QC EM Analyst

Company Description

***We have an opportunity for a QC EM Analyst to join our PSS Site in Kinsale****

What can Eurofins offer you as an employee of ours?

• Developmental opportunities and career progression
• The opportunity to work with our client - a world -leading pharmaceutical and biotechnology company
• Location is easily accessible
• Private Medical Insurance 
• Income protection and life assurance
• Annual discretionary bonus
• Free parking onsite
• Full use of the canteen facilities on the client site
• Additional annual leave days with continued service
• The opportunity to work on therapeutic drugs helping to save lives across the world

Consider joining Eurofins, where people are the most important element in our business. Eurofins is a leading contract research organisation providing testing and research services in the pharmaceutical and biopharmaceutical sciences to clients worldwide.

For more information about Eurofins PSS® please visit our website and watch a message from our Global Head, Beth Di Paolo.

This position is to join our innovative Professional Scientific Services (PSS) programme as an employee of Eurofins.  The programme places full-time analysts, technicians, scientists and technical support personnel managed by Eurofins 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. This award-winning programme 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

The purpose of this job is to perform scientific procedures and produce accurate results within the required time frame under the customer quality system, using customer company procedures, and while adhering to Eurofins Lancaster Laboratories general policies and standards.

Job Responsibilities

• Performing routine and non-routine analysis, as requested by the Group Leader or customer representative.
• Preparing and approving results for tests in which they have received the appropriate training and are deemed competent.
• Notify immediately to the Group Leader or a customer representative, any anomalous or out of specification results.
• Participating in all training required and scheduled by the Group Leader or the customer. Being prepared and on time for that training. Engaging in training processes and ensuring all information received is completely understood.
• Completion of training records, and ensuring that all records presented for review and approval are at the appropriate standard.
• Providing training to other team members as instructed by the Group Leader. Ensuring all training delivered is documented appropriately.
• Ensuring at all times that all documentation and laboratory records are up to date and of an appropriate standard.
• Ensuring that all work carried out is approached  “Right First Time” so as to avoid any re-work or errors.
• Gain a clear understanding of all related customer supplemental processes such as deviation handling, training documentation, document and records control.
• Being constantly aware of customer’s requirements and striving to meet or exceed those requirements keeping in mind the customer process end points.
• Gaining a clear understanding of the customer relationship and service goals. Gaining a clear understanding of the customer process flow in terms of destination and use of data generated, and consequences of sub-standard data.
• Dealing with customer queries and to contact designated personnel with any relevant information or issues relating to test results or the service in general.
• Keeping up to date with any technological or method revisions in their area, ensuring their training is complete and adjusting their work as required with approval from the Group Leader.
• Performing second person verification checks as required by the laboratory schedule
• Performing QC samples in accordance with customer procedures.
• Assisting in the processing of laboratory consumables as required – labelling, acceptance testing.
• Revising SOPs and updating other documentation as required by the Group Leader.
• Providing cover for other members of staff as required and for taking part in the customer’s weekend rota and/or overtime schedule.
• Ensuring that all documentation is completed on time.  Ensuring that it is accurate and legible and conforms to the relevant quality standards.