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Drug Product Analytical Development Scientist

Job in New London, New London County, Connecticut, 06320, USA
Listing for: Eurofins PSS Insourcing Solutions
Full Time position
Listed on 2025-12-02
Job specializations:
  • Science
    Research Scientist, Clinical Research
Salary/Wage Range or Industry Benchmark: 70000 - 80000 USD Yearly USD 70000.00 80000.00 YEAR
Job Description & How to Apply Below

Drug Product Analytical Development Scientist

Base pay range: $70,000.00/yr - $80,000.00/yr

Eurofins Scientific is a leading international life sciences company that delivers a wide range of analytical testing services to clients across multiple industries, ensuring product safety, authenticity, and accurate labeling.

Job Description
  • Design and guide analytical strategies to support manufacturing process development.
  • Lead the planning, development, execution, and data interpretation performed by other scientists in a collaborative, matrixed environment.
  • Oversee and review the development, validation, and transfer of analytical methods to ensure robust and reliable data generation.
  • Manage stability studies to assess degradation pathways and establish shelf-life parameters.
  • Develop impurity control strategies to ensure product quality and regulatory compliance.
  • Experience with a wide range of analytical testing including dissolution, HPLC/UPLC, SFC, disintegration, compendial testing (e.g., excipients/packaging release testing), generic testing (e.g., solvents, water, ash, titrations, heavy metals, ICP/MS, UV) and compound specific methods.
  • Collaborate with cross-functional teams to identify and apply the most effective analytical techniques, including the use of 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 and expectations.
  • Maintain compliance with GLP/GMP standards and safety protocols.
Qualifications
  • PhD in Chemistry, or related field, with 3+ years of pharmaceutical R&D experience or a B.S./M.S. with 15+ years.
  • Strong oral and written communication skills.
  • Experience in a regulated laboratory environment (GLP/GMP).
  • Proven ability to lead scientific projects and mentor team members.
  • Proficiency in analytical instrumentation and techniques.
  • Familiarity with regulatory documentation and submission processes.
Additional Information
  • Position is full-time, Monday-Friday, 8:00 am - 5:00 pm.
  • Candidates currently living within a commutable distance of Groton, CT are encouraged to apply.
  • Excellent full-time benefits including comprehensive medical coverage, dental, and vision options.
  • Life and disability insurance.
  • 401(k) with company match.
  • Paid vacation and holidays.
  • Authorization to work in the United States indefinitely without restriction or sponsorship.

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

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