Manager is open to Post Grad candidates that has technical writing experience from school.
Rhode Island (ARI). Primary responsibilities of this position include support the investigation process, perform investigation, project manager the owning deviations, CAPA generations, lead functional team, communicate with management when situation is holding the progress of the deviations. Skills: ; knowledge of process and faculty equipment, and the ability to interpret and apply Good Manufacturing Practices (GMP); quality assurance or manufacturing experience in the pharmaceutical industry; written and spoken fluency required in specific language needed
Supplement additional workload on team
2-3 years of Technical Writing
Project management knowledge
Call meetings, lead functional team, technical write deviations, work cross functionally with multiple teams (PD, Mfg, QA, QC, SC, Warehouse).
* Candidate will have the opportunity to work in a challenging yet rewarding environment. * This can be assigned special projects related to operational excellent
* From investigation stand point, this candidate will learn the operational process in the biotech operations (QC, Engineering, Warehouse)
No experience in Pharmaceutical industry.
No experience with technical writing
Initial phone interview followed by an in person, and (potentially) panel forum.
management, writing, manager, assurance, Bulk, call, CAPA, Communicate, deviation, drug