Biopharmaceutical Chemist

LabRulez

Groton, Northern (CT, KY)

Hybrid

USD 75,000 - 110,000

Full time

40 hours ago
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Benefits offered by this job

Medical, dental, and vision insurance
Life and disability insurance
401(k) with company match
Paid vacation and holidays
Authorization to work in the United St

Job summary

Eurofins Scientific is seeking a Biopharmaceutical Chemist to provide analytical chemistry support across the clinical drug development pipeline. The role involves executing test method protocols for in-vitro biopharmaceutics and preparing analytical solutions and biorelevant media for in-vitro experiments.

Candidate should have hands-on HPLC/UV–vis experience, strong data analysis skills, and the ability to work across cross-functional teams in a fast-paced environment.

Qualifications

  • Bachelor's or Master's degree in Chemistry, Pharmaceutics, Physical Chemistry, Biochemistry, or a related discipline.
  • 2+ years of relevant wet-lab experience in a pharmaceutical setting.
  • Hands-on experience with HPLC and UV–vis for quantitation.
  • Strong data analysis and interpretation skills.

Responsibilities

  • Provide analytical chemistry support across the clinical drug development pipeline.
  • Execute test method protocols for in-vitro biopharmaceutics projects.
  • Prepare analytical solutions and biorelevant media; weigh, buffer, and handle APIs.
  • Analyze samples by HPLC and UV-vis; perform calibration and quantitation.
  • Review dissolution, solubility, and analytical data for anomalies.
  • Document findings in electronic lab notebooks and reports per ALCOA.
  • Support routine lab operations and instrument readiness.
  • Adapt experiments to shifting project needs while maintaining rigor.

Skills

HPLC
UV-vis spectroscopy
Data analysis
Communication
Cross-functional collaboration
Customer focus

Education

Bachelor's degree in Chemistry
Master's degree in Chemistry

Tools

GraphPad Prism
Origin/Origin Pro
JMP

Job 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 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.

In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 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 2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.

Biopharmaceutical Chemist
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 ofGroton, CTare 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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