Sr.Technician for Downstream Manufacturing-Mammalian

<p><b>Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market.</b></p><p></p><p><b>Are you interested in working with the newest equipment and technology and have a background as a process operator in a company working with Äkta Ready, Akta XLSystem and Akta Process? Do you thrive in a dynamic environment with a high pace – this position is for you!</b></p><p>AGC Biologics A/S is a ”Contract Development and Manufacturing Organization” (CDMO) within the biotech industry. We work with developing biopharmaceutical production processes and GMP production of biopharmaceutical proteins for both clinical studies and the market.</p><p><b>About the job</b><br/>You will be a part of our production area, which consist of five production lines that produce preclinical, clinical, and commercial products for a wide variety of different clients across borders. The team consists of dedicated technicians and academics with a high level of professionalism who all work with several partners, e.g. QC, QA, and Development.<br/><br/>As a technician in Downstream, you will be responsible for planning and performing different steps in the production process of protein purification.<br/><br/><b>Your work will include:</b></p><ul><li>Setting up equipment (SUM systems, columns, filters, Äkta Ready systems, ROSS Filling)</li><li>Execution of the processes; HETP, Chromatography, and Filtration (Nano &amp; UF/DF filtration) and final Fill by ROSS.</li><li>Preparing the buffer solutions for production.</li><li>Swabbing and Sampling</li><li>Documentation, Review of MPRs and Logbooks</li></ul><p>Your responsibilities will also include preparing the production room and systems before and after production and participate in qualification, maintenance, control and calibration of the equipment.<br/><br/>Together with the team, you will be responsible for delivering the product to the filling team and ensure high quality in the batch documentation in close collaboration with QA/QC.<br/><br/><b>About you</b><br/>We imagine that you:</p><ul><li>You have a Master of Science degree</li><li>Have +2 year of experience from the biopharmaceutical industry and have worked in a cGMP environment</li><li>Have experience with protein purification with help from chromatography using Äkta Ready or Process</li><li>Interested in equipment maintenance and instruments</li><li>Is good at collaborating and communicating in a constructive manner</li><li>Are able to talk, read and understand English</li></ul><p>As a person, you are positive and flexible and thrive in taking on new assignments and responsibility. You thrive in a dynamic work environment and can handle unpredictability.<br/><br/>Our production team has changing work shifts and you have to be prepared alternately working day, evening, night, weekends, and take on overtime during peak periods.<br/><br/>For further information about this position please contact Hiring Manager Shyam Chelika + 45 22 69 94 64.<br/><br/>We review applications on an ongoing basis, so send in your application today.</p><p><b>Join an international and agile organization</b><br/>At AGC, you will get great opportunities to work with a wide array of tasks and challenges, and you will get experience with our various departments. Furthermore, as we plan projects and tasks together in the team, you will get the opportunity to influence your daily work. AGC offers an informal working environment where high energy and enthusiasm is part of the daily work life. We respect each other and our individual differences. At AGC, we have a flexible attitude and we help each other reach deadlines as a team.</p><p></p><p><b>Want to keep posted about our growth and to learn more about our company?</b></p><p>We also urge you to follow us on our LinkedIn Company Page and give us a quick Like on Facebook !</p><p></p><p>AGC Biologics (AGC) is a global Contract Development Manufacturing Organization (CDMO) with bio-manufacturing facilities in Europe, Japan, Italy and the USA. The company provides a comprehensive range of commercial and clinical cGMP biologics manufacturing services, from DNA to active pharmaceutical ingredient (API). The company’s team and approach are tailored to each of its client’s needs, whether turnkey manufacturing or sophisticated, stand-alone analytical, formulation and stability services.</p><p></p><p>Visit <a href="https://www.agcbio.com/" rel="noopener noreferrer" target="_blank">www.agcbio.com</a> to learn why AGC Biologics is a World Leader in process development and contract manufacturing.</p><p></p><p></p><p><b>Our culture at AGC Biologics is defined by the six core values: Knowledge, Trust, Quality, Ingenuity, Accountability and Teamwork. Our core values stem from our team members and are embedded