Pharmaceutical Development Analytical Scientist

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:

Bachelors degree in Chemistry Pharmaceutics Physical Chemistry Biochemistry or a related discipline with 2 years of relevant experience.

Masters 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.

Remote Work :

No

Employment Type :

Full-time