, and data review in a pharmaceutical R&D setting.
• Familiarity with a broad range of analytical techniques, including SFC, disintegrations, compendial testing (e.g., excipients, packaging release testing), generic testing (e.g., UV, ICP‑MS, titrations)
• Proficiency in analytical instrumentation and troubleshooting