Eurofins Viracor, Inc.
Senior Scientist, Biologics Raw Materials
Eurofins Viracor, Inc., Columbia, Missouri, United States,
Senior Scientist, Biologics Raw Materials
Full-timeEurofins 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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.Job Summary:
Eurofins BPT-Columbia is looking for a
Senior Scientist
to join our Biologics Raw Materials team located in Columbia, Missouri. This individual will be a subject matter expert in testing Raw Materials used in Cell and Gene Therapy applications. The successful candidate will perform method establishment and validations under cGMP guidelines on a diverse set of methods including HPLC, GC, Amino Acid Analysis, Mass Spectroscopy and FTIR. Ability to analyze data and effectively communicate results. Ability to complete work in an agreed upon timeline. Train team upon completion of method establishment and validation.Responsibilities include (but are not limited to):Designing, carrying out, and performing 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).Perform method establishment and validations on a diverse set of methods including HPLC, GC, Amino Acid Analysis, Mass Spectroscopy, and FTIR.Analyze data with software including Empower and effectively communicate results.Train and mentor junior staff.Utilize laboratory information management system (LIMS) with proficiency.Adheres to schedule according to Eurofins or contracting organization’s timetable and establishes daily or weekly routines necessary to ensure on-time delivery.Minimum Qualifications:Bachelor’s degree in chemistry, biochemistry, or biology and 5 years of experience working in a cGMP laboratory OR Master’s degree and 3 years of experience working in a cGMP laboratory OR PhD and 1+ years of experience working in a cGMP laboratoryIndustrial experience with method establishment and cGMP validations are highly desirableAuthorization to work in the U.S. without restriction or sponsorshipThe Ideal Candidate Would Possess:Previous experience working in a CRO/CDMO adhering to cGMP regulationsAbility to conduct work efficiently, analyze data to ensure accuracy and report quality data.Good problem solving, time management, communication, and interpersonal skills.The position is full-time, Monday-Friday, 8am-4:30pm, with overtime as needed. Candidates within a commutable distance of Columbia, MO are encouraged to apply.Excellent full time benefits including comprehensive medical coverage, dental, and vision optionsEurofins is an M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
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Full-timeEurofins 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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.Job Summary:
Eurofins BPT-Columbia is looking for a
Senior Scientist
to join our Biologics Raw Materials team located in Columbia, Missouri. This individual will be a subject matter expert in testing Raw Materials used in Cell and Gene Therapy applications. The successful candidate will perform method establishment and validations under cGMP guidelines on a diverse set of methods including HPLC, GC, Amino Acid Analysis, Mass Spectroscopy and FTIR. Ability to analyze data and effectively communicate results. Ability to complete work in an agreed upon timeline. Train team upon completion of method establishment and validation.Responsibilities include (but are not limited to):Designing, carrying out, and performing 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).Perform method establishment and validations on a diverse set of methods including HPLC, GC, Amino Acid Analysis, Mass Spectroscopy, and FTIR.Analyze data with software including Empower and effectively communicate results.Train and mentor junior staff.Utilize laboratory information management system (LIMS) with proficiency.Adheres to schedule according to Eurofins or contracting organization’s timetable and establishes daily or weekly routines necessary to ensure on-time delivery.Minimum Qualifications:Bachelor’s degree in chemistry, biochemistry, or biology and 5 years of experience working in a cGMP laboratory OR Master’s degree and 3 years of experience working in a cGMP laboratory OR PhD and 1+ years of experience working in a cGMP laboratoryIndustrial experience with method establishment and cGMP validations are highly desirableAuthorization to work in the U.S. without restriction or sponsorshipThe Ideal Candidate Would Possess:Previous experience working in a CRO/CDMO adhering to cGMP regulationsAbility to conduct work efficiently, analyze data to ensure accuracy and report quality data.Good problem solving, time management, communication, and interpersonal skills.The position is full-time, Monday-Friday, 8am-4:30pm, with overtime as needed. Candidates within a commutable distance of Columbia, MO are encouraged to apply.Excellent full time benefits including comprehensive medical coverage, dental, and vision optionsEurofins is an M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
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