Specialist Data Reviewer, Chemistry Raw Materials (Chromatography)

ENGLISH

Eurofins Scientific is an international life sciences company, which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the leading global emerging players in specialty clinical diagnostic testing.

In 2018, Eurofins generated 4.2 billion Euro proforma turnover in 800 laboratories across 47 countries, employing about 45.000 staff.

Position Summary:

Ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations

• Essential Duties and Responsibilities:  
  
  •    Applies GMP/GLP in all areas of responsibility, as appropriate
  
  •    Demonstrate and promote the company vision
  
  •    Regular attendance and punctuality
  
  •    Read and understand analytical procedures
  
  •    Review documentation, generated data, calculated results, and final reports according to departmental, corporate, and client SOPs
  
  •    Gain a technical understanding of the techniques in which review is being performed
  
  •    Use MS Windows applications such as EXCEL, Word, Access, Outlook email
  
  •    Conducts all activities in a safe and efficient manner 
  
  •    Performs other duties as assigned

Qualifications

To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements below are representative of the knowledge, skill or ability required. 

Education/Experience:

A master’s degree in Pharmaceutical/Analytical Chemistry

Experience level :

3–5 years of Analytical testing of Pharmaceutical Raw Material (e.g. Chromatographic assay experience mandatory, ROI, LOD, pH, KF, etc) and GMP experience preferred.