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. The role of the Downstream Manufacturing Supervisor is to be responsible for successful, compliant downstream operations. The Downstream Manufacturing Supervisor is expected to work in Good Manufacturing Practice (cGMP) environment, have and expert level of working knowledge of downstream processes, the ability to manage multiple ongoing projects concurrently as well as have excellent meeting facilitation and conflict resolution skills. The Downstream Manufacturing Supervisor is required to be action oriented, and be compliant minded while leading operations. ESSENTIAL JOB DUTIES/RESPONSIBILITIES Ensures compliance with company quality systems, safety procedures, and other company policies Plan daily activities, priorities and workflow for team to adhere to overall schedule Perform and monitor staff during unit operations based on SOP and batch records in compliance with requirements in Quality System Review and ensure errors are corrected during manufacturing operations Train, coach, and mentor manufacturing technicians/associates on manufacturing functions Complete required documentation; review and approve executed manufacturing MBRs Develop staff (i.e. set goals, assign development activities, review performance, etc.) Supervises daily operations for a project/team comprised of support and/or professional employees Provides technical leadership in a specific work area Prioritizes and assigns project goals; ensures tasks are completed and work area goals are met Coordinates with other supervisors and teams to meet the business need and output requirements May coach team members on task and skill proficiency and performance with manager’s guidance LEADERSHIP SKILLS Applies understanding of how the team relates to other related areas to improve efficiency of own team Recognizes performance improvements and conveys feedback constructively Works across teams effectively EDUCATION/EXPERIENCE: BS in Biochemistry, Biology, Chemistry or related field desired. 8 years GMP operations experience, including 3 years leading a team/group. Experience in one or more of the following Bioprocess operations (Cell Culture/Production, Harvest and Recovery, or Purification). Equivalent education and experience may substitute for stated requirements. 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.