Analytical Chemist - Proteomics LCMS

Madison, WI, USA Full-time

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years.

Independently executes routine and project assay work for proteomics applications, utilizing primarily LCMS techniques. Participates in method development, optimization, and validation activities for protein or related targets in a variety of complex systems. Assists in method and report document creation with project management and laboratory teams. Analyzes biological or chemical samples for various compounds and components in compliance with appropriate standard operating procedures (SOPs) and regulatory agency guidelines.

A. Duties and Responsibilities:

Indicate positions accountability

_____ GLC/General Manager

_____ Department Head/Function Lead

_____ Manager of Managers

_____ Manager

__X__ Individual Contributor

Essential Duties and Responsibilities:

• Demonstrates and promotes the company vision
• Regular attendance and punctuality
• Applies GMP/GLP in all areas of responsibility, as appropriate
• Organizes, conducts and evaluates analytical results and testing independently in compliance with applicable methods, protocols, SOP’s and regulatory agency guidelines
• Documents work, maintains study documentation and laboratory records.
• Provides input and participates in project meetings
• Executes written method procedures encompassing feasibility, validation, and project work
• Performs peer review and QC review of data
• Performs assigned workload on a daily basis and effectively completes multiple assignments.
• Promotes and contributes to a cohesive team environment and maintains a positive attitude. Plans individual workload in coordination with team members and may plan team workload in coordination with supervisors
• Maintains a clean and safe laboratory work environment
• Understands data generated, and history of methods.
• Recognizes deviations from normal results and inform Study Director, Principal Investigator, and/or management of any problems and/or deviations that may affect the integrity of the data and participates in corrective action of problems.
• Identifies problems and makes suggestions for modifications in test methods or procedures
• Able to adapt to new procedures or particular needs as directed
• Able to identify critical steps in an assay.
• Initiates, drives and implements process improvement initiatives.
• Completes all required training courses.
• Trains, mentors, and assists less experienced staff.
• Assists in evaluation of data for incorporation into written reports.
• Writes reports, methods, protocols and SOPs, and make suggestions for modifications in test methods and procedures.
• Knowledge of departmental procedures and policies
• Effectively plans and utilizes personnel and resources for timely completion of assigned projects.
• Participates in new equipment and instrument assessment and qualification, as appropriate
• Performs complex analyses using unfamiliar or new methods, asking for scientific guidance as needed.
• Conducts all activities in a safe and efficient manner
• Performs other duties as assigned

Basic Minimum Qualifications (BMQ):

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

• Familiar with the use of standard laboratory equipment
• Experience with the use and troubleshooting of analytical equipment is desired
• Ability to perform advanced computer skills (e.g., Word, Excel).
• >1 years’ experience

Education/Experience (BMQ):

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

Additional preferences:

• Experience with HPLC instrumentation is greatly preferred
• Experience with protein analytical techniques is greatly preferred (PAGE, ELISA, LCMS)

Other Factors:

• May work with potentially hazardous substances and/or radio labeled materials
• Mandatory immunizations and screening as required
• May work with potentially hazardous materials.
• Will be exposed to food allergens (ex. Milk, tree nuts, peanuts, fish, shellfish, etc.)
• Work requires some standing and sitting for long periods of time, including working within a laboratory hood and standing at a bench top.
• Work requires use of PPE (personal protective equipment).
• Overtime and weekend work as required
• Will be exposed to potential food allergens.

Principal Contacts and Scope of Communications

¨ Internal: Interacts with internal clients and support groups, operational personnel, scientific personnel and department management

¨ External: Contact with external clients with guidance from scientific or management staff regarding experiment design and outcome. May contact vendors regarding troubleshooting and setup of equipment over the phone or on site

Travel Requirements: ___x___ Yes ______No

¨ <5.0% of the time for potential cross-site support needs or external training.

As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work!

Life at Eurofins is a meritocracy, where people are empowered to make decisions and are rewarded for their success, allowing them to advance quickly. Become your most extraordinary self with support and development throughout your career.

We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, vacation, personal days, and dental and vision options.

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