Lead Method Validation & Transfer Scientist (Chromatography)

Eurofins BioPharma Product Testing North America; Lancaster (Lancaster County); On-site; USD 90,000 - 125,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA BioPharma Services is seeking a Senior Scientist to validate and transfer analytical methods for APIs and finished products, with emphasis on chromatography and GMP-compliant method validation. The role involves performing validations of methods used for drug product testing and raw materials via HPLC, GC, UV/Vis, and dissolution, and mentoring junior staff.

Ideal candidates will have strong communication, attention to detail, and the ability to work independently or in a team.

Qualifications

• BS/MS/PhD in analytical chemistry or related field required or equivalent.
• 4+ years of industry experience with chromatography.
• 3+ years of LC chromatographic validation in GMP environment.

Responsibilities

• Apply GMP in all areas of responsibility as appropriate.
• Perform validation of analytical methods for drug products and raw materials using HPLC, GC, UV/Vis, and dissolution.
• Read, understand, and interpret diverse analytical procedures.
• Conduct analytical investigations and troubleshoot instrumentation.
• Train and mentor junior staff in laboratory procedures and communicate with clients.
• Manage and discuss projects with clients.

Skills

Communication

Attention to detail

Independence

Teamwork

Adaptability

Self-motivation

Record keeping

Following instructions

Education

BS/MS in analytical chemistry or related

PhD in analytical chemistry or related

Tools

HPLC

GC

UV/Vis

Dissolution

Job description

Eurofins USA BioPharma Services is seeking a Senior Scientist to validate and transfer analytical methods for APIs and finished products, with emphasis on chromatography and GMP-compliant method validation. The role involves performing validations of methods used for drug product testing and raw materials via HPLC, GC, UV/Vis, and dissolution, and mentoring junior staff.

Ideal candidates will have strong communication, attention to detail, and the ability to work independently or in a team.