Key Responsibilities

·        Required to monitor, control and manage sutures production area through supervision and proper control.

·        Ensure quality products are produced and production targets (weekly/monthly/annually) are met with required delivery schedules.

·        Ensure all GMP/GDP/ISO13485/FDA regulations and procedures are followed while producing the product.

·        Responsible to support implementing Occupational Health and Safety (OHS) management systems, processes and procedures that improves the Occupational Health and Safety of the employees and other interested parties in according to ISO 45001.

·        Responsible to support implementation of Environment management systems, processes, and procedures in accordance with ISO 14001.

·        Ensure effective control of his/her respective production area in order to achieve production target & required quality standard.

·        Ensure hourly production outputs are achieved by operators as per standard time for the operations.

·        Improve operator productivity and efficiency through continuous monitoring, counseling & training.

·        Implement cell rules in production and monitor same to have orderly production and high-quality standards.

·        Must follow all safety procedures required in sutures department and ensure same are adhered to by his team / subordinates.

·        Ensure that proper production documents are created, recorded and maintained as per GMP/ GDP/ISO13485/FDA requirements.

·        Ensure hygiene and cleanliness is maintained in production areas.

·        Must be able to work in all 3 shifts including night shifts within the company and must be willing to travel abroad and in India for necessary training or for work related activities.

·        Must be able to undertake any other tasks directed by superiors as and when needed.

Travel

·        50+% travel, within country

·        Occasional travel outside country – Trainings & Meetings (as per need)

Key Competencies

·        Good communication & interpersonal skills to interact with various functions in order to coordinate the activities.

·        Strong analytical & problem solving skills

·        High commitment.

Educational Qualification

·        Diploma / B.Tech / Bachelor of Mechanical or Bio Medical Engineering

Experience

·        5 – 8 years of experience of experience in medical device Industry

·        To Handle the Manpower and effective Production Planning

·        Must have Knowledge in ISO 13485, ISO 14001, and ISO 45001

·        Must have good working knowledge in MSOffice.