Senior Analytical Chemist- HPLC Validation

Eurofins BioPharma Product Testing North America; Lancaster (Lancaster County); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Comprehensive medical coverage

Dental and vision options

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

A leading BioPharma testing company is seeking a Senior Analytical Chemist to conduct method validations and perform various analytical tasks. This full-time role requires a BS/MS in analytical chemistry and several years of relevant industry experience, particularly in chromatographic validation. Excellent benefits including medical coverage and 401(k) matching are offered.

Qualifications

• 4+ years of industry experience for BS, 2+ years for MS, or 1+ year for PhD.
• 3-5 years of experience with LC chromatographic validation in a GMP environment.
• Authorization to work in the U.S. without sponsorship.

Responsibilities

• Applies GMP in all areas of responsibility.
• Perform analytical tasks for validation of methods.
• Conduct analytical investigations and troubleshoot instrumentation.
• Train and mentor junior staff.

Skills

Excellent communication

Attention to detail

Self-motivation

Adaptability

Positive attitude

Education

BS or MS degree in analytical chemistry or related field

Tools

HPLC

GC

UV/Vis

Chromatographic validation

Job description

Senior Analytical Chemist - HPLC Validation

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 seeks candidates with expertise in method development and/or method validation.

Responsibilities

• Applies 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

The Ideal Candidate would possess:

• 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.

Minimum Qualifications:

• BS or MS degree in analytical chemistry or related field.
• BS with 4+ years of industry experience, MS with 2+ years of industry experience, or PhD with 1+ years of industry experience.
• 3-5 years of experience with LC chromatographic validation in a GMP environment.
• Authorization to work in the U.S. without immediate or future sponsorship.

Additional Information

Position is full-time, Monday – Friday, 8:00am – 4:00pm. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply.

• 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.

Other

Seniority level: Mid-Senior level

Employment type: Full-time

Job function: Science