Associate Scientist - Biotherapeutics at Eurofins in Saint Charles, Missouri

Job 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 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 is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins 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. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.


In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. 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.


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 Description



The Associate Scientist will support the Discovery Services in contract research services to advance new pharmaceutical candidate testing. This position is primarily responsible for routine laboratory assays, mammalian tissue culture, and site equipment support.

• Perform work in a laboratory setting, meeting the physical job requirements of a lab role


• Conduct production assays employing molecular biology and other relevant methods


• Maintain cell culture in a BSL2 laboratory, and adhere to cleanroom guidelines and aseptic technique, according to protocols


• Generate data by performing lab assays in Biotherapeutic Services and other Panlabs units if required


• Contribute to scientific community, and site research and development objectives


• Support internal and external communication regarding handling and shipping of samples for Biotherapeutics


• Receive all deliveries for Biotherapeutics, sort and distribute supplies, as required. Complete associated receiving documentation


• Apply and demonstrate proficiency in electronic notebook and/or record-keeping


• Perform data calculations and analysis using various electronic platforms, e.g. Excel, GraphPad Prism, etc. and provides QC review of data and project reports


• Support the site's equipment management program


• Complete required training and support 100% of Employee Health and Safety requirements


• Demonstrate proficiency with, care and maintenance of department equipment and assets


• Conduct responsible use of confidential IT and business systems, as required


• Adhere to department SOP's and documentation requirements, maintain accurate data management and reporting. Create departmental DQs and SOP's as needed


• Participate in departmental audits to comply with quality standards


• Perform work in a laboratory with physical job requirements of the role


• Prepare and manage inventory of buffers, reagents, media, semi-finished and finished goods


• Support unit goals and demonstrate Eurofins' competencies, as defined in the job plan


• Provide training to colleagues and external end users, when required


• Work effectively in a team environment, under minimum direction, to achieve business key performance metrics of quality and delivery on time


• Adjust work hours and provide cross-functional support to other departments, as required, and maintain accountability in delivering to client needs/timelines


• Routinely communicate project updates to internal and external clients


• Perform other duties, as assigned

• B.A. or B.S. with at least 2 years of relevant experience


• M.A. or M.S. with at least 1 year of relevant experience


• Or an equivalent of education and experience


• Capacity to work independently, with minimal oversight upon completion of training program


• 1 year experience with aseptic technique and mammalian cell culture


• 
  Authorization to work in the US for any employer, indefinitely, without sponsorship
  

• Experience with cell-based assays


• Experience with molecular biology, DNA/RNA extraction a plus


• Experience in a contract research laboratory or clinical setting


• Experience with pipetting controls and standards


• Experience with good documentation practices


• Experience with in vitro laboratory assays

• Good organization and documentation skills


• Good communication and interpersonal skills


• Attention to detail and strong quality control acumen


• Ability to read, write, and interpret documents, such as standard operating procedures and technical reports


• Ability to perform mathematical calculations, statistical analyses, and data interpretation


• Ability to multitask with organization and manage time effectively


• Ability to solve practical problems and troubleshooting skills


• Ability to work in a laboratory setting, according to the physical requirements of a laboratory role


• Lab equipment and office computer/software proficiency


• Demonstrates a positive attitude, capacity for team environment, dedication for quality, and exhibits a genuine interest in drug discovery in support of advancing human health

• 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