What are the responsibilities and job description for the Data Package Specialist position at Eurofins USA BioPharma Services?
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.
Job Description
This 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.
Qualifications
The Ideal Candidate would possess
- Possess, 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 equivalent
- Minimum of 2 years of administrative experience in a fast-paced environment
- Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information
Positions are full-time, working Monday-Friday 8am-5pm, overtime as needed. Candidates currently living within commutable distance to 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 M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
