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Form of workJob Description
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 labeling 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 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.
Eurofins BioPharma Product Testing has delivered expert scientific support to companies working to improve human and animal health. As a member of the Eurofins BPT team, you will work alongside respected technical experts dedicated to scientific excellence in a process driven regulatory compliant environment.
Job DescriptionEurofins BPT-Columbia is looking for a Associate Scientist, Data Review to join our Quality Assurance team located in Columbia, Missouri. The Quality Assurance Associate position is an entry-level position involved in day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.).
Responsibilities include reviewing scientific reports under CGMP guidelines, and assisting with internal audits. The Quality Assurance Associate I review scientific reports to ensure regulatory requirements have been met, data is whole and accurate and the report generated is of high quality. Quality Assurance Associates work closely with laboratory operations staff on a day-to-day basis and have the authority and responsibility for final report sign-off.
Qualifications*not a coding or data science position*
The ideal candidate would possess:
- Experience in a laboratory setting or GMP pharmaceutical setting.
- Good organizational skills; ability to follow direction and good communication skills are required.
- Strong computer, scientific, and organizational skills.
- 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.
- Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
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.
- Authorization to work in the United States indefinitely without restriction or sponsorship.
Additional Information
Position is full-time, Monday-Friday, 8 a.m.-4:30 p.m., 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 with dental and vision options, life and disability insurance, 401(k) with company match, paid holidays and PTO.
To learn more about Eurofins, please explore our website www.eurofinsus.com.
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.
