required for CE marked devices Responsible for writing Clinical Investigation Plans Provide clinical input and standards (ISO 14155) Experience in medical writing, conducting systematic review and clinical data confidential information Excellent scientific writing / report writing skills Communication skills (written and
required for CE marked devices Responsible for writing Clinical Investigation Plans Provide clinical input and standards (ISO 14155) Experience in medical writing, conducting systematic review and clinical data confidential information Excellent scientific writing / report writing skills Communication skills (written and
experience having worked on planning, running and writing up ISO 17025 validations to submit is essential and research thinking.
experience having worked on planning, running and writing up ISO 17025 validations to submit is essential innovative and research thinking. Must be able to write sops according to minimum standards. Must have strong
experience having worked on planning, running and writing up ISO 17025 validations to submit is essential innovative and research thinking. Must be able to write sops according to minimum standards. Must have strong
reasoning skills with excellent scientific report writing abilities will be required
reasoning skills with excellent scientific report writing abilities will be required
Office suite
hazardous materials or practices Experience in writing reports and policies for health and safety Familiarity
hazardous materials or practices Experience in writing reports and policies for health and safety Familiarity