What are the responsibilities and job description for the Scientist, Data Review position at Eurofins BioPharma Product Testing North America?
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 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.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
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.
*THIS IS NOT A DATA SCIENCE POSITION*
Eurofins 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.).
- Review scientific reports under cGMP guidelines to ensure regulatory requirements have been met, the data is whole and accurate, and the report is of high quality.
- Assisting with internal audits
- Work closely with lab operations staff on a day-to-day basis and have the authority and responsibility for final report sign-off.
- Other duties as assigned.
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.
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.
Position is full-time position, Monday - Friday 8:00am - 4:30pm. Candidates currently living within a commutable distance of Columbia, MO are encouraged to apply.
- Excellent full time benefits including comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
To learn more about Eurofins, please explore our website www.eurofinsus.com.
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.