Lab Analyst Raw Materials

Contenuto del lavoro

Company Description

Eurofins is Testing for Life. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing, and in discovery pharmacology, forensics, advanced material sciences and agro-science Contract Research services. Eurofins is also a market leader in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in Biopharma Contract Development and Manufacturing. The Group also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. With 58,000 staff across a network of 900 laboratories in 54 countries, Eurofins’ companies offer a portfolio of over 200,000 analytical methods. Eurofins Shares are listed on Euronext Paris Stock Exchange.

Eurofins Professional Scientific Services (PSS) is a global, award-winning insourcing solution. A Eurofins PSS employs and manages full-time analysts, technicians, scientists and technical support personnel directly at the client facility to provide long term staffing needs while maintaining the same services, expertise and cGMP compliance available at the Eurofins facility. Eurofins PSS offers excellent career opportunities for people who have a proven track recording in combining excellent technical ability with first class interpersonal and communication skills.

Job Description

As Lab Analyst, you will be responsible for a long-term program at our client site, a pharmaceutical company leading clinical nutrition solutions formulated to help patients maintain or regain their health. During your mission you will be brought to participate in the feasibility and verification of pharmacopeia methods on raw materials (Titration, Visual testing, UV, Karl Fisher, HPLC, …). You will then implement these methods at the release laboratory.

Responsibilities

• Perform laboratory testing in a qualified environment following procedures (equipment and analytical procedures) and local or global processes, with respect to timeline and planning assigned by team lead
• Conduct the feasibility study of the pharmacopeia methods.
• Conduct the verification of these methods on the release laboratory
• Review the raw data generated by others lab analysts
• Ensure all reagents, raw materials and equipment are available to run testing design, perform experiments, document activities in an appropriate way and follow-up with responsible person in case of deviation or failed acceptance criteria
• Adhere to the quality system requirements and ensure GMP and GDP standards; also adhere to general and specific environmental, health and safety guidelines
• Facilitate the coordination of the activities between R&D and QC laboratory
• Collaborate with R&D Analytical SME’s, QC Lab Personnel and Analytical Leads to ensure project schedules are met

Qualifications

• Bachelor or Master’s in chemistry (or equivalent by experience) with at least 1 year of professional experience in a pharmaceutical company
• Demonstrated in-depth experience in a qualified laboratory (GMP)
• Good knowledge of method validation/verification/transfer design and associated regulations
• Knowledge of GMPs, FDA, ICH, and compendial guidelines.
• Problem-solving expertise
• Good interpersonal skills, and ability to adapt to diverse environments (R&D and QC environment)
• Capable of analyzing and proposing solution for analytical problems through innovative thought and experience
• Very good level of written and spoken French & good level of written English

Additional Information

• Permanent contract
• Working in a dynamic & fast growing international organization
• Flexible working hours (dayshift, Monday-Friday)
• A job with responsibility and variation
• A competitive salary package
• Training & Personal Development opportunities