Seeking a well-organized industry that can provide me the opportunities to put my theoretical knowledge into practical work and enhances my practical ideas and technical skills. Prospecting an internship in a corporate environment to enhance my professional familiarity with a range of real-world attitudes, with the ultimate aim of becoming a resourceful individual
Documentation, Record and Implementation as per the ISO 9001:2015, ISO
13485:2016, ISO 14001:2015 and ISO 45001:2018.
Implemented these ISO standards and work on the regulatory compliance in
more than 30 companies
Lean Manufacturing, 6 Sigma, Kaizen for stream line manufacturing
Non Conformity Assessment
Develop policies as per the standard requirements
Internal Auditing as per the standard requirement
Customer Complaints Handling, Investigation and Corrective measure as per
the practice
Training and Effectiveness, Evaluation, and Need Assessment as per the
personnel responsibilities
Resource Management
Management Responsibility
Inspection and Testing as per the specifications and requirements of the
customers
Develop SOPs and WIs as per the processes of the department and
manufacturing procedures
Working related to the Regulatory requirement of the EU MDR 2017/745
Classification, Pre technical files, Applicable EN ISO standard related to the
medical devices
Grip on the ISO, DIN and ASTM standard related to medical devices
Quality Tools (Check sheet, Histogram, Pareto chart, Cause-and-effect
diagram (fishbone diagram), Scatter diagram, Flowchart, and Control chart).
Applying the SPCs (Collecting data, identifying trends and taking corrective
action) developing the processes standards.
Process Validations and HACCP (Hazard , Analysis, Critical, Control and
Points).
Face the External Audits, 2nd Party Audits, and COC Audit
Worked as a research assistant for Heat Treatment and Phase
Transformation Lab related to the students course and lab work.
Monitor and Control daily Inspection.
Prepare daily, weekly & monthly inspection for analysis.
Resolve problems related to quality.
Preparation of SOP, work instructions& process control plan for general running parts.
Monitor and prepared gauges and fixtures calibration reports of parts inspection.
To make sure that execution of quality plans must be according to decided plan.
To update the status of quality plans. To follow up material arrival and delivery for product supply.
Perform in-house cost calculation and improve process efficiency to reduce in-house cost.
To assure completion of supply targets within time and on time delivery to customer.
To evaluate problem solving method in case of any complain from customer.
Supervise routine maintenance and repair works for equipment.