Pharmaceutical Materials Scientist-API & Small Molecule Development

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Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

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

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

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