Interested in contributing to improving and saving lives?  Eurofins Food Chemistry Madison is growing and we're looking for amazing team members to join us.

In 2021 we moved into a brand new ISO 17025 accredited laboratory in Madison, WI designed to conduct food chemistry testing specializing in infant formula, sole-source nutrition products, hemp and CBD, dietary supplements, and a variety of botanicals. Our testing portfolio includes vitamins, minerals, contaminants, pesticides and shelf-life studies.

We test of a variety of instrumentation including UPLC, HPLC, GC, and LCMS technologies. We offer an innovative and collaborative team environment, and the opportunity to develop expertise on a wide variety of analytical instruments! If you are looking for an opportunity to work for an exciting growth oriented company, we look forward to talking with you!

Assigned Responsibilities/Requirements:

• Perform method feasibility, method validation, and dose analysis on pharmaceutical products (including both hot (radioactive) and cold studies).
• Perform method verification for compendia monographs using a wide array of instrumentation.
• Draft reports using generated results.
• Performs SPV (data review) of data generated by other analysts in the team.
• Work independently on assigned projects and report progress and issues with study direction team and supervisor/manager.
• Draft quality records such as quality events and investigations.
• Understanding of laboratory waste streams and documentation of such activities, which is especially critical for maintaining safe radioactivity levels within laboratory.
• High attention to detail.
• Flexibility in schedule when working on studies based on formulation delivery. Note dates that clinical activities occur is typically scheduled well in advance.
• HPLC experience is desired.

Additional responsibilities depending on prior experience:

• Drafting methods from client provided documents.
• Client facing opportunities in regards to analytical method development.
• Perform instrument qualification activities as needed.
• Draft and modify SOPs for instrumentation and GMP processes as needed.
• Draft quality records such as change controls.
• Perform formulation development testing as needed.

Compensation for this role: $24-$26/hour

To perform this job successfully, the individual must be able to perform each essential duty satisfactorily.  The requirements below are representative of the knowledge, skill or ability required

• 2+  years of relevant experience
• Bachelor’s Degree in relevant field (Laboratory experience may be substituted for degree)
• Familiar with the use of standard laboratory equipment
• Experience with use and troubleshooting of analytical equipment is desired
• Basic knowledge of computers and software programs

Education/Experience (BMQ):

• Bachelor’s Degree in relevant field (Laboratory experience may be substituted for degree)

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

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