Data Review Specialist

Eurofins•Winston-Salem, NC

1d•Onsite

About The Position

Eurofins Scientific is an international life sciences company providing a unique range of analytical testing services to clients across multiple industries. The company aims to make life and the environment safer, healthier, and more sustainable. Eurofins laboratories work with major companies globally to ensure product safety, ingredient authenticity, and accurate labeling. The Eurofins network is a global leader in food, environment, pharmaceutical, and cosmetic product testing, as well as agroscience Contract Research Organisation services. It also holds a significant market position in specific testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences, and clinical study support, with an expanding presence in Contract Development and Manufacturing Organisations. Additionally, it is rapidly growing in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. Over 30 years, Eurofins has expanded from a single laboratory to a network of 900 laboratories in over 54 countries, employing 58,000 staff. Eurofins companies offer over 200,000 analytical methods to assess the safety, identity, composition, authenticity, origin, traceability, and purity of biological substances and products. In 2021, Eurofins achieved EUR 6.72 billion in revenue and has been a top-performing stock in Europe for two decades.

Requirements

Bachelor’s degree in chemistry, biology, or other related degree concentration, or equivalent directly-related experience (2 years of directly related industry experience is equivalent to 1 full-time year of college in related major).
Minimum of 2 years of experience in laboratory chromatography analyses, Quality, Regulatory, or related experience.
Authorization to work in the United States indefinitely without restriction or sponsorship.

Responsibilities

Reviews simple routine and non-routine laboratory data for one or more areas according to departmental, corporate and client Standard Operating Procedures, Work Instructions, and/or Forms.
Reads and understands analytical procedures.
Ensures all work is performed according to ISO17025 guidelines, GLP Regulatory, and GMP Regulatory requirements.
Performs independent auditing of laboratory data to ensure continuous compliance to both the quality system and regulatory requirements.
Maintains the highest level of proficiency in terms of those duties and responsibilities as required by auditors/data reviewers.
Performs mathematical calculations as part of data review.
Interacts both directly and indirectly with laboratory staff members to ensure all data review are appropriately and efficiently corrected and documented.
Responsible for ensuring the integrity of laboratory data.
Communicates in writing and in person with laboratory personnel and/or with the client in an intelligent and clear manner.
May assist in conducting laboratory investigations, exceptions, planned deviations, and/or corrective and preventative actions.
May assist in training of laboratory personnel.
May assist with Quality and Regulatory Audits and interact directly with auditors.
May assist with Technical Writing and/or Report Writing.