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
- Focus on assay implementation and maintenance, including reagent and instrument qualification, as well as assay troubleshooting in support of Gene therapy and Protein modalities
- Work with a team supporting Biopharmaceutical Process Development for products in all stages of development
- Perform biological activity assays in multiple formats, quantitative assays to measure viral titer, genome titer, and assays measuring the levels of residual host DNA, protein, and other process-related impurities
- Data analysis using various software packages
- Preparation of technical reports and standard operation procedures
Qualifications
- BS + 10 years experience, MS + 5 years experience, or PhD in Virology, Molecular Biology or related Biological Sciences
- Previous work with AAV- or lentivirus-based Gene therapy products and automation experience preferred
- Previous experience with cell-based bioassays in 96-well format, qPCR/ddPCR, and sandwich immunoassays with various readouts (fluorescence, electrochemiluminescence, ELISA) is required
- Expeirence withcell culture and cell banking
- Accurate record keeping
- Excellent laboratory, computer, documentation and organizational skills
- Good communication abilities
- Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information
Position is full-time, Monday - Friday 8:00am - 5:00pm.Candidates currently living within a commutable distance of Cambridge, MAare 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
Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
Company:Eurofins USALocation:Cambridge - Massachusetts - United StatesJob Types:Full TimePost Date:November 1, 2021Valid Through:November 30, 2021