Eurofins Lancaster Laboratories

Pharmaceutical Materials Scientist-API & Small Molecule Development

Eurofins Lancaster Laboratories • $80K — $95K *
Groton, CT 06340In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
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Job Overview by Ladders

Qualifications

  • Bachelor's in Pharmaceutical Sciences, Chemistry, Chemical Engineering, Materials Science, or related field; 2+ years experience or Master's degree.
  • Hands-on experience in pharmaceutical, API, and small molecule testing.
  • Strong knowledge of solid-state characterization techniques like XRPD, DSC, TGA, FTIR, and Raman.
  • Proficiency in data analysis and problem-solving in solid-state chemistry and particle characterization.
  • Good understanding of physical, analytical, and organic chemistry principles.
  • Strong organizational, communication, and collaboration skills.

Responsibilities

  • Perform solid-state characterization of pharmaceutical small molecules using advanced techniques.
  • Execute polymorph, salt, co-crystal, and crystallization screening studies for API development.
  • Conduct detailed particle and powder characterization analysis.
  • Collaborate with teams in Medicinal Chemistry and Formulation Development for solid-form selection.
  • Analyze experimental data, troubleshoot challenges, and give technical recommendations.
  • Maintain accurate documentation in electronic lab notebooks.
  • Contribute to innovative approaches in materials science and improvement initiatives.

Benefits

  • Comprehensive medical coverage with dental and vision options.
  • Life and disability insurance.
  • 401(k) plan with company match.
  • Paid vacation and holidays.
Full Job Description
Job Description

We are seeking a Materials Scientist with hands-on experience in pharmaceuticals, API (Active Pharmaceutical Ingredient), and small molecule testing for drug production to support drug development programs through advanced solid-state and particle characterization.

Key Responsibilities
  • Perform solid-state characterization of pharmaceutical small molecules using techniques such as XRPD, DSC, TGA, microscopy, spectroscopy, and moisture sorption analysis.
  • Execute and support polymorph, salt, co-crystal, and crystallization screening studies for API development projects.
  • Conduct particle and powder characterization, including particle size, shape, surface energy, and surface morphology analysis.
  • Collaborate with cross-functional teams in Medicinal Chemistry, Formulation Development, Biopharmaceutics, and Materials Science to support solid-form selection and clinical development activities.
  • Analyze experimental data, troubleshoot scientific challenges, and provide technical recommendations to project teams.
  • Maintain accurate documentation and data records within electronic laboratory notebook systems.
  • Contribute to innovative materials science approaches and continuous improvement initiatives.


Qualifications
  • Bachelor's degree with 2+ years of industry experience or Master's degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, Materials Science, or a related field.
  • Required: Strong experience in pharmaceutical, API, and small molecule testing supporting drug production and development.
  • Hands-on experience with solid-state characterization techniques including XRPD, PLM, DSC, TGA, FTIR, Raman, and related analytical methods.
  • Strong data analysis, interpretation, and problem-solving skills related to solid-state chemistry, particle characterization, and pharmaceutical materials science.
  • Understanding of physical, analytical, and organic chemistry principles.
  • Excellent communication, organizational, and collaboration skills with the ability to work independently and within multidisciplinary teams.
  • Experience with SSNMR, NIR spectroscopy, or programming/data analysis tools is a plus.
  • Preferred Candidate Profile
  • The ideal candidate is a scientifically curious professional with a passion for pharmaceutical materials characterization, API development, and small molecule drug production, who thrives in a collaborative research environment and enjoys solving complex scientific challenges


Additional Information
  • The position is full-time, M- F 8 am to 5 pm
  • May be requested to work on weekends, overtime, and holidays based on business needs.
  • 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
  • #LI-EB1


About Eurofins Lancaster Laboratories

Eurofins Lancaster Laboratories is a leading contract research organization (CRO) providing analytical, research and testing services to clients in the pharmaceutical, biopharmaceutical, biotechnology, crop protection, chemical, food, environmental and consumer products industries. The company was founded in 1961 and has grown to become one of the largest CROs in the world, with over 50 locations in 20 countries. Eurofins Lancaster Laboratories is part of the Eurofins Scientific Group, a global leader in bioanalytical testing and laboratory services. The company's services include method development and validation, stability testing, quality control testing, and regulatory compliance support.
Learn more about Eurofins Lancaster Laboratories
Size
12,000 employees
Industry
Pharmaceuticals & Biotech
* Ladders Estimates

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