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.
Completing all training in a timely and complete manner; working with an experienced analyst/mentor performing various tasks and analyses of Bio/pharmaceutical ingredients and products; reviewing or preparing standards and samples for analysis and running any equipment or instrumentation independently and/or with guidance; working efficiently; ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations.
Primary Responsibility: Data review for laboratory data. A background in Biology, Microbiology, etc. is required to be considered for this role.
Applies GMP/GLP in all areas of responsibility, as appropriate
Applies the highest quality standard in all areas of responsibility
Demonstrates and promotes the company vision
Demonstrates strong client service skills, teamwork, and collaboration
Proactively plans and multitasks to maximize productivity
Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration
Regular attendance and punctuality
Performs laboratory operations with good dexterity, good laboratory technique, and high degree of accuracy and precision
Perform/Review preparations of reagents, samples, and standards according to procedures.
Document testing, observations, deviations, and results clearly and completely, and in compliance with regulatory requirements - striving to minimize errors
Understand and perform calculations as required by test methods
Understand and utilize computers for information access, calculations, and report preparation
Read and understand analytical procedures (compendial and client supplied) and internal SOP's
Use MS Windows applications such as Excel, Word, Outlook email
Process data, generate reports, and evaluate data
Communicate effectively, both orally and in writing
Independently seek out work
Perform laboratory maintenance
Commitment to occasional overtime as workload requires
Conducts all activities in a safe and efficient manner
Ensures good housekeeping with a neat, clean and orderly workspace
Performs other duties as assigned
Communicates effectively with client staff members
To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements below are representative of the knowledge, skill or ability required.
Bachelor's degree in scientific concentration
MUST have authorization to work in the US indefinitely without restriction or sponsorship
Experience with chromatography, PCR, laboratory data review
Good dexterity
positive attitude
solution driven
good work habits (organized, efficient, careful, safety-conscious, accurate)
attention to detail
sound scientific logic
good oral and written communication skills
understanding of instrumentation
client service focused
demonstration of organizational skills
ability to work with moderate supervision upon training completion on assigned task
ability to handle multitasking
Position is full time, Wed-Sat 12pm-10pm, training schedule is M-F 8am-4pm. Candidates currently living within a commutable distance of Lancaster, PA are 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 USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
Originally posted by Eurofins. View original posting
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