Contract: 12 monthsRate: €21–€27 per hour (no additional benefits)Location: Waterford siteMust have: FTIR, Scanning electron microscopy, RAMAN spectroscopy.The role provides a strong opportunity to gain experience in sterile manufacturing and to work closely with the MSAT team. For the right candidate, it could serve as a good entry point into Sanofi, with plenty of scope for longer-term opportunities if Waterford is a location that works for you.You would also be engaged as a contractor through a third-party company (e.g. Contracting Plus).· Excellent documentation skills GDP· Effective interaction with other departments on matters related to raw materials, intermediates and finished batch releases. Close contact maintained with Quality Assurance Production, Engineering and Planners.· Maintain, update and issue chemical methods, specifications and SOP's in compliance to pharmacopoeia and regulatory requirements.· Assist with training of the analysts in areas of expertise and knowledge and in new methods, SOP's and updates.· Trend such results, record on COA's where required and complete OOS's investigations on a timely basis.· Update the QC Team Leader on potential problems and highlight improvements where possible by use of the normal communication means.· Ensure all quality documentation and records are complete and current· Ensure QC laboratories meet current Good Laboratory Practice (cGLP) requirements.· Ensure relevant procedures are correctly defined and followed· Ensure that critical chemical testing and related equipment meets current validation requirements (IQ, OQ, PQ) where required.· Audit and review chemistry test results daily and ensure compliance with cGLP.· Checking/auditing laboratory notebooks and analytical reports· Always ensure compliance to cGMPJob Type: Full-timePay: €21.00-€27.00 per hourApplication question(s):FTIR, Scanning electron microscopy, RAMAN spectroscopy. Must haveExperience:pharmaceutical: 1 year (required)Work Location: In person