As a Eurofins Lancaster Labs employee, you will become part of a company that has received national recognition as a great place to work.  We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options.

Eurofins Lancaster Laboratories Professional Scientific Services® (PSS) is a global, award-winning insourcing solution that places our people at our clients’ site dedicated to running and managing laboratory services while eliminating headcount, co-employment and project-management worries.

To learn more about Eurofins Lancaster Laboratories, please explore our website www.eurofinsus.com.

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

• This position will be responsible for performing experimental studies within the Biological Development Sciences area and involves drafting technical protocols and reports, stability reports, formulation reports, etc.

• We are looking for individual with scientific background along with understanding of GxP regulations and with excellent scientific writing skills.

• The position may require individual to work in highly collaborative cross-functional team setting as well as independently at times.

• The individual must be flexible in managing priorities and must be able to function in fast paced environment and with accelerated timelines.

• Bachelor's degree in Biology, Chemistry or other related degree concetration, or equivalent directly-related experience

• ​At least 3-5 years of relevant experience required
• Develop LC-MS/MS methods and qualify LC-MS/MS assays to support discovery, non-clinical and clinical studies. 
• Must have experience with a Triple Quad and QTof instruments for Biotherapeutics analysis.
• Must have protein chemistry background to understand sample prep for mass spectrometry – Immunoaffinity capture, Protein digestion, knowledge of protein/peptide handling for LC-MS/MS analysis.
• Assist Senior Staff with the interpretation of data resulting from analyses of bioanalytical samples within a laboratory information management system (Watson LIMS).
• With guidance from Senior Staff, develop and implement new assays or modify existing assays based on in-depth knowledge of laboratory techniques. 
• Assure documentation compliance with internal policies and regulations.
• Prepare and/or review bioanalytical data, bioanalytical reports, validation reports, standard operating procedures, laboratory notebooks and supplemental study information.
• Assist in troubleshooting efforts within the PK Assay development group.
• Provide input on the design and execution of projects or analyses with hands on involvement.
• Review scientific work in project-related fields and areas of expertise.
• Ensure the availability of adequate laboratory materials and qualify new reagents, as needed. Justify the purchase of new materials and equipment.

• Authorization to work in the United States indefinitely without restriction or sponsorship

All your information will be kept confidential according to EEO guidelines.