Cognition Specalist

at  Eurofins Ireland PSS

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.
  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 serve as a Documentation Analyst, specializing in Cognition to work to the highest standards in terms of quality and professionalism.

Job Responsibilities

• Stability data reporting for regulatory filings (IND, BLA). Perform date review as required.
• Updates to Shelf-life memos and Annual stability reports.
• Support stability lead in BLA preparation (batch analysis and justification of specifications).
• Work with the Cognition Cockpit global support team to resolve any issues with the system.
• Implement continuous developments and enhancements to the Cognition Cockpit system.
• Keep up to date with existing and new SOP’s and official documentation.
• Perform other duties as designated by Management.
• Independently write/revise SOP’s or other official documentation and reports, when required.
• Execute independently assigned projects.

QUALIFICATIONS

• A Bachelor Degree or Master Qualification in Chemistry, Biology or a related field with knowledge of analytics and/ or stability.
• At least 2-3 years of industry experience
• Mathematical and/or analytical preference
• Practical analytical laboratory experience in a GMP environment is preferred
• A good basic knowledge of some of the following techniques (SEC-HPLC, RP-HPLC, Capillary SDS, Capillary IEF, Residual Moisture pH, Turbidity, UV, Particulate Analysis – sub Visible, MDI ELISA, Bioassays) is an advantage
• Experience with LIMS systems is desirable
• High attention to detail
• Ability to work well within team structures and priced leadership[ and provide leadership is required
• Good communication skills both internally and externally

Additional Information

• This is an opportunity to join Eurofins on a full time permanent basis.
• Benefits of pension contribution, medical insurance, health insurance and bonus are included in package.
• Eurofins Management and Team on client site for support.
• Opportunity to get to know fantastic people and be part of a great team.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, 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 in the support of clinical studies.

• Stability data reporting for regulatory filings (IND, BLA). Perform date review as required.
• Updates to Shelf-life memos and Annual stability reports.
• Support stability lead in BLA preparation (batch analysis and justification of specifications).
• Work with the Cognition Cockpit global support team to resolve any issues with the system.
• Implement continuous developments and enhancements to the Cognition Cockpit system.
• Keep up to date with existing and new SOP’s and official documentation.
• Perform other duties as designated by Management.
• Independently write/revise SOP’s or other official documentation and reports, when required.
• Execute independently assigned projects