Scientist I, Data Review at Eurofins

Columbia, Missouri, United States -

Full Time

Start Date

Immediate

Expiry Date

05 Jul, 26

Salary

0.0

Posted On

07 Apr, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Data review, CGMP, GLP, HPLC, GC, LIMS, Empower, Analytical techniques, Laboratory documentation, Quality control, Communication skills, Organizational skills, Attention to detail, Computer skills, Scientific reporting

Industry

Medical and Diagnostic Laboratories

Description

Company 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 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. Job Description Responsibilities include reviewing work for research and development under CGMP and/or GLP guidelines for studies, documentation, etc. Assisting in reviewing, monitoring and reporting studies to ensure data accuracy and report quality. Providing somewhat complex analytical review work on projects and studies using a knowledge of analytical techniques and instruments. Working with increasing independence on studies and assignments. The ideal candidate would possess: Experience with GLP and/or GMP and knowledge of HPLC and/or GC. Experience with LIMS system desirable. Experience reviewing Empower. Familiarity and/or experience in a laboratory setting is required. 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 and a minimum of 6 months of experience in a directly relevant or demonstrated comparable competency and skill attainment is required. A Master’s degree in a relevant field may be substituted for the bachelor’s degree and experience. Authorization to work in the United States indefinitely without restriction or sponsorship. Additional Information Position is a full time Monday-Friday, 8 a.m.-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. To learn more about Eurofins, please explore our website www.eurofins.com Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Responsibilities

The Scientist I is responsible for reviewing research and development data under CGMP and GLP guidelines to ensure accuracy and quality. They will perform complex analytical reviews and assist in monitoring and reporting studies while working with increasing independence.