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Data Package Associate Specialist
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Eurofins
Lancaster, PA (In Person)
Full-Time
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Job Description
Company DescriptionEurofins 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 Organization 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 Organizations. The Group also has a rapidly developing presence in highly specialized 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 decentralized 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.
Job DescriptionThis position with the Data Package Department is responsible for generating a compiled set of pharmaceutical analytical results to be delivered to our clients. This department receives data in various forms from our laboratories. The data is then assembled into an organized final report within our databases, checked for accuracy, and released as reported analytical results. These results are used by our clients to make important decisions about the quality and safety of pharmaceuticals and medical devices.
QualificationsThe Ideal Candidate would possessPossess, or able to learn, a basic understanding of GMP regulations and expectations.
Comfortable with computer use on a routine basis.
Familiarity with Word, Excel, Outlook, and in-house databases.
Perform administrative duties such as scanning/copying, filing, email, and other office work.
Self-motivated, excellent quality of work and attention to detail.
Ability to work on several tasks simultaneously, under deadlines, and in stressful conditions.
Ability to communicate effectively with coworkers and internal clients.
Ability to learn new tasks quickly and to move easily from task to task.
Communication, organization, good judgement, and versatility in dealing with people
Comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysEurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization 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 Organizations. The Group also has a rapidly developing presence in highly specialized 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 decentralized 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.
Job DescriptionThis position with the Data Package Department is responsible for generating a compiled set of pharmaceutical analytical results to be delivered to our clients. This department receives data in various forms from our laboratories. The data is then assembled into an organized final report within our databases, checked for accuracy, and released as reported analytical results. These results are used by our clients to make important decisions about the quality and safety of pharmaceuticals and medical devices.
QualificationsThe Ideal Candidate would possessPossess, or able to learn, a basic understanding of GMP regulations and expectations.
Comfortable with computer use on a routine basis.
Familiarity with Word, Excel, Outlook, and in-house databases.
Perform administrative duties such as scanning/copying, filing, email, and other office work.
Self-motivated, excellent quality of work and attention to detail.
Ability to work on several tasks simultaneously, under deadlines, and in stressful conditions.
Ability to communicate effectively with coworkers and internal clients.
Ability to learn new tasks quickly and to move easily from task to task.
Communication, organization, good judgement, and versatility in dealing with people
Minimum Qualifications:
High school diploma or equivalentMinimum of 2 years of administrative experience in a fast-paced environmentAuthorization to work in the United States indefinitely without restriction or sponsorshipAdditional InformationPosition is Full-time, Monday-Friday, 8:00 a.m.-5:00 p.m., with additional hours, as needed. 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 optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysEurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.