Company Description

Eurofins Scientific is an international life sciences company that provides a wide range of analytical testing services to clients across multiple industries. From food and pharmaceuticals to environmental and cosmetic products, Eurofins ensures safety, authenticity, and accuracy. With a global presence and over 900 laboratories, Eurofins is a leader in food, environmental, pharmaceutical and cosmetic product testing, as well as in genomics, clinical studies support, and other specialized diagnostic testing.

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:  

Exercise discretion and independent judgment with respect to matters of significance directly related to the management or general business operations through the data review process Perform review of scientific data, including, but not limited to standard preparation, calibrations, methodology, QC, sample data, compound evaluation and other subjective review based on testing performed; perform complex calculations to verify resultsVerify the data is of sound quality and determine if data is compliant and defendable based on industry regulations and methodologyMay serve as technical advisor for analysts with regard to QA/QC of dataDiagnose problems; solve simple problems, and suggest solution to complete problems in professional areaKeep oneself and peers abreast of current developments and trends in professional area by reading and understanding internal procedures, attending/providing training sessions, by writing/revising SOPs (as required), and by assisting Group Leader / Principal Specialists in training new and existing employeesUse MS Windows applications such as Excel, Word, Access, Outlook email; create complex Excel worksheets and formulasCommunicate with internal clients to discuss any findings and notify them of any necessary rework or compliance/regulatory concernsConducts all activities in a safe and efficient mannerAttention to detailsWorks in collaborationPerforms other duties as assignedApplies GMP/GLP in all areas of responsibility, as appropriateDemonstrate and promote the company visionRegular attendance and punctualityRead and understand analytical procedures
 

Qualifications

Education/Experience (BMQ:
Master’s degree in a science-related field with 6-10 years of experience in Bio/Pharmaceutical Chemistry drug product/substance testing with knowledge of regulatory requirements. 

Theoretical / Practical experience with analytical techniques such as Ligand binding assays, ELISA, Gel electrophoresis, Proteomics, Flow Cytometry, TEM, PCR, cell culture and cell-based assays (such as reporter gene, cell signaling, and cell proliferation). etc. Knowledge of USP/EP compendia, and laboratory software applications such as LIMS, Electronic Notebook is preferred.

Additional Information

Key Candidate Attributes:

Self-motivation; excellent quality of work and attention to detailAbility to communicate effectively with coworkers and internal/external clientsAbility to learn new tasks quickly and to move easily from task to taskAbility to handle prioritization and multiple tasks simultaneouslyAbility to use a personal computer and learn necessary programsGood communication skills (oral and written)Organizational ability and good judgementScience background/education and/or laboratory experienceStrong Math SkillsLogical Thinking, Good Reasoning AbilityMotivation to excelCoaching/mentoring of peers