Specialist Data Reviewer, Chemistry - Raw Materials (Chromatography)
Company Description
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.
Job Description
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
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
Additional Information
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.