Beschreibung
Project/Freelance - Denmark - Medical Devices - 5 MonthsLadies and Gentlemen,
we are urgently looking for your expertise to consult a global medical devices company in Denmark within the following freelance (!) roles.
Roles:
QC - Manager 1
Experience from a QA position; Exp. With ISO 13485, FDA 21 part 820 regulation, IHC and GMP guidelines; Exp. with Validation of test methods or exp. with standard compendium test methods (pharmacopeia and recognized standards); Exp. from analytical laboratory, preferably Quality Control lab.
QA Validation - Manager 2
Exp. from QA position; Exp. with ISO 13485, FDA 21 Part 820 regulation, GMP guidelines; Exp. with Proccess validation documentation (PFMEA; URS; VMP; IQ; OQ; PQ; monitoring); exp. from production environment, if possible (processes such as purification, mixing, dialysis, filtration, concentration, cleaning)
QC Cleaning validation - Manager 3
Exp from QA position; Exp with ISO 13485, FDA 21 part 820 regulation, IHC and GMP guidelines; exp with cleaning validation documentation (designing test setup, reviewing protocols, approving reports); exp from production environment, if possible cleaning of processes such as purification, mixing, dialysis, filtration, consentration cleaning.
Qualifications: Engineer, Pharmasist or Chemist, please sent your latest CV in English and provide your availability for a engagement in Denmark as well as your expected hourly rates. English at business level is a must, Danish, Finish or similar scandinavian language beneficial.
Please contact us: Real Staffing Group, Freelance Division, Frankfurt/Germany