On-site Analytical Scientist II: Pharma Methods & Analysis

Eurofins USA PSS Insourcing Solutions; Harvard (MA); On-site; USD 65,000 - 72,000; Full time

Benefits offered by this job

Medical, dental, vision

Life and disability insurance

401(k) with company match

Paid vacation and holidays

On-site Devens facility

Job summary

The Scientist II at Eurofins USA PSS Insourcing Solutions in Devens, MA develops and implements analytical procedures for APIs using HPLC/UPLC, GC, FTIR and UV-Vis, supporting API development and manufacturing in a cGMP environment. You will document results and assist with method development, validation and transfer, communicating findings clearly.

This full-time, on-site role requires a BS/MS in Analytical Chemistry with 1–2 years of relevant experience and strong teamwork and written

Qualifications

• BS or MS in Analytical Chemistry with relevant experience in pharmaceutical R&D.
• Experience in cGMP environments, method development, qualification and validation.
• Strong written and verbal communication and ability to work in a team.

Responsibilities

• Perform sample analysis, interpret results; document analyses per SOPs.
• Assist with method development, qualification/validation/transfer activities.
• Prepare high-quality written documentation (notebooks, reports, SOPs).
• Troubleshoot analytical instrumentation and report results.
• Communicate research results clearly in writing and orally.
• Apply cGMP, EH&S and regulatory standards in procedures.
• Support safety and sustainability initiatives.

Skills

Analytical chemistry

HPLC/UPLC

GC

FTIR

UV-Vis

cGMP

Documentation

Teamwork

Education

Bachelor's degree in Analytical Chemistry

Master's degree in Analytical Chemistry

Tools

MS Project

NMR

ICP-MS

FTIR Instrument

Job description

The Scientist II at Eurofins USA PSS Insourcing Solutions in Devens, MA develops and implements analytical procedures for APIs using HPLC/UPLC, GC, FTIR and UV-Vis, supporting API development and manufacturing in a cGMP environment. You will document results and assist with method development, validation and transfer, communicating findings clearly.

This full-time, on-site role requires a BS/MS in Analytical Chemistry with 1–2 years of relevant experience and strong teamwork and written