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 believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. 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, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

The candidate will support a client group that is responsible for developing robust and efficient purification processes of recombinant proteins and other biological therapeutics from the early to late stages of development.

We are seeking an analytical scientist who will work in a collaborative environment to be engaged in the analysis, monitoring, and characterization of in-process samples to support the group in improving process performance by optimizing product recovery and impurity removal. This role will provide routine analytical testing. Knowledge and expertise in analytical biochemical techniques are a must, ideally including real-time qPCR, ELISA, HPLC, and capillary gel electrophoresis (CGE). The successful candidate must be self-motivated and able to work independently, be accountable for their results and prioritize their workflow, and seek opportunities to take on new projects.

Job Responsibilities and Requirements:

Experience with protein chemistry, protein analytics, and bioprocess technology is requiredExpertise in analytical chemistry using a broad range of separation, chromatographic, spectroscopic, and other detection techniques to characterize and monitor the protein purification processHands-on experience and working knowledge of techniques, including but not limited to RT-qPCR, UPLC/HPLC (size-exclusion, hydrophobic, ion-exchange, affinity), ELISA, and CGEA working knowledge of Empower, control, and data analysis software is strongly preferredWork closely with colleagues by providing quality data to support product development through all clinical phases promptly; uses understanding of analytical tools to assess and interpret experimental dataMaintain written records (electronic lab notebooks and databases) of all experimental work following Good Laboratory PracticesLead in the routine calibration, maintenance, and troubleshooting of laboratory instruments, systems, or apparatus, and may interact with internal site or external vendors in the maintenance and continuous improvement of safe and effective working practices

QualificationsBachelor's or Master's Degree in Biotechnology, Biochemical Engineering, Analytical Chemistry, Chemical Engineering or other related disciplines4-6 years of relevant experienceExperience with RT-qPCR, ELISA, HPLC, and CGEAbility to follow established procedures independently and be accountable for prioritizing own workflow to meet defined metrics and timelinesStrong oral and written communication skillsMust be authorized to work in the U.S. without restriction or sponsorship

Additional Information

What to Expect in the Hiring Process: 

10-15 Minute Phone Interview with Region Recruiter45-60 Minute Virtual Interview with Manager and/or Group Leader30 Minute Virtual Interview with Site Director 

Additional Details: 

The position is full-time, first shift, Monday-Friday, Candidates must be flexible to adapt to schedule changes requiring shift changes and/or weekend work, and overtime may be required as needed. Candidates living within a commutable distance of Rensselaer, New York, are encouraged to apply.  

Excellent full-time benefits include:

comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidayYearly goal-based bonus & eligibility for merit-based increasesPay is between 21 and 23 per hour with a 10% shift differential 

Eurofins Lancaster Laboratories Professional Scientific Services® (PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites, dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.

We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our clients’ quality systems and equipment.

To learn more about Eurofins Lancaster Laboratories, please explore our website www.eurofinsus.com.

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.