Scientist Group Leader

Eurofins

Scientist Group Leader developing analytical methods for pharmaceutical ingredients at Eurofins Scientific. Leading analytical development and ensuring compliance with regulatory guidelines.

Posted 7/25/2026full-timeRemote • Massachusetts • 🇺🇸 United StatesSenior💰 $84,000 - $94,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in analytical method development and validation, ensuring compliance with ICH and Health Authority guidelines. Proficient in utilizing various analytical techniques and maintaining instrumentation within the pharmaceutical industry.

Highest-signal resume keywords

Analytical Method DevelopmentMethod Qualification/ValidationHPLC/UPLCGMP ComplianceLeadership Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Analytical ChemistryMethod DevelopmentMethod ValidationStability TestingRelease TestingProcess DevelopmentTechnical Document AuthoringTroubleshooting InstrumentationAnalytical TechniquesActive Pharmaceutical Ingredients

Tools & Technologies

HPLCUPLCGCNMRUVKFFTIRXRPDLC-MSGC-MS

Industry Keywords

Pharmaceutical IndustryGMPFDAICHRegulatory ComplianceQuality AuditsAudit ReadinessDEA

About the role

Key responsibilities & impact

Lead the design, development, and execution of phase-appropriate analytical methods in compliance with ICH and Health Authority guidelines.
Perform release and stability testing on starting materials, intermediates and API for both development and GMP samples.
Author and review technical documents including method qualification/validation/transfer protocols and reports for analytical procedures.
Maintain and troubleshoot analytical instrumentation.
Responsible for contributing to audit readiness and for participating in quality audits with FDA, other Regulatory Agencies, and customers, as needed.
Ensures work in compliance with all state and federal regulations, including but not limited to GMP, DEA, FDA, etc.

Requirements

What you’ll need

BS in Analytical chemistry or equivalent with 5+ years related experience in analytical development (R&D and method qualification/validation) environment within pharmaceutical industry.
MS in Analytical chemistry or equivalent with 3+ years related experience in analytical development (R&D and method qualification/validation) environment within pharmaceutical industry.
PhD in Analytical chemistry or equivalent with related experience in analytical development (R&D and method qualification/validation) environment within pharmaceutical industry.
Experience with common analytical techniques such as: HPLC/UPLC, GC, NMR, UV, KF, FTIR, XRPD, LC-MS, GC-MS and ICP-MS.
Minimum of 5 years’ experience in method development and validation for small molecules Active Pharmaceutical Ingredients (APIs).
Experience with Process Development of APIs.
Previous leadership experience preferred

Benefits

Comp & perks

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