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. Mammalian Production Coordination Team, is part of the Manufacturing Department responsible for preparation of buffer and media for the production of Drug Bulk Intermediate (DBI) / Active Pharmaceutical Ingredient (API) for pre-clinical, clinical and commercial use. The team delivers buffer and media for four of our five production lines working 24/7. . As Operational Scientist in Mammalian production Coordination Team, you will be supporting the production activities related to production and delivery of the needed buffers and media. It is important that you have experience with the processes for preparation of buffer and media in order to provide the right support. The support will be in both technical matters when needed, and in process related subjects. This means, you can master numerus tasks and coordinate these in respect to both the technicians and leaders. In this position, you will have a broad influence and will cooperate with many stakeholders in the entire organization. Production runs 24/7 all year, the position as Operational Scientist is primarily on dayshift, with on call weekend duty, every fourth week. Primary task: Daily coordination with operational scientists from production teams Plan buffer and media preparation for the next day/weekend with team leaders Support when production has questions to buffer/media preparation Support DEV writing related to solutions Participate in planning meetings for projects with project scientist’s and team leaders Contact to project scientist if buffer/media procedures are unclear Ad-hoc approval of buffers There is constant collaboration across the organization, and all employees have a professional and flexible attitude towards their work and to each other. We value good cooperation with a positive attitude. Experience The ideal candidate holds an MSc in Engineering/downstream purification or Biochemistry or similar and experience within the production area in the pharmaceutical industry. The ideal candidate for the position has several of the below competencies/experiences 3 years of experience in the pharmaceutical industry working in an GMP environment Solid knowledge in working with preparation of buffers and media Scientific downstream/purification understanding Strong communication skills (English) Strong collaboration skills LEAN oriented Can cope with a high work pace in a dynamic environment Structured and analytical oriented Flexible As a person you are highly motivated with a strong sense of urgency, a positive “can do” attitude and not afraid of taking responsibility for your tasks or together with stakeholders. AGC Biologics offers a dynamic working place with good opportunities of working with a varied array of tasks and challenges. This opens many doors for personal development and for you to make a real difference towards both patients and customer. At AGC Biologics, the work environment is informal, and humor is part of the work day. We respect each other and our differences, and we help each other to reach deadlines together as one team. We will process the applications as they arrive. Therefore, please submit our resume and application as soon as possible. Want to keep posted about our growth and to learn more about our company? We also urge you to follow us on our LinkedIn Company Page and give us a quick Like on Facebook ! 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. Visit www.agcbio.com to learn why AGC Biologics is a World Leader in process development and contract manufacturing. 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.