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Posted 2 days ago by Akira Recruitment
This would include production and maintenance of the DRM, design programme, RFI schedule, MIDP, (in conjunction with the CDE), IRS, statutory condition trackers, design change and risk trackers and design documentation required to achieve practical completion. Taking ownership of design … more
We found 1 job outside your search area.
Posted 23/10/2024 by SEDA Talent
Reverse engineering of commercial reference products. Manage manufacture of products for clinical evaluations and ensure on time delivery of test articles. To drive risk analysis in support of the Tech Transfer process within the Pharmaceutical Department in regard to formulations, … more
