Principal Scientist, Late Stage Downstream Process Development

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.

Do you want to be part of a company that helps customers bring new advanced biological products to market? Do you thrive in a role where you work closely with customers to improve patients’ lives by advancing biopharmaceuticals to market? If so, this role as a Principal Scientist in our Late-Stage Development team could be the perfect fit for you.

About the Team and Department

Our Late-Stage Process Development Department plays a crucial role in transitioning processes from clinical scale to commercial manufacturing. The department consists of three teams, where you will be part of a group of highly dedicated technicians and scientists collaborating on process characterization and optimization. Our teams drive projects forward through close collaboration across different technical disciplines. You will be part of a dynamic and flexible work environment with many opportunities to contribute and grow.

About the Role

We develop processes for products produced in both mammalian and microbial cell lines and collaborate closely with stakeholders such as Analytical Method Development and Manufacturing.

Your Primary Tasks Will Include…

• Planning, coordinating, and participating in laboratory activities and experiments

• Evaluating results and ensuring data integrity

• Authoring and reviewing protocols and reports

• Providing scientific and technical support

Your Qualifications…

• A relevant Master’s or PhD in biochemistry, protein chemistry, process technology, or a related field, with at least 5+ years of industry experience

• Strong experience in developing downstream process unit operations

• High expertise in late-stage development and process characterization

• Deep understanding of late-stage and commercial production

• Knowledge of regulatory aspects of biopharmaceutical processing

• Strong ability to plan, execute, and report development studies

• Flexibility and a proactive approach to taking on new tasks and responsibilities

• Strong interpersonal and communication skills, both internally and with external customers

• Ability to manage multiple projects simultaneously

• Experience with Design of Experiments (DoE), statistics, and scientific writing is a plus

• Positive mindset inclined to taking on new challenges and thriving in a dynamic environment.

• Strong adaptability and ability to work effectively in situations of uncertainty.

• Fluency in English, both written and verbal

Application

• To apply, please submit your CV. We encourage you to apply even if you do not meet every requirement.

• If we see a potential match, one of our recruiters will contact you to discuss your application.

• If both sides remain positive after this discussion, we will proceed to the assessment stage to evaluate the key skills required for the job.

• For further information regarding the position, please contact the Tove M.I.E. Christensen, Manager in Late Stage Process Development, at +45 2294 3019.

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.