Supervisor, Downstream Manufacturing

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.

JOB SUMMARY

The Supervisor, Downstream Manufacturing oversees day-to-day staff in the execution of production processes for GMP bioprocess operations in Manufacturing, and monitors compliance with established processes and standards.

ESSENTIAL JOB DUTIES/RESPONSIBILITIES 

• Ensures compliance with company quality systems, safety procedures, and other company policies 
• Plan daily activities, priorities, and workflow for the team to adhere to the overall schedule 
• Perform and monitor staff during unit operations based on SOP and batch records in compliance with requirements in the 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 needs and output requirements 
• May coach team members on task and skill proficiency and performance with the 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 

QUALIFICATIONS   

• BS/BA degree with 5+ years of industry experience, or master’s degree with 3+ years of industry experience required.
• Equivalent education and experience may substitute for stated requirements 

Shift

D Shift, Wednesday-Friday (every other Saturday) 6:00 pm-6:30 am

COMPENSATION

$94,000-$129,250

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 foste