Downstream Manufacturing Associate III/Senior (WA)

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 role of the Manufacturing Associate is to act as a controller, providing essential duties to support the respective production suite, Supervisor, and Manager. On a daily basis, the Manufacturing Associate is expected to have a full understanding of the schedule and required tasks; promoting adequate assessment and response of any production demands.

An Associate III performs bioprocess operations in Manufacturing in compliance with established processes and standards. 

An Associate Senior leads multidisciplinary teams on manufacturing projects and is responsible for implementing and troubleshooting bioprocess operations in compliance with established processes and standards.  

ESSENTIAL JOB DUTIES/RESPONSIBILITIES – Associate III

• Responsible for bioprocess operations (filtration, protein purification, chromatography/separation, viral inactivation/UFDF, bulk fill) as well as CIP/SIP operations (cleaning, assembly, sterilization, disassembly, and operation)
• Complete processing documentation (product changeover, etc.)
• Create, review, and revise GMP documentation (SOPs)
• Recommend and execute projects and bioprocess operation improvements to reduce risk and increase efficiency
• Train others in bioprocess operations and documentation practices
• Participate in compliance and technical development projects
• Supports or may lead multiple more complex projects/initiatives/work items under broad supervision
• Analyzes issues and makes decisions based on standardized processes and procedures in collaboration with relevant stakeholders
• Communicates moderately complex concepts and interacts with others to inform and direct action
• Acts as a resource for less experienced team members and colleagues
• Demonstrates knowledge of equipment and technology

LEADERSHIP SKILLS – Associate III

• Analyzes multiple sources of information and evaluates several alternative solutions before confirming the correct path
• Explains complicated information and effectively lays out variations of alternatives to consider
• Works across teams effectively
• Applies understanding of how the team relates to other closely related areas to improve efficiency of own team
• Understands and complies with AGC Code of Conduct and is a role model to others

ESSENTIAL JOB DUTIES/RESPONSIBILITIES – Associate Senior

• Participate in and troubleshoot bioprocess operations (filtration, protein purification, chromatography/separation, viral inactivation/UFDF, bulk fill) as well as CIP/SIP operations (cleaning, assembly, sterilization, disassembly, and operation)
• Review and revise GMP documentation (SOPs)
• Recommend and implement bioprocess operation improvements to reduce risk and increase efficiency
• Set up training and development for compliance requirements and departmental policies
• Set up troubleshooting activities on bioprocess operations
• Participate in compliance and technical development projects
• Develops and leads large and/or multiple programs, initiatives, and activities for the function or broad organization with moderate resource requirements, risk, and/or complexity
• Analyzes and evaluates issues and makes decisions within general parameters under little supervision
• Contributes to the development of best practices for functional area
• Communicates complex concepts and interacts with others to inform and direct action
• Acts as a "go-to" resource in area of expertise
• Demonstrates in-depth knowledge of equipment and technology

LEADERSHIP SKILLS – Associate Senior

• Leads others to solve complex problems; uses sophisticated analytical thought to exercise judgment and identify appropriate solutions
• Explains difficult or sensitive information and works to build consensus and is building a skill set to persuade others
• Understands and complies with AGC Code of Conduct and is a role model to others

REQUIRED QUALIFICATIONS  

• Associate III - BS/BA degree and years of relevant experience. Equivalent education and experience may substitute for stated requirements 
• Associate Sr. - BS/BA degree and 5 years of relevant experience. Equivalent education and experience may substitute for stated requirements 

HOURS  

Associates work a 3-4 schedule (three 12-hour shifts in week one and four 12-hour shifts in week two). Our Manufacturing team has four shifts. Night shifts are eligible for shift differential.

• A Shift: Su-Tu (We) 6:00-18:30
• B Shift: Su-Tu (Sa) 18:00-6:30
• C Shift: Th-Sa (We) 6:00-18:30
• D Shift: We-Fr (Sa) 18:00-6:30

COMPENSATION RANGE

• Associate III - $36.03-$49.55
• Associate Sr. - $40.34-$55.47
   

At AGC Biologics, we are always seeking dedicated and skilled Manufacturing Associates to join our team. By maintaining this evergreen job posting, we can connect with potential candidates as new opportunities arise within our team. We actively monitor applications and continuously match candidates to available positions, ensuring that we find the right fit for both you and our organization.

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.
 

Salary : $36 - $50