CPL

PhD Scientist (BB-63EA7)

Found in: Talent IE

Description:
My client is a leading immuno diagnostics company.They have an excellent opportunity available for a Technical Scientist, on a 12 month fixed term contract, with amazing prospects to convert into a permanent colleage. Full benefits are applicable in those once probation is successfully completed.You should have a PhD in a relevant scientific discipline, and possess excellent critical skills thinking.If this sounds of interest, please contact for a confidential discussion.PURPOSE OF THE JOB:To provide the necessary technical support to strategic programmes, ensuring plant meets its customer quality, service, regulatory, financial and safety goals.To provide the necessary technical support to the product manufacturing team, ensuring that production targets are attained.MAJOR RESPONSIBILITIES:Conduct business in a manner that will protect human health, safety and the environment by complying with all applicable EHS laws, as well at the Global and Technical standards.To assist in product development/improvement projectsTo ensure the smooth transfer of new products from other global sitesTo complete and document investigations per site procedures.To design and manage process improvement projects and validations.To work in concert with the manufacturing & quality teams to identify, document, investigate and remedy the cause of product non-conformance in compliance with site CA/PA system requirements.To participate in laboratory maintenance programs, for example instrument maintenance and calibrations, waste disposal and ordering of laboratory reagents.To relate information in the form of presentation to other team members and management.To assist in training team members and technologists as required.To update statistical process control charts and circulate information, highlighting any issues identified.To ensure safety standards are met and safe working practices are adhered to. Suggest where improvements, if any, could be made.To identify and implement cost reductions that do not adversely impact product quality.To bring to the attention of management, areas of risk in the manufacturing, testing and design change process, which might have an adverse effect on product quality and/or safety.To ensure that the plant meets the quality requirements of its customers, internal quality systems, internal & external auditors and other external agencies.To ensure GMP and GLP requirements are maintained.To assist in preparation of the annual departmental budget.To assist in the periodic review of controlled documents per site procedures.EDUCATION & COMPETENCIES:Relevant third level qualification in scientific and/or technical field is desired or relevant combination of education and experienceTwo years experience in the development or support of diagnostic assays or Relevant post-graduate qualification.This experience will ensure awareness and the importance of:following procedures.accurate record problem solving skills.

calendar_today6 days ago

report

info Permanent

location_on Longford, Ireland

work CPL

Apply:
I expressly authorise the Terms and Conditions

Similar jobs