About this role
<p> </p> <p><img style="width:970.0px;height:400.0px" src="https://performancemanager5.successfactors.eu/doc/custom/wackerchem/Jobs_Header_English_blue_970x400_1.jpg"></p> <p> </p> <p><span style="font-size:14.0px"><span style="font-family:Arial, Helvetica, sans-serif">Do you want to take responsibility and make a difference with your work? With your expertise, we can achieve great goals together. We are WACKER - Reliable. Determined. Ambitious. As one of the world's most research-intensive chemical companies, we've been making countless products that are an integral part of your everyday life possible for over 100 years. From vegan food to resource-efficient buildings to solar cells, we develop sustainable solutions that change the future.</span></span></p> <p> </p> <p><span style="font-size:14.0px"><span style="font-family:Arial, Helvetica, sans-serif">Wacker Biotech, as part of WACKER, is a leading global biotechnology organization specializing in the production of biopharmaceuticals. The company has outstanding technologies for the rapid, efficient and thus cost-effective production of therapeutic proteins for clinical and commercial supply. Currently it is the biggest dedicated microbial Contract Development & Manufacturing Organization (CDMO) in the world. lts four dedicated and fast-growing production sites are currently based in Germany (Halle and Jena), The Netherlands (Amsterdam) and The United States (San Diego, CA). At our Amsterdam-based center Wacker Biotech B.V. focuses on the GMPcompliant microbial based production of recombinant proteins, vaccines and live microbials as drug substance and drug product.</span></span></p> <p> </p> <p style="text-align:center"><span style="font-size:14.0px"><span style="font-family:Arial, Helvetica, sans-serif">To strengthen our team in <strong>Amsterdam,</strong><br>we are looking for you as a(n) <strong><strong>MSAT - Process Engineer</strong></strong></span></span></p> <p> </p><p><strong>Job requirements</strong></p> <p>• Ensuring technology transfer from and to production by being the production representative in the relevant project core-team(s) by ensuring that the execution of the production (associated) work within the company is scientifically and technologically correct, efficient, and cost-competitive (within the boundaries of SHE and cGMP requirements, as well as client´s expectations); <br>• Ensuring life-cycle management of a process from transfer, via process validation to continuous process verification; <br>• Ensuring, if needed, process related support to shop-floor for production activities.</p> <p> </p> <p><strong>Qualifications Required</strong></p> <p>• Academic or HLO level - bioprocess field of expertise;<br>• Working for 5 years or more in a (Bio-) pharmaceutical environment or in a relevant (bioprocess) research field;<br>• Extensive knowledge of (bio)pharmaceutical processes with experience in downstream processing, specifically protein / polysaccharide purification;<br>• Document writing skills in English;<br>• At ease in project teams, interacting with clients, training colleagues, working in matrix structures;<br>• Application knowledge of GMP standards (writing batch documentation and SOPs);<br>• Familiar with process validation, trending, data analysis;<br>• Capability to coordinate and perform technology transfer and process validation activities within the manufacturing organization;<br>• Capability to prepare accurate documentation (batch documentation, validation documentation, scientific reports);<br>• Capability to resolve problems;<br>• Capability to summarize and present complex information in an audience-appropriate format (operators, clients, management etc.);<br>• You reside in and are eligible to work in The Netherlands (valid work permit).</p><p> </p> <p><span style="font-size:14.0px"><span style="font-family:Arial, Helvetica, sans-serif"><strong>What do we offer?</strong></span></span></p> <p> </p> <ul> <li><span style="font-size:14.0px"><span style="font-family:Arial, Helvetica, sans-serif"><strong>Employment:</strong> A challenging and international position in a professional and informal working environment</span></span></li> <li><span style="font-size:14.0px"><span style="font-family:Arial, Helvetica, sans-serif"><strong>Compensation: </strong>Attractive salary, holiday allowance, home-office travel allowance, participation in the company's success, subsidized pension plan</span></span></li> <li><span style="font-size:14.0px"><span style="font-family:Arial, Helvetica, sans-serif"><strong>Work-life balance:</strong> Flexible working hours (where possible), 30 days of vacation</span></span></li> <li><span style="font-size:14.0px"><span style="font-family:Arial, Helvetica, sans-serif"><strong>Versatile development opportunities:</strong> Support for professional development</span></span></li> </ul> <p><span style="font-size:14.0px"><span style="font-family:Arial, Helvetica, sans-serif">As an international company, we welcome the diversity of people. We consciously promote equal opportunities and a diverse, inclusive culture in our teams - this is what makes us successful.</span></span></p> <p> </p> <p><span style="font-size:14.0px"><span style="font-family:Arial, Helvetica, sans-serif">We look forward to receiving your application!</span></span></p> <p><span style="font-size:14.0px"><span style="font-family:Arial, Helvetica, sans-serif"><strong>Reference Code: <strong><strong><strong><strong><strong><strong><strong>31128</strong></strong></strong></strong></strong></strong></strong> </strong></span></span></p>