Analytical Chemistry Senior Scientist

Company Description

Eurofins Scientific is an international life sciences company which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment and pharmaceutical 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, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the key emerging players in specialty clinical diagnostic testing in Europe and the USA.

Group's key figures are approx. 5.4 billion Euros turnover, over 900 laboratories across 50 countries and about 55,000 staff.

Job Description

If you’re seeking to become engaged in purposeful work that will have a far-reaching impact, Eurofins Agroscience Services (EAS) provides the environment you’re looking for. With more than 50 years’ experience in the crop protection industry, EAS offers a unique portfolio of expertise, providing extensive laboratory and field support across multiple industries including agrochemical, biopesticide, pharmaceutical, biocide, and fine chemical manufacturers.

When you join the EAS Group, you’ll become part a network of laboratories that prioritizes the execution of top-tier scientific studies. With access to specialized equipment and best-in-class instrumentation, you will collaborate with a team of highly trained scientists and study directors to rapidly build upon your existing skills set.

Eurofins Agroscience Services is searching for an Analytical Chemistry Senior Scientist to work in Easton, MD.

Senior Scientist responsibilities include, but are not limited to, the following:

• Develop analytical methods to quantitate analyte(s) of interests in complex sample matrices.  Sample matrices may include complicated aqueous solutions or solid matrices (e.g. sediment or animal diet) containing matrix interferences, naturally occurring background, high salt content, high fat content, etc.
• Design and perform sample processing procedures that may involve extraction, SPE, LLE, clean-up, concentration, solvent exchange, dilution, etc.
• Perform GPL analytical method validations according to EPA, EC, EU, OECD or FDA guidelines.
• Operate, maintain and trouble-shoot analytical instruments (e.g. HPLC, GC, LCMS, GPC, ICP).
• Serve as Study Director for analytical method development and validation used in regulatory toxicity tests.
• Review study information, analytical data, scientific documentation and study reports.
• Serve as an expert in analytical chemistry to support staff and external customers.
• Communicate with staff or external customers on technical issues, project timelines and study related issues supporting eco-toxicity testing.
• Responsible for the quality and accuracy of the data and reports sent to clients under assigned responsibility.
• Manage multiple projects concurrently and work with laboratory management and other staff to ensure project deadlines are met.
• Conduct training of staff on analytical techniques necessary to perform laboratory assignments.

Qualifications

The ideal candidate would possess:

• Demonstrated skills in analytical method development for quantitation of small or large molecules in complex matrices.
• Extensive experience in sample preparation techniques such as LLE, SPE, isolation, separation or purification.
• 3+ years of experience in working with LCMS (Triple quadruple or QTRAP).
• 3+ years of experience in working with HPLC and GC instruments.
• Ability to independently perform data analysis using relevant instrument software.
• Experience in trouble-shooting of analytical methods and investigation of anomalous analytical results.
• Excellent communication (oral and written) skills with people who have different science background.
• 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.
• Familiarity with Microsoft Office Suite and computer skills.
• Ability to work extended hours beyond normal work schedules including weekends and holidays as necessary when assigned.

Basic Minimum Qualifications:

• Bachelor’s degree in relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other related field or degree with comparable coursework in the above areas and a minimum of eight years of experience in a GLP laboratory. 
• A Master’s degree in a