Analytical Chemist- Method Development & Validation

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

Job Summary

Eurofins Small Molecule Method Establishment is seeking a Senior Scientist to perform method validations, method transfers, and method verification activities on APIs and finished products. The team is seeking candidates with expertise in Chromatography and method validation.

Responsibilities

• Apply GMP in all areas of responsibility, as appropriate.
• Perform a large variety of analytical tasks for the validation of analytical methods used in the testing of drug products and raw materials by means of various procedures including HPLC, GC, UV/Vis, and dissolution.
• Read, understand, and interpret diverse analytical procedures.
• Conduct analytical investigations.
• Troubleshoot instrumentation and communicate with vendors when required.
• Train and mentor junior staff in laboratory procedures.
• Manage and discuss projects with clients.

Qualifications

Minimum Qualifications

• BS or MS degree in analytical chemistry or other related degree concentration.
• BS and 4+ years of industry experience, MS and 2+ years of industry experience, or PhD and 1+ year of industry experience.
• 3+ years of industry experience with chromatography.
• 3+ years of experience with LC chromatographic validation in a GMP environment.
• Authorization to work in the U.S. indefinitely without restriction or sponsorship.

The Ideal Candidate

• Excellent communication (oral and written) and attention to detail.
• Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude.
• Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.

Additional Information

Working schedule will be Full-Time, First Shift, Mon-Fri, 8am-4pm. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. 25% travel may be required. This position is NOT remote.

What we Offer

• 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.

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.