Sohail Mahmood

Experience

• 

  Forward Gear (Pvt.) Ltd.

  Jul 2016 - Aug 2016

  Former Engineering intern

  During my tenure as an Engineering intern in the maintenance department, I delved into:• Pre-literature knowledge and firsthand experience in maintaining and managing various machineries• Learning valuable insights into practical engineering applications, that enhanced my skill set and understanding of industrial operations.

• 

  Millat Tractors Limited

  Jul 2017 - Aug 2017

  Former Engineering intern

  As an engineering intern at Millat Tractors within the automotive industry, I honed my knowledge in:• Machining processes, IC engines and auto parts assembly• getting hands-on experience to enrich my understanding of automotive intricacies, fostering invaluable growth

• 

  Dr. Frigz International

  Dec 2018 - Jun 2019

  Production Engineer

  I had the following responsibilities as a production engineer:• Ensure all medical devices follow set quality standards and engineering drawings.• Inventory management• Production planning• Product realization• Supply Chain management

• 

  Descon

  Jul 2019 - Aug 2019

  Mechanical Engineering Intern

  As an engineering intern at Descon Engineering Limited in the Oil and Gas department, I focused on:• Comprehending the theoretical aspects behind the component design, including pressure vessels, distillation columns, and foundations• Research work on P.F.D.s, P&IDs, the general arrangement of components, inspection techniques, and engineering drawings• Designing a primary vertical variable diameter pressure vessel, showcasing my understanding and application of learned principles as part of my final assignment Show less

• 

  Goldstar Medical Instruments

  Jul 2020 - Oct 2023

  Quality Assurance Engineer

  As a quality assurance engineer I had following responsibilities:• Process validation to improve MD development and ensure highest standards of quality• Development, review and revise validation master plan (VMP)• Write test protocols, performing testing, and generate comprehensive reports• Implementation of ISO 9001, ISO 13485, and FDA cGMP 21 CFR 820• Validation and revalidation of Ethylene Oxide sterilization process according to ISO 11135• Sterile barrier compliance according to ISO 11607• Biological evaluation of medical devices according to ISO 10993• Monitoring of cleanroom and associated ancillaries according to ISO 14644• Liaise with R&D department to implement ISO 14971• Liaise with R&D department to develop new products and implement design change• Liaise with R&D and regulatory affair departments for technical documentation• Ensuring effective management of the entire lifecycle of software and hardware components utilized in medicaldevice development by using Siemens Polarion ALM along, M-files and CETEC ERP• Process, product and fixture design• Machinery maintenance• Corrective and preventive actions (CAPAs)• Non-conformance handling• Customer complaints handling• Internal and external auditing for compliance Show less

• 

  Getinge

  Jul 2024 - now

  Working Student in Quality Management

  Supporting the Quality Management department in:• Regulatory Compliance in ISO 13485, FDA 21 CFR 820• CAPA Handling• Regulatory affairs