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. Experienced Analytical Scientist with expertise within HPLC AGC Biologics Copenhagen AGC Biologics offers a dynamic working place and an excellent opportunity for working and growing with a varied array of tasks and challenges. You will get insight into and experience with the way the various departments interact throughout a biologics contract development and manufacturing organization in order to achieve success. Exciting and challenging assignments will keep coming your way, and you will to a large extent be able to plan your daily work on your own. AGC Biologics offers an informal working environment, where humor is part of the daily work life. We respect each other and our individual differences. AGC employees have a flexible attitude and we help each other to reach deadlines together as one team, in accordance with our slogan - Right On Time. The Department The AD department is responsible for implementation, transfer and development of analytical methods, and support of Upstream and Downstream Process Development and non-GMP Manufacturing with analytical results. Furthermore, the responsibilities include AD studies e.g. non-GMP stability, in use stability, forced degradation, cleaning verification, interim reference material, characterization analysis, peak characterization etc., working according to GLP supplying GMP-level data and documentation. AGC projects range from early pre-clinical development through all phases of clinical development all the way to commercial supply. AD is also involved in cross functional project groups and implementation of new analytical technologies and techniques. Within this broad working area, with many different customer projects and with various biopharmaceuticals, the AD department differs from traditional AD labs. AD has a close collaboration with customers, and departments across the organization to provide data, demonstrating control of all steps in the manufacturing processes. Role and Responsibilities As a scientist in Analytical Development HPLC, you will be involved in a wide range of exciting tasks and challenges. You will be responsible for implementing and developing new assays within HPLC and electrophoretic methods in close collaboration with external customers and colleagues in AD. Furthermore, you will collaborate with multiple stakeholders including process development, project managers and QC. You will be introduced to a large diversity of biopharmaceutical analytical methods and be an active player in their executions, interpretation of data and reporting. Additional responsibilities: Transfer, development and Implementation of analytical procedure within AD HPLC. Troubleshooting and scientific support on a broad range of bioassay method Representation of Analytical Development (AD) in cross-functional project teams. Verbal and written reporting to clients. Approval and reporting of analytical results to internal and external customers. Transfer of analytical procedures to QC. Coordinating external testing. Qualifications / About you In our new colleague, we are looking for a person with: Higher educational background in Protein Chemistry, Biochemistry , Biochemical or Chemical engineering, or related scientific/technical background(MSc. or PhD) 10 years of experience in an analytical setting preferably with experience within bioassay methods for biologics. Experience, theoretical and hands-on, with bioanalytical methods e.g. SEC, IEX, RP, iCE, CE-SDS. Good English communication skills in writing and speaking, and ability to effectively communicate and interact with team members, colleagues and clients of various cultural backgrounds, with ability to obtain buy-in from all key stakeholders Interested? Please apply online by uploading your application and CV. We are screening for candidates on an ongoing basis, so do not hesitate to enter your submission. If you have further questions, please contact Vanessa Baj, HPLC implementation Manager, Analytical Development, phone 45 2760 3005, or Helle Grann Wendelboe, Senior Director of Analytical Development, phone 45 2294 3090. About AGC Biologics AGC Biologics (AGC) is a global Contract Manufacturing Organization (CMO) with biomanufacturing facilities in Europe, Japan 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. AGC Biologics also offers non-exclusive license to CHEF1™, a proprietary CHO cell line development platform. CHEF1 delivers stable, high-titer, production-quality cell lines in optimized time frames. It is the foundation of CMC Biologics’ innovative approach to cell line and process development. Visit www.agcbio.com to learn why AGC Biologics is a World Leader in process development and contract manufacturing. Andre oplysninger {TravelAmount} 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 into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe. AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com. Want to keep posted about our growth and learn more about our company? Follow us on LinkedIn and give us a quick Like on Facebook! AGC Biologics offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances. AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com.