Summary

Eurofins BPT- Advantar is looking for a Scientist to join our Routine Testing team located in San Diego, CA. This position is an intermediate-level professional position involved in somewhat complex day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). Responsibilities include completing work under cGMP and/or GLP guidelines for studies, documentation, etc. Assisting in conducting, monitoring and reporting studies to ensure data accuracy and report quality. Providing somewhat complex analytical work on projects and studies using a range of analytical techniques and instruments. Working with increasing independence on studies and assignments.

Job description

Job Description

Eurofins BPT- Advantar is looking for a Scientist to join our Routine Testing team located in San Diego, CA. This position is an intermediate-level professional position involved in somewhat complex day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). Responsibilities include completing work under cGMP and/or GLP guidelines for studies, documentation, etc. Assisting in conducting, monitoring and reporting studies to ensure data accuracy and report quality. Providing somewhat complex analytical work on projects and studies using a range of analytical techniques and instruments. Working with increasing independence on studies and assignments.

The ideal candidate would possess:

Experience in Biochemistry analytical techniques, both chromatographic and electrophoretic in a GMP environment.
Demonstrated technical experience running HPLC/UPLC, LC/MS, CE, icIEF, Karl Fisher, UV/Vis, and/or SoloVPE instruments
Experience with LIMS system desirable.
Experience assisting with peer reviewing data
Comfortability working with multiple software systems and Excel
A highly motivated staff member that is willing to work on a team, and willing to work with others to teach and learn new skills.
Good organizational skills; ability to follow directions and good communication skills are required

Qualifications

Bachelor’s degree in relevant field such as chemistry, biochemistry, biology, chemical engineering, sciences, or other directly related field or degree with comparable coursework in the above areas and a minimum of two years of experience in a directly relevant or demonstrated comparable competency and skill attainment is required. A Master’s degree in a relevant field may be substituted for the bachelor’s degree and experience. Authorization to work in the United States indefinitely without restriction or sponsorship.

Additional Information

Position is full-time, Monday - Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of San Diego, CA are encouraged to apply.

Requirements

Bachelor’s degree in chemistry, biochemistry, biology, chemical engineering, sciences, or other directly related field or degree with comparable coursework
Minimum of two years of experience in a directly relevant or demonstrated comparable competency and skill attainment
Experience in Biochemistry analytical techniques, both chromatographic and electrophoretic in a GMP environment
Demonstrated technical experience running HPLC/UPLC, LC/MS, CE, icIEF, Karl Fisher, UV/Vis, and/or SoloVPE instruments
Experience with LIMS system desirable
Experience assisting with peer reviewing data
Comfortability working with multiple software systems and Excel
Good organizational skills; ability to follow directions and good communication skills
Authorization to work in the United States indefinitely without restriction or sponsorship

Benefits

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