of the job:
and experienced Regulatory Affairs Scientist (Development and Technical Support) for the Regulatory Affairs
The development of research protocols and the management and organization of data (user studies) User and Clinical Studies: 60%. Conducting user and usability engineering studies, RETSPL studies, and clinical clinical validation studies. Managing all aspects of the research study. Develop research strategies to understand Planning, conducting, and writing up of claims studies. Documentation: 25%. Assisting the Legal & relevant. M. Communication Pathology in Audiology (or studying towards) 2 years of industry experience. R350
The development of research protocols and the management and organization of data (user studies) User and Clinical Studies: 60%. Conducting user and usability engineering studies, RETSPL studies, and clinical clinical validation studies. Managing all aspects of the research study. Develop research strategies to understand Planning, conducting, and writing up of claims studies. Documentation: 25%. Assisting the Legal & relevant. M. Communication Pathology in Audiology (or studying towards) 2 years of industry experience. R350
vacancy for a Head of Medical Affairs. Job Purpose: Develop and maintain in depth knowledge for assigned product(s) relevant congresses, and seminars and by regular self-study of the national/international literature. Provide scientific/technical information; contribute to the development and medical and scientific accuracy of core dossiers standards of best practice. KOLs Management and development Develop & maintain professional and credible the products and areas of therapeutic interest. Develop & maintain scientific expertise of company
medicine and cosmetic manufacturing facility. Develop protocols for executing equipment and facility cleaning validations and temperature mapping studies. Execute protocols, including coordination of activities processes. Maintain accurate tracking of validation studies, equipment and facility status. Review all new good calibration/metrology-based evaluations. Develop, write and update departmental SOPs. Provide subject investigations, change control submissions, new product development and during regulatory and customer inspections
Scientist: Conduct environmental assessments and impact studies to evaluate the effects of projects and activities into strategic initiatives and project planning. Develop and recommend sustainable practices to mitigate conducting environmental assessments and impact studies. Strong analytically skills, with experience using
Scientist: Conduct environmental assessments and impact studies to evaluate the effects of projects and activities into strategic initiatives and project planning. Develop and recommend sustainable practices to mitigate conducting environmental assessments and impact studies. Strong analytically skills, with experience using
activities Plan, coordinate and drive test method development and validation activities Lead and coordinate the execution of hold time study protocols and temperature cycling studies for new products/reformulated costs for reformulation, trial batches, method development, method validation, stability, process validation
activities Plan, coordinate and drive test method development and validation activities Lead and coordinate the execution of hold time study protocols and temperature cycling studies for new products/reformulated costs for reformulation, trial batches, method development, method validation, stability, process validation