Exception Writer- Stability & Batch Release Chemist
About the role
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 Organization 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 Organizations. It also has a rapidly developing presence in highly specialized 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 decentralized 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. In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years. Candidates currently living within a commutable distance of Columbia, MO are encouraged to apply.
Responsibilities
- Completing work for research and development under CGMP and/or GLP guidelines for studies, documentation, etc.
- Assisting in conducting, monitoring, and reporting studies to ensure data accuracy and report quality.
- Providing somewhat complex analytical work on projects and studies using a range of analytical techniques and instruments.
- Working with increasing independence on studies and assignments.
Qualifications
- Experience with GLP and/or GMP and hands-on experience with HPLC and/or GC desirable.
- Experience with LIMS system desirable.
- Familiarity and/or experience in a laboratory setting is required.
- Good organizational skills; ability to follow direction and good communication skills are required.
- Ability to work on multiple on-going projects.
- 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.
- 1-3 years of experience working in a cGMP compliant lab.
- Authorization to work in the US indefinitely without restriction or sponsorship.
Benefits
- Comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
Schedule
Full-time position, Monday - Friday 8:00am - 4:30pm.