Eurofins Viracor, Inc.
Scientist - Biochemistry Method Development & Validation
Eurofins Viracor, Inc., Columbia, Missouri, United States,
Scientist II - Biochemistry Method Development & Validation
Full-timeEurofins Scientific is an international life sciences company which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment and pharmaceutical products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the key emerging players in specialty clinical diagnostic testing in Europe and the USA.Group's key figures are approx. 6.7 billion Euros turnover, over 940 laboratories across 59countries and about 61,000 staff.Eurofins BPT-Columbiais looking for aScientist tojoin our Biochemistry Method Development and Validation team located in Columbia, Missouri. The Scientist position is an
entry-level
professional position with some industry experience involved in day-to-day activities in a laboratory setting under prescribed procedures (protocols, standard operating procedures, methods, etc.)Perform various tasks and analyses of Bio/pharmaceutical ingredients and products; reviewing or preparing standards and samples for analysis and running a variety of equipment or instrumentation; working efficiently; ensuring that client receives quality data by reviewing laboratory data for accuracy, clarity and adherence to CGMP regulations.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.1-2 years of biopharmaceutical industry experience.The Ideal Candidate Would Possess:Hands-on experience with laboratory analytical instrumentation (HPLC, CE, pH meter, analytical balance, pipettes).Experience in a GMP laboratory setting, preferably experience in handling proteins.Good organizational skills: ability to follow direction and good communication skills are required.Working knowledge of Microsoft Word and ExcelFamiliar with Empower data collection software.Understand and perform calculations as required by test methods.Read and understand analytical procedures (compendial and client supplied) and internal SOP’s.Familiar with ICH Q2 Validation GuidancePosition is a full time Monday-Friday, 8am - 4:30 p.m., with overtime as needed.As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work.Health, Dental, and Vision Insurance401(k) matchingPTO and HolidaysTo learn more about Eurofins, please explore our website www.eurofins.comEurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
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Full-timeEurofins Scientific is an international life sciences company which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment and pharmaceutical products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the key emerging players in specialty clinical diagnostic testing in Europe and the USA.Group's key figures are approx. 6.7 billion Euros turnover, over 940 laboratories across 59countries and about 61,000 staff.Eurofins BPT-Columbiais looking for aScientist tojoin our Biochemistry Method Development and Validation team located in Columbia, Missouri. The Scientist position is an
entry-level
professional position with some industry experience involved in day-to-day activities in a laboratory setting under prescribed procedures (protocols, standard operating procedures, methods, etc.)Perform various tasks and analyses of Bio/pharmaceutical ingredients and products; reviewing or preparing standards and samples for analysis and running a variety of equipment or instrumentation; working efficiently; ensuring that client receives quality data by reviewing laboratory data for accuracy, clarity and adherence to CGMP regulations.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.1-2 years of biopharmaceutical industry experience.The Ideal Candidate Would Possess:Hands-on experience with laboratory analytical instrumentation (HPLC, CE, pH meter, analytical balance, pipettes).Experience in a GMP laboratory setting, preferably experience in handling proteins.Good organizational skills: ability to follow direction and good communication skills are required.Working knowledge of Microsoft Word and ExcelFamiliar with Empower data collection software.Understand and perform calculations as required by test methods.Read and understand analytical procedures (compendial and client supplied) and internal SOP’s.Familiar with ICH Q2 Validation GuidancePosition is a full time Monday-Friday, 8am - 4:30 p.m., with overtime as needed.As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work.Health, Dental, and Vision Insurance401(k) matchingPTO and HolidaysTo learn more about Eurofins, please explore our website www.eurofins.comEurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
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