Commissioning & Qualification Engineer

Job Description

<ul><li>Being responsible for the generation and maintenance of the Commissioning and<br><br></li></ul>Qualification relevant procedures and documents.<br><br><ul><li> Create &amp; execute C&amp;Q protocols and reports under for the relevant Process<br><br></li></ul>Equipment<br><br>Handle and support external/internal validation technicians during planning and<br><br>execution of C&amp;Q activities.<br><br><ul><li> Work with the Engineering team and the Quality Assurance team to define priorities<br><br></li></ul>on the C&amp;Q of new equipment.<br><br><ul><li> Being responsible for the management of Change Controls and Deviations related to<br><br></li></ul>the relevant equipment commissioning and qualification.<br><br><ul><li> Support the Engineering team to improve compliance and quality.</li><li> Supports in troubleshooting and root cause investigation as a technical SME.</li><li> Align with local and global Engineering networks for the corresponding global<br><br></li></ul>activities, to define and implement new technical standards for new technologies and<br><br>equipment.<br><br><ul><li> Collaborate with technical development, other sites, and the global engineering<br><br></li></ul>network to facilitate the transfer of technology.<br><br>Technical Skills, Knowledge and Qualifications:<br><br><ul><li>Engineering background</li><li>2-5 years of experience in pharma industry</li><li>Good technical skills and interest (electrical and mechanical).</li><li>Knowledge of GMP requirements related to system validation.</li><li>Quick learner and good eye for details.</li><li>Fixed contract for 2 years (contingent worker for project purpose)</li></ul>