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 DescriptionPosition 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 appropriateDemonstrate and promote the company visionRegular attendance and punctualityRead and understand analytical proceduresReview documentation, generated data, calculated results, and final reports according to departmental, corporate, and client SOPsGain a technical understanding of the techniques in which review is being performedUse MS Windows applications such as EXCEL, Word, Access, Outlook emailConducts all activities in a safe and efficient mannerPerforms other duties as assignedQualificationsEducation/Experience (BMQ):
Master’s degree in a science-related field with 1-3 years of experience in Pharmaceutical Chemistry drug product/substance testing with knowledge of regulatory requirements.
Theoretical / Practical experience with analytical techniques such as pH meter, Spectroscopy (UV, IR,), KF, XRD, Particle size testing, Osmolarity. Knowledge of USP/EP compendia, and laboratory software applications such as Waters Empower software, LIMS, Electronic Notebook is preferred.