Associate Data Review Scientist

Eurofins

Lancaster (Lancaster County)

On-site

USD 55,000 - 75,000

Full time

14 days+

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Benefits offered by this job

Medical coverage

Dental and vision insurance

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins Biopharmaceuticals is looking for an Associate Scientist to support Data Review for the Biochemistry team. This entry-level role offers hands-on development in lab activities and data tracking under prescribed SOPs and CGMP guidelines.

The position balances laboratory work with data tracking duties, ideal for candidates seeking growth in both areas within a GMP environment. Full-time schedule, with potential overtime, located in Lancaster, PA.

Qualifications

Bachelor's Degree in a LIFE SCIENCE field required (e.g., Chemistry, Biochemistry, Biology).
Authorization to work in the United States indefinitely without restriction or sponsorship.

Responsibilities

Review laboratory data for accuracy, clarity, and GMP/GLP adherence.
Review data across multiple areas per SOPs; ensure regulatory requirements are met.
Perform data tracking and reporting with attention to GLP/GMP guidelines.

Skills

Attention to detail

Communication

Teamwork

Independent work

Education

Bachelor's degree in Life Sciences

Tools

Excel

LIMS

Job description

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 Organisation 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 Organisations. It also has a rapidly developing presence in highly specialised 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 decentralised 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

Eurofins Biopharmaceutical is looking for an Associate Scientist to support Data Review of our Biochemistry team. The Associate Scientist position is considered an entry-level opportunity that will allow for hands on development and growth in day-to-day activities supporting a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). The Data Review requirement of this position will also allow for development and assignment of responsibilities that include reviewing scientific reports under CGMP guidelines, assisting with internal audits, review of scientific reports to ensure regulatory requirements have been met, data tracking and reporting.

This position will provide a balance schedule to support both laboratory and data tracking operations and is seeking a potential candidate that is interested in learning both aspects within a lab setting.

Employee Responsibilities And Qualifications

Ensure that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations.
Review simple and complex routine and non-routine data (for three or more areas) according to departmental, corporate, and client SOPs; read and understand analytical procedures; ensure all work is performed according to GLP/GMP requirements and apply GLP/GMP in all areas of responsibility
Experience in a laboratory setting or GMP pharmaceutical setting.
Ensure that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations
Review simple and complex routine and non-routine data (for three or more areas) according to departmental, corporate, and client SOPs; read and understand analytical procedures; ensure all work is performed according to GLP/GMP requirements and apply GLP/GMP in all areas of responsibility as appropriate
Good organizational skills; ability to follow direction and good communication skills are required.
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.

Qualifications

Minimum Qualifications

Bachelors Degree in a LIFE SCIENCE field such as Chemistry, Biochemistry, and Biology required
Authorization to work in the United States indefinitely without restriction or sponsorship

Additional Information

Position is Full-time, Monday-Friday, 8:00 a.m.-5:00 p.m., with overtime as needed. Candidates currently living within a commutable distance of Lancaster, Pennsylvania are encouraged to apply.

Excellent Full-time Benefits Including