Manufacturing Associate, Bulk Drug Substance Upstream - Days

About this role

Career Category Manufacturing Job Description HOW MIGHT YOU DEFY IMAGINATION?  

You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.  

Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX Batch facility will combine the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.  

Manufacturing Associate, Bulk Drug Substance Upstream - Days 

Live  

What you will do  

Let’s do this! Let’s change the world! In this dynamic role, you will be an Associate in the manufacturing organization at Amgen North Carolina (ANC) supporting the facility expansion program and facility startup . This essential role will be part of a team responsible for manufacturing cell culture operations   including seed train, SUBs, Perfusion, RTF, Stainless Steel BRXs, Depth Filtration and Centrifugation,   while partnering across functions to ensure successful operational readiness, technology transfer, and ramp ‑ up of manufacturing operations within the new facility.    

This role may require work outside standard business hours, including non ‑ standard shifts, as needed to support startup, commissioning and qualification (C&Q), and engineering execution.   During this phase of the startup, you will be expected to  work  a Monday – Friday schedule from 8am – 5 pm.   As the business moves from C&Q to manufacturing operations, this essential position   will   work on   a 12-hour 2-2-3 schedule from 5:45 am to   6:15pm   supporting our critical 24/7 manufacturing operations.    As Amgen relies upon the regular attendance of all staff members to meet legitimate business needs, th is role must be able to work assigned 12-hour   shift, including during inclement weather, some holidays and requested overtime in support of our operations.  

During early phases, this role will focus on operational readiness, training, and startup execution. As the facility transitions to steady state operations, the role will shift toward routine manufacturing execution and continuous improvement.  

With general direction, the Associate will support all floor operations in accordance with cGMP practices.  

Key Responsibilities  

Compliance & Quality  

• Execute work in accordance with established cGMP procedures and policies, including SOPs, MPs, JHAs, and applicable CFRs  

• Ensure proper gowning and aseptic techniques are consistently followed  

• Initiate and document manufacturing related deviations and quality events as trained  

• Support investigations and corrective actions under guidance  

• Maintain a strong culture of safety, quality, and compliance  

Operational Readiness & Facility Startup  

• Support operational readiness and facility startup activities as part of the expansion program  

• Participate in training, equipment familiarization, and procedure execution to enable startup  

• Execute assigned readiness tasks supporting commissioning, qualification, and early manufacturing operations  

• Follow defined workflows and procedures to support safe and compliant startup activities  

• Provide operational feedback and escalate issues observed during startup execution  

Manufacturing Operations  

• Perform hands - on manufacturing operations including setup, operation, monitoring, cleaning, and sanitization of equipment and assigned areas  

• Run and monitor critical process tasks per approved procedures  

• Perform in process sampling, operate analytical equipment, and complete Electronic Batch Records (EBRs)  

• Complete washroom activities for small ‑ to large ‑ scale manufacturing equipment  

• Identify and escalate operational issues impacting safety, quality, or schedule  

• Maintain an organized, clean, and compliant manufacturing environment  

Win  

What we expect of you  

We are all different, yet we all use our unique contributions to serve patients. The hard-working professionals we seek are team players with these qualifications.  

Basic Qualifications:  

• High School/GED + 2 years manufacturing and/or other regulated environment experience  

Or  

• Associate’s Degree + 6 months manufacturing and/or other regulated environment experience  

Or  

• Bachelor’s Degree  

​

Preferred Qualifications:  

• Completion of NC BioWork / BioWorks Certification Program  

• Experience in a regulated industry such as biotechnology or pharmaceutical manufacturing  

• Basic understanding of cGMP manufacturing environments  

• Familiarity with EBR/MES, DeltaV , and electronic quality systems  

• Strong verbal and written communication skills  

• Demonstrated desire to learn, grow, and develop manufacturing skills  

• Ability to work effectively in a team -based manufacturing environment  

​

Thrive  

What you can expect of us  

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.  

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.  

Amgen offers a Total Rewards Plan compris

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