Details.
Create high-quality, scientifically accurate documentation for Class I, IIa, IIb and III medical devices under the MDR, including CEP, CER, PMCFP, PMCFR, SSCP and gap analyses. Work to demanding schedules and collaborate effectively with cross-functional groups to ensure consistency between related documents. The page states that applicants should have more than 3 years of experience in the medical field.