* Contract: 12 months
* Rate: €21–€27 per hour (no additional benefits)
* Location: Waterford site
* Must 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 cGMP
Job Type: Full-time
Pay: €21.00-€27.00 per hour
Application question(s):
* FTIR, Scanning electron microscopy, RAMAN spectroscopy. Must have
Experience:
* pharmaceutical: 1 year (required)
Work Location: In person