Lead Analytical Scientist - API Methods & Development

Eurofins PSS Insourcing Solutions; Harvard (MA); On-site; USD 84,000 - 94,000; Full time

Benefits offered by this job

Medical, dental, and vision coverage

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA PSS Insourcing Solutions in Devens, MA seeks a Scientist Group Leader to develop and implement analytical procedures for APIs, including potent and peptide projects. Core techniques include HPLC/UPLC, GC, LC-MS, NMR, FTIR, UV-Vis and ICP-MS, with emphasis on ICH compliance and regulatory readiness.

This full-time role offers a pathway to lead method development and validation, contribute to FDA audits, and collaborate with a multidisciplinary team in a dynamic pharmaceutical

Qualifications

• Advanced degree in analytical chemistry with strong development experience.
• Experience with ICH guidelines and GMP/Regulatory expectations.
• Proven ability to develop and validate analytical methods.

Responsibilities

• Lead design and execution of analytical methods for APIs and peptides.
• Perform release and stability testing for development and GMP samples.
• Author/approve method qualification, validation, and transfer protocols.
• Maintain and troubleshoot analytical instruments.
• Support audit readiness and regulatory inspections.
• Ensure compliance with GMP, FDA and related regulations.

Skills

Analytical chemistry

Leadership

Regulatory readiness

Education

BS in Analytical chemistry

MS in Analytical chemistry

PhD in Analytical chemistry

Tools

HPLC/UPLC

GC

NMR

UV

KF

FTIR

XRPD

LC-MS

GC-MS

ICP-MS

Job description

Eurofins USA PSS Insourcing Solutions in Devens, MA seeks a Scientist Group Leader to develop and implement analytical procedures for APIs, including potent and peptide projects. Core techniques include HPLC/UPLC, GC, LC-MS, NMR, FTIR, UV-Vis and ICP-MS, with emphasis on ICH compliance and regulatory readiness.

This full-time role offers a pathway to lead method development and validation, contribute to FDA audits, and collaborate with a multidisciplinary team in a dynamic pharmaceutical