Characterization Scientist

Job Description

Job Description

Company Description

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.

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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical, and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences, and in the support of clinical studies.

Join us in shaping a safer, healthier, and more sustainable world. Explore opportunities with Eurofins and be part of a global team driving scientific excellence. Apply today and make a meaningful impact!

The Characterization Scientist will contribute to the formulation and process development of biotherapeutic products. This laboratory-based role is responsible for performing analytical testing and comprehensive characterization of candidate molecules using a range of biophysical, biochemical, and particulate characterization techniques. The position also supports routine laboratory operations and maintenance.

This role supports biotherapeutic products across the development lifecycle, from preclinical and Phase I clinical trials through late-stage development, license application, and commercialization. Additional responsibilities include data compilation, preparation of presentations and reports, and support of departmental documentation.

Responsibilities

Key responsibilities include, but are not limited to:

• Support the development of parenteral formulations for a variety of biotherapeutic modalities, including monoclonal antibodies, antibody–drug conjugates, proteins, mRNA, and vaccines.
• Perform rapid and comprehensive characterization of candidate molecules to assess stability profiles using biophysical, biochemical, and particulate characterization techniques, including:
  • HPLC methods (SE-HPLC, IEX, HIC, RP-HPLC)
  • Capillary Gel Electrophoresis (CGE)
  • Imaged Capillary Electrophoresis (iCE)
  • Spectroscopic techniques
  • Light obscuration and microflow imaging
  • Additional analytical characterization methods as needed
• Provide general laboratory support, including reagent and consumable ordering, equipment maintenance, continuous improvement activities, and participation in periodic laboratory inspections.
• Collaborate effectively with a multidisciplinary team of scientists to support formulation optimization and overall candidate progression.
• Prepare data summary presentations, support data verification activities, compile and manage datasets, and utilize laboratory data systems such as Empower and electronic laboratory notebooks (ELNs).
• Communicate effectively with laboratory scientists, project managers, and cross-functional colleagues.

Basic Minimum Qualifications:

• At least a BS in Pharmaceutics, Chemistry, Chemical/Biochemical Engineering, Pharmacy, Biochemistry, Bioengineering, Biotechnology, or equivalent 
• 1+ years of industry experience utilizing some sort of chromatography (preferrably HPLC)
• Familiarity with biologics such as proteins, enzymes, monoclonal antibodies, vaccines, mRNA, or antibody drug conjugates and how to characterize them with analytical techniques
• Authorization to work in the United States indefinitely without restriction or sponsorship 

Preferred: 

• Familiarity with HPLC, Capillary electrophoresis, and other analytical techniques
• Strong computer skills and experience with lab-based computer systems
• Ability to collect and analyze data sets

What to Expect in the Hiring Process: 

• 10-15 Minute Phone Interview with Region Recruiter
• 45-60 Minute Virtual Interview with Manager and/or Group Leader
• 30 Minute In-Person Onsite Meeting with the Team

Additional Details: 

The position is  Full Time, Monday-Friday, 8am-5pm.  Candidates currently living within a commutable distance of  Andover, MA  are encouraged to apply.

Excellent full-time benefits include:

• Comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays
• Hourly rate is between $27 -$30, depending on education and experience 

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