Biopharmaceutical Chemist

Eurofins USA PSS Insourcing Solutions; Groton (CT); On-site; USD 28,000 - 40,000; Full time

Benefits offered by this job

Excellent full-time benefits (medical,

Job summary

Eurofins USA PSS Insourcing Solutions is seeking an analytical chemist to support projects across the clinical drug development pipeline. You will execute test method protocols including solubility, dissolution, precipitation, and flux assays, and prepare analytical solutions for in-vitro experiments.

The role requires experience with HPLC/UV-Vis and data analysis; strong communication is essential for cross-functional collaboration in a fast-paced environment.

Qualifications

• Bachelor's degree in Chemistry, Pharmaceutics, Physical Chemistry, Biochemistry, or a related discipline with 2+ years of relevant experience.
• Master's degree in Chemistry, Pharmaceutics, Physical Chemistry, Biochemistry, or a related discipline with relevant experience.

Responsibilities

• Provide analytical chemistry support to projects across the clinical drug development pipeline.
• Execute test method protocols for in-vitro biopharmaceutics team that includes but not limited to thermodynamic solubility measurement, USP dissolution, precipitation and flux assays.
• Prepare analytical solutions and biorelevant media for in-vitro experiments, including accurate weighing, potency corrections, buffer preparation, and appropriate handling of active pharmaceutical ingredients.
• Analyze study samples by HPLC and UV-vis, including calibration standard preparation, sample processing, and quantitation of drug concentration from in-vitro studies.
• Perform first-pass review of dissolution, solubility, and analytical data, identifying anomalous results (e.g., carryover, precipitation, coning, filtration loss) for scientific follow-up
• Document findings in electronic lab notebooks and technical reports in accordance with ALCOA data integrity principles
• Support routine laboratory operations, including equipment readiness, consumables, safe lab practices, and scheduling instruments
• Adapt experimental execution and prioritization to shifting project needs, balancing scientific rigor with resource efficiency and study objectives

Skills

HPLC

UV-Vis

Data analysis

Communication

Education

Bachelor's degree in Chemistry

Master's degree in Chemistry

Tools

GraphPad Prism

Origin/Origin Pro

JMP

Job description

Job Description

Employee Responsibilities

• Provide analytical chemistry support to projects across the clinical drug development pipeline
• Execute test method protocols for in-vitro biopharmaceutics team that includes but not limited to thermodynamic solubility measurement, USP dissolution, precipitation and flux assays
• Prepare analytical solutions and biorelevant media for in-vitro experiments, including accurate weighing, potency corrections, buffer preparation, and appropriate handling of active pharmaceutical ingredients
• Analyze study samples by HPLC and UV-vis, including calibration standard preparation, sample processing, and quantitation of drug concentration from in-vitro studies
• Perform first-pass review of dissolution, solubility, and analytical data, identifying anomalous results (e.g., carryover, precipitation, coning, filtration loss) for scientific follow-up
• Document findings in electronic lab notebooks and technical reports in accordance with ALCOA data integrity principles
• Support routine laboratory operations, including equipment readiness, consumables, safe lab practices, and scheduling instruments
• Adapt experimental execution and prioritization to shifting project needs, balancing scientific rigor with resource efficiency and study objectives

Qualifications

The Ideal Candidate would possess

• Working knowledge of HPLC and UV-vis spectroscopy techniques, as they apply to quantitation of organic small molecules in solution
• Basic proficiency in scientific data analysis like spreadsheet-based calculations and chromatography data interfaces
• Excellent oral and written communication, strong attention to detail, and strong quantitative ability
• Ability to communicate and collaborate well in a cross functional environment
• Customer focused and comfortable supporting multiple project teams with shifting timelines, with a problem-solving mindset and a positive, optimistic attitude

Preferred Qualifications include

• Hands-on experience executing in-vitro biopharmaceutics testing, such as USP dissolution, solubility, precipitation, or flux assays
• Proficiency in data analytic software like GraphPad Prism, Origin/Origin Pro, JMP etc.
• One to two years of wet lab experience in a pharmaceutical company or at a contracting organization.

Minimum Qualifications

Bachelor's degree in Chemistry, Pharmaceutics, Physical Chemistry, Biochemistry, or a related discipline with 2+ years of relevant experience.

Master's degree in Chemistry, Pharmaceutics, Physical Chemistry, Biochemistry, or a related discipline with relevant experience.

Additional Information

• Position is Monday- Friday 8:00 AM- 5:00PM. Overtime as needed.
• 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
• 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.

Compensation

$25-$25