- Carries out somewhat complex routine 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).
- With guidance, may utilize new equipment and/or develop formulas, processes and methods for solution of technical problems.
- Analyzes organic and inorganic compounds to determine chemical and physical properties.
- Adheres to schedule according to ABC's or contracting organization's timetable and establishes daily or weekly routines necessary to ensure on-time delivery.
- Conducts title/skill appropriate procedures with minimal supervision using laboratory equipment, computer resources, and institutional libraires.
- Prepares standards and specifications for processes, facilities, prodicts, and tests.
- May conduct research on manufactured products to develope and improve products.
- May induce changes in composition of substances by introduction of heat, light, energy, and chemical catalysts.
- Performs data analysis, first level, and peer review of data for accuracy and completedness. Prepares data and reports of completed prjects ensuring auditable quality for publication at completion of contracted work by clients.
- May assist in preparation of data and final reports for completed projects or studies.
- Depending on area of assignment, may be asked to perform ELISA testing for protein expression.
- Depending on area of assignmnet, may conduct research into composition, structure, properties, relationships, and reactions of matter.
- Is likely to work on several projects concurrently.
- May assist in training staff on techniques nevessary to perform laboratory assignmnets.
- May assist or serve as study director, principle investigator, or prject leader for GLP or CGMP studies. May assist in planning the conduct of a study.
- Confers with scientist and colleagues regarding reseaerch, and prepares technical papers and reports.
- Performs other related duties as required and directed.
- Bachelor's degree in relevant field such as chemistry, biocjemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field or degree with comparable coursework in the above areas and a minimum of two years of experience in a directly relevant or demonstrated comparable competency and skill attainmnet is required. A Master's degree in a relevant field may be substituded for the bachelor degree and experience.
- Familiarity and/or experience in a laboratory setting is required.
- Ability to read and understand protocols, SOPs, and techical guidelines.
- Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations.
- Ability to define and solve practical problems, present solutions, establish facts, and draw valid conclisions.
- Knowledge of Microsoft Office and Excel is required.
- Regular and reliable attendance is required.
- Must be able to read, write, comprehend, and speak English
- Authorization to work in the United States indefinitely without restriction or sponsorship.
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Associate Scientist - Columbia, United States - Eurofins USA BioPharma Services
Description
Job Description
Job DescriptionCompany DescriptionEurofins 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 believes it is a global leader in food, environmental, pharmaceutical and cosmetics 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, CDMO, advanced material sciences and in the support of clinical studies.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 55,000 staff across a network of more than 1000 independent companies in over 50 countries and operating more than 800 laboratories. 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, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.
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.
Job DescriptionConducts analysis and experimentation on substances in the laboratory with minimal supervision and using prescribed procedures (protocols, standard operating procedures, methods, etc.). Completes work for research and development, CGMP and/or GLP studies, and documents and reports data in a timely manner according to regulatory guidelines.
Job Duties:
Position is full-time, Monday-Friday, 8am - 4:30pm, with overtime as needed. Candidates currently living within a commutable distance of 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 website
We are looking forward to receiving your application including your expected salary and possible start date via our career website.
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.
