<div class="show-more-less-html__markup show-more-less-html__markup--clamp-after-5 relative overflow-hidden"> <strong>Location:</strong> Germany (Remote – with occasional travel to client in Dresden)<br/><br/><strong>Employment Type:</strong> Full-time / fixterm to 2 year's<br/><br/><strong>Business Unit:</strong> Technology &amp; Engineering<br/><br/><strong>About The Role<br/><br/></strong>We are looking for a Senior Technical Coordinator (m/f/d) to join a high-impact customer project within the pharmaceutical manufacturing domain. In this role, you will act as a key interface between technical teams and the client, ensuring seamless delivery coordination, driving agile practices, and supporting process standardization across manufacturing sites. This is a fully customer-facing position requiring strong communication, technical expertise, and domain knowledge.<br/><br/><strong>Key Responsibilities<br/><br/></strong><ul><li>Lead end-to-end delivery coordination while acting as Scrum Master for the project</li><li>Facilitate issue resolution and drive effective stakeholder communication</li><li>Support change closure processes and ensure timely implementation</li><li>Design and develop custom scripts based on business requirements</li><li>Analyze and understand pharma manufacturing processes</li><li>Identify common processes across multiple manufacturing sites and design Global Process Instructions (PIs)</li><li>Validate Process Instructions (PIs) and enable QA review processes</li><li>Create and maintain documentation related to development, validation, and process standardization</li><li>Engage directly with the client on a daily basis, ensuring alignment and transparency<br/><br/></li></ul><strong>Required Skills &amp; Experience<br/><br/></strong><ul><li>6–8 years of relevant professional experience in a similar role</li><li>Strong hands-on experience with Siemens Opcenter Pharma</li><li>Proven expertise in the scripting module within Siemens Opcenter</li><li>Solid knowledge of VB Script and Oracle SQL</li><li>Strong understanding of pharmaceutical validation processes including IQ, OQ, PQ, and GxP compliance</li><li>Experience in designing Process Instructions (PIs) based on customer requirements</li><li>Ability to identify and standardize processes across manufacturing environments</li><li>Experience in validation of PIs and preparation of supporting documentation<br/><br/></li></ul><strong>What You Must Have To Be Considered<br/><br/></strong><ul><li>Bachelor’s degree or equivalent qualification in a relevant field (engineering or science related degree prefeed but not mandatory)</li><li>Strong analytical and problem-solving skills</li><li>Excellent communication and stakeholder management capabilities</li><li>Ability to work independently in a remote, client-facing environment</li><li>Agile mindset with experience in Scrum methodologies<br/><br/></li></ul><strong>Contact the Recruiter<br/><br/></strong>Sophie Künzel<br/><br/>Email: Sophie.Kuenzel@cognizant.com </div>