– Manage the quality system and work with regulatory bodies and the production line.
– Coordinate work in accordance with internal and external specifications and standards.
– Write, review, and approve company documents, specifications, and procedures.
– Improve processes, participate in internal audits, and carry out corrective and preventive actions.
– Manage change control activities and monitor design development activities.
– Coordinate work in accordance with internal and external specifications and standards.
– Write, review, and approve company documents, specifications, and procedures.
– Improve processes, participate in internal audits, and carry out corrective and preventive actions.
– Manage change control activities and monitor design development activities.
Requirements:
– Bachelor’s degree (BSc) or higher in life sciences, biology, chemistry, biotechnology, or related fields – required.
– Must possess extensive knowledge of quality requirements.
– Experience and understanding of regulatory requirements in the Medical Device field.
– At least 5 years of experience in the medical device industry.
– Fluent in English.
– Bachelor’s degree (BSc) or higher in life sciences, biology, chemistry, biotechnology, or related fields – required.
– Must possess extensive knowledge of quality requirements.
– Experience and understanding of regulatory requirements in the Medical Device field.
– At least 5 years of experience in the medical device industry.
– Fluent in English.
This position is open to all candidates.
