Summary

Eurofins BioPharma Product Testing North America is the largest network of harmonized bio/pharmaceutical GMP product testing laboratories worldwide, providing comprehensive laboratory services for pharmaceutical, biopharmaceutical, and medical device companies. As a leading Contract Research Organization (CRO), the company offers extensive testing capabilities for drug substances, final products, intermediates, and starting materials for both small and large molecule drug products. Operating under GMP authorization, ISO 17025 accreditation, and ISO 9000 certification, Eurofins performs analyses according to international pharmacopeial standards including Ph. Eur., BP, USP, and JP. With over 2 million square feet of global laboratory capacity spanning 20 countries and more than 45 locations worldwide, the company maintains seven key US sites in Lancaster, PA; Portage, MI; Columbia, MO; Cary, NC; Charlotte, NC; Jacksonville, FL; and San Diego, CA. Their comprehensive service portfolio includes method development and validation, release testing, stability testing, characterization testing, residuals and impurities testing, extractables and leachables testing, viral clearance studies, and cell and gene therapy testing. The company's harmonized quality procedures, centralized LIMS, and secure 24-hour data access via LabAccess.com provide clients with consistent, reliable testing services that support drug development from early stages through commercialization.

Job description

Job Description

Set-up and conduct in vitro experiments in accordance with protocols and standard operating procedures.
Efficiently carry out procedures necessary to complete each project with minimal supervision.
As appropriate, perform procedures under aseptic conditions.
Actively assist in development and execution of novel testing protocols and overall assay development.
Maintain cell lines.
Prepare test solutions in accordance with directions.
Meticulously maintain precise records in accordance with good laboratory practices.
Assist in writing of reports.
Follow all PSL safety requirements.
Oversees all laboratory assays and day to day procedures.
Creates and maintains lab assay schedule.
Leads training of In Vitro Scientists.
Other duties as assigned.

Qualifications

B.S. degree or equivalent experience in laboratory animal medicine, toxicology, animal science, or biology is preferred.
Must have 2 years of industry experience with cell culture
Prefer someone with hands-on experience in a GLP setting

Requirements

B.S. degree or equivalent experience in laboratory animal medicine, toxicology, animal science, or biology preferred
Must have 2 years of industry experience with cell culture
Hands-on experience in a GLP setting preferred

Benefits

Medical, Dental & Vision
Life & Disability Insurance
401(k) Matching
Paid Vacation & Holidays

Company overview

Eurofins BioPharma Product Testing North America is the largest network of harmonized bio/pharmaceutical GMP product testing laboratories worldwide, providing comprehensive laboratory services for pharmaceutical, biopharmaceutical, and medical device companies. As a leading Contract Research Organization (CRO), the company offers extensive testing capabilities for drug substances, final products, intermediates, and starting materials for both small and large molecule drug products. Operating under GMP authorization, ISO 17025 accreditation, and ISO 9000 certification, Eurofins performs analyses according to international pharmacopeial standards including Ph. Eur., BP, USP, and JP. With over 2 million square feet of global laboratory capacity spanning 20 countries and more than 45 locations worldwide, the company maintains seven key US sites in Lancaster, PA; Portage, MI; Columbia, MO; Cary, NC; Charlotte, NC; Jacksonville, FL; and San Diego, CA. Their comprehensive service portfolio includes method development and validation, release testing, stability testing, characterization testing, residuals and impurities testing, extractables and leachables testing, viral clearance studies, and cell and gene therapy testing. The company's harmonized quality procedures, centralized LIMS, and secure 24-hour data access via LabAccess.com provide clients with consistent, reliable testing services that support drug development from early stages through commercialization.