Scientist I Data Review

Eurofins BioPharma Product Testing North America; Lancaster (Lancaster County); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading company in the life sciences sector seeks a candidate with experience in molecular and cell biology for a full-time position. Responsibilities include ensuring data quality and reviewing documentation. The ideal candidate will have strong communication skills and a background in GMP compliance. Excellent benefits are offered.

Benefits

Comprehensive medical coverage

Dental options

Vision options

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Qualifications

• 1-2 years experience in molecular/cell biology.
• GMP experience required.

Responsibilities

• Ensure high quality data and reports for clients.
• Review laboratory documentation for accuracy.

Skills

Communication

Organizational Skills

Attention to Detail

Education

Bachelor’s degree in molecular/cellular biology

Tools

real-time PCR

ddPCR

ELISA

nucleic acids sequencing

Job description

1 day ago Be among the first 25 applicants

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 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

NOTE: THIS IS NOT A DATA SCIENCE POSITION

Employee Responsibilities

• Ensure that the client receives high quality data and reports that adhere to client and good manufacturing process (GMP) requirements.
• Review laboratory documentation for accuracy, consistency, and clarity.
• Gain a technical understanding of the techniques for the assays in which review is being performed.
• Begin to gain industry knowledge of the testing being completed within the department.
• Document work as required for GMP compliance.

Qualifications

The Ideal Candidate would possess:

• One to two years experience in molecular and/or cell biology, mainly real-time PCR, ddPCR, ELISA, cell based plate reader, and nucleic acids sequencing.
• GMP experience.
• Strong computer, scientific, and organizational skills.
• Excellent communication (oral and written) and attention to detail.
• 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.

Minimum Qualifications

• Bachelor’s degree in molecular/cellular biology or other related degree concentration, or equivalent directly-related experience.
• At least one to two years hands-on experience in a molecular/cell biology laboratory; industry and/or contract testing experience desired.
• Familiarity or experience with GMP setting highly preferred.
• Authorization to work in the United States indefinitely without restriction or sponsorship.

Additional Information

Position is full-time, working 8:00 AM-5:00 PM Monday-Friday. Candidates currently living within a 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 Disabled and Veteran Equal Employment Opportunity employer.