Senior Scientist - Biochemistry
Eurofins BioPharma Product Testing Columbia, LLC

Company Description

Eurofins is the world leader in the bio/pharmaceutical testing market. With over €5.3billion in annual revenues and 55,000 employees across 900 sites in50 countries, Eurofins is a leading international group of laboratories providing an unparalleled range of testing and support services to the pharmaceutical, biopharmaceutical, food, environmental, and consumer products industries and to governments.

The Eurofins BioPharma Product Testing (BPT) Group is the largest network of harmonized bio/pharmaceutical GMP product testing laboratories worldwide. Eurofins BPT provides comprehensive CMC laboratory services for the world's largest pharmaceutical and biopharmaceutical companies. The service portfolio supports all stages of the drug development process and all functional areas of bio/pharmaceutical manufacturing, including method development, microbiology, process validation and quality control.

Job Description

Eurofins BPT-Columbiais looking for aSr. Scientistto join our Biochemistryteam located in Columbia, Missouri. The Sr. Scientist is an advanced position, involved in planning own work and supervising day-to-day activities in the laboratory working under prescribed procedures (protocols, standard operating procedures, methods, etc.). Completes complex work for research and development, CGMP and GLP studies and documents and reports data in a timely manner according to regulatory guidelines. Plans the conduct of a study; monitors study procedures to ensure data accuracy and report quality; conducts complex analysis and experimentation on substances, for purposes such as product and process development and application, quantitative and qualitative analysis and improvement of analytical methodologies. Typically serves as technical leader within group and may be the project leader/study director on complicated projects.

Responsibilities include:

• Designs, carries out, and performs simple and complex experiments and procedures in accordance with all applicable regulatory (e.g. DEA, EPA, FDA, FIFRA, OECD, etc.) requirements as defined by protocol, method, and standard operating procedures (SOPs).
• Routinely develops procedures and methods for the solution of technical problems.
• Performs progressively more complex procedures and experiments.
• Is able to utilize equipment, facilities, and personnel to produce sound scientific results in a timely fashion for Eurofins clients.
• Serves as an expert for technical issues for staff and external customers.
• Adheres to schedule according to Eurofins or contracting organization's timetable and establishes daily or weekly routines necessary to ensure on-time delivery.
• Designs and conducts most procedures independently using laboratory equipment, computer resources, and institutional libraries.
• Prepares standards and specifications for processes, facilities, products, and tests.
• Conducts studies to determine and deliver results involving the composition, structure, properties, relationships, and all critical parameters of the material contracted for testing.
• Performs complex data evaluations, reviews the work of others, and writes complex technical reports and standard operating procedures.
• Responsible for the quality and accuracy of the data and reports sent to clients under assigned responsibility.
• Depending on area of assignment, handles regulated materials (quarantined matrices, DEA-controlled and radiolabeled materials, etc.), potential biohazard materials, and toxic chemicals according to company procedures.
• Depending on area of assignment, performs ELISA testing for protein expression.
• Likely to work on several projects concurrently and may monitor and direct activities of other staff performing work in area of expertise.
• Conducts training of staff on techniques necessary to perform laboratory assignments.
• May serve as study director, principal investigator, or project leader for GLP and CGMP studies. May assist in planning the conduct of a study.
• Confers with scientists and colleagues regarding research, and be required to prepare technical papers and reports.
• Performs other related duties as required and directed.

Qualifications

Minimum Qualifications:

• Bachelor's degree in relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field or degree with comparable coursework in the above areas and a minimum of fouryears of experience in a directly relevant setting.
• Master's degree in a relevant field and twoyears of directly relevant experience may be substituted for the bachelor's degree and experience.
• PhD in a relevant fieldmay be substituted for bachelor's degree and experience.
• Authorization to work in the United States indefinitely without restriction or sponsorship.

The ideal candidate would possess:

• Superior knowledge of scientific discipline; basic relevant technical skills; ability to read and understand protocols, SOPs, and technical guidelines.
• Experience with protein characterization, including peptide mapping and intact mass by LC/MS.
• Experience with HPLC, CE, icIEF, Empower software, Analyst software, Unifi software, Protein characterization, Peptide mapping
• Compliance with, and knowledge of, regulatory guidelines and company SOPs (CGMP, GLP) is required.
• Good organizational skills and the ability to follow direction.
• Ability to instruct and provide technical direction to others is required.
• Ability to consult with clients and knowledge of date submission requirements for clients is necessary.
• Excellent communication (oral and written) and attention to detail
• Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
• Knowledge, use, or calibration of a wide range of laboratory equipment

Additional Information

The position is full-time, Monday-Friday, 8am-4:30pm, with overtime as needed. Candidates who live within a commutable distance from Columbia, MO are encouraged to apply.

As a Eurofins 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 PTO, and dental and vision options.

To learn more about Eurofins, please explore our websitewww.eurofinsus.com.

We are looking forward to receiving your application including your expected salary and possible start date via our career website.

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

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