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Analytical Chemist

Eurofins Scientific

Groton, CTFull-timeNo compensation foundPosted 1w agoVerified open 4 days ago
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At a glance

Compensation
No compensation found
Location
Groton, CT
Schedule
Full-time
Work Authorization
Not specified

Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Eurofins Scientific is hiring an Analytical Chemist. The Analytical Chemist is responsible for utilizing analytical methodologies, systems, and processes to support drug substance and drug product development throughout all phases, preparing and analyzing samples using techniques such as HPLC, UPLC, LCMS, GC, spectroscopy, dissolution, and others, while supporting method development, qualification, validation, transfer, stability studies, and ensuring quality, safety, and documentation compliance.

Key focus areas include Utilize analytical methodologies, systems, and processes to support drug substance and drug product development throughout all phases., Prepare, set up, and analyze drug substance product samples using techniques such as HPLC, UPLC, LCMS, and GC., and Support development and optimization of analytical methods, including assay, purity, dissolution, and impurity characterization..

Important skills include HPLC, UPLC, LCMS, GC, GCMS, and SFC.

Skills & qualifications

RequiredNice to have

Skills

HPLCUPLCLCMSGCGCMSSFCUV-VisNMRKFpHROIeLNAnalytical Method DevelopmentMethod QualificationMethod ValidationMethod TransferStability StudiesDegradation StudiesData IntegrityElectronic Laboratory SystemsGMP ComplianceStrong Computer SkillsScientific SkillsOrganizational SkillsExcellent CommunicationAttention to DetailIndependent WorkCollaborationSelf‑MotivationAdaptabilityPositive AttitudeLearning New TechniquesMultitaskingAccurate Record KeepingFollow InstructionsCompliance With Company Policies

Qualifications

Bachelor's Degree in ChemistryBachelor's Degree in BiochemistryRelated Degree Concentration or Equivalent ExperienceExperience in GMP LaboratoryExperience in Analytical ChemistryExperience With eLN and Data TrendingAuthorization to Work in United States Indefinitely Without Sponsorship

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match
Paid Time Off

Full job description

  • Responsible for utilizing analytical methodologies, systems , and processes to support drug substance and drug product development throughout all phases. 

  • Prepare, set up, and analyze drug substances and/or drug product samples using a variety of analytical techniques including chromatography (e.g., HPLC, UPLC, LCMS GC, GCMS, SFC), spectroscopy (e.g., UV-Vis, NMR), dissolution, and other relevant methodologies (e.g., KF, pH, ROI).

  • Support development and optimization of analytical methods, including assay, purity, dissolution, and/or impurity characterization approaches as appropriate.

  • Execute method qualification, validation, and transfer activities to support development and commercialization programs.

  • Conduct degradation, stability, and investigational studies to support the evaluation of product performance and risk.

  • Assess stability, dissolution, and/or impurity trends to support product and process development decisions.

  • Support analytical method and technology transfer activities across laboratories and development sites.

  • Operate, maintain, calibrate, and troubleshoot analytical instrumentation under guidance.

  • Read and understand analytical methods, SOPs, compendial procedures, and GMP requirements while maintaining accurate documentation and data integrity within electronic laboratory systems.

  • Demonstrate strong ownership of quality, safety, productivity, organization, and client service expectations. 

  • Perform other duties as assigned

  • Bachelor’s degree in chemistry, biochemistry, or other related degree concentration, or equivalent directly-related experience  

  • Basic laboratory skills and following written procedures, protocols, and work instructions accurately

  • Strong computer, scientific, and organizational skills

  • Excellent communication (oral and written) and attention to detail

  • Ability to work independently and as part of a team, self-motivated, adaptability, and a positive attitude 

  • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies

  • Experience in GMP laboratory, analytical chemistry 

  • Experience with eLN and data trending

  • Position is full-time, working Monday-Friday 8:00 a.m.-5:00p.m overtime as needed

  • 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

  • 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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