Amgen

Senior Manager: Manufacturing - Downstream Bulk Drug Substance

Amgen  •  Holly Springs, NC (Onsite)  •  2 hours ago
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Job Description

Career Category

Manufacturing

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. The Amgen FleX Batch facility combines the latest insingleusetechnologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. The FleX Batch facility not only features the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it also integrates sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027. 

Senior Manager: Manufacturing- Downstream Bulk Drug Substance

Live

What you will do

Let’sdo this.Let’schange the world. As Senior Manager of Manufacturing, you will provide leadership and guidance to the team responsible for 24/7 manufacturing operations in downstream purification.

In this vital role as a member of the Manufacturing Leadership Team, the Senior Manager of Manufacturing will collaborate cross-functionally to enable the commissioning, qualification, start-up, and GMP operation of a new drug substance manufacturing facility. This roleis responsible forcoaching and developing Downstream Front-Line Managers who oversee staff supporting direct drug substance production.

The Senior Manager will be accountable for the organizational design of the manufacturing team, including workforce planning, hiring, onboarding, training, qualification, and development of staff to support safe, reliable, and compliant operations. The role will ensure that personnel are appropriately trained and qualifiedin accordance withestablished training programs, procedures, and operational readiness requirements.

The position will provide leadership and manufacturing oversight for Commissioning and Qualification activities associated with downstream process systems, equipment, utilities, and supporting infrastructure. Responsibilities will include partnering with Engineering, Quality, Automation, Validation, Process Development, and project teams to review system designs, commissioning and qualification protocols, acceptance criteria, turnover packages, and supporting documentation to confirm that systems are safe, compliant, maintainable, and operationally ready.

The Senior Manager will ensureappropriate Manufacturingparticipation in design reviews, system walkdowns, factory and site acceptance testing, commissioning execution, equipment qualification, process demonstrations, water runs, engineering runs, and performance qualification activities. The role will also support the identification, documentation, escalation, and resolution of equipment, process, automation, and facility issuesidentifiedduring C&Q and start-up. The position will also provide leadership and oversight for downstream chromatography column packing activities to ensure readiness for reliable GMP operations.

Additionally, the Senior Manager will lead operational readiness activitiesrequiredfor successful facility start-up and transition to routine GMP manufacturing. This includes development and execution of readiness plans, establishment of operating procedures and standard work, completion of training and qualification activities, confirmation of materials and equipment availability, implementation of shift structures, and verification that manufacturing systems and support processes are prepared for operation.

The position willestablishand monitor readiness metrics, risks, dependencies, and action plans, ensuring that gaps areidentifiedearly, assigned to accountable owners, and resolved in alignment with project and manufacturing milestones. The Senior Manager will also ensure effective handover of qualified systems from the project organization to Manufacturing andestablishsustainable processes for equipment ownership, system performance monitoring, troubleshooting, preventive maintenance coordination, and continuous improvement.

Following facility start-up, the Senior Manager will be accountable for sustained manufacturing performance, including safety, quality, compliance, schedule adherence, operational reliability, workforce capability, and continuous improvement across downstream purification operations.

Responsibilities:

  • Develop andretaina diverse and high performing team in alignment with operational readiness schedules to ensure successful startup and commercial GMP operations

  • Mature the site’s safety and quality culture of the department and champion continued improvement

  • Collaborate as one team of all manufacturing support groups (Quality, Process Development, Engineering, Supply Chain, and network partners)

  • Provide support to troubleshoot,identify, and resolve issues as needed and manage call coverage for 24/7 operation

  • Provide technical leadership for the investigation of deviations and the development of corrective actions

  • Develop and implement departmental strategy and plans that are aligned with the broader organizational strategy and deliver continuous improvement

  • Provide leadership and oversight for downstream chromatography column packing activities, including planning, execution, qualification, troubleshooting, documentation, and readiness to support reliable GMP manufacturing operations.

  • Lead and support regulatory inspections for areas of responsibilities including evaluating complex compliance issues and developing playbooks for the inspections

  • Deliver against organizational financial commitments while championing a lean philosophy

  • Provide Manufacturing leadership and support for Commissioning and Qualification activities, including design reviews, system walkdowns, protocol execution, issue resolution, and equipment turnover

  • Lead operational readiness activities for downstream manufacturing, including procedures, training, staffing, materials, system ownership, and readiness assessments to support successful facility start-up and transition to GMP operations.

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The experienced professional we seek is a collaborative partner with these qualifications. 

Basic Qualifications:

Doctorate degree and 2 years of Manufacturing & Operations experience Or 

Master’s degree and 6 years of Manufacturing & Operations experience Or 

Bachelor’s degree and 8 years of Manufacturing & Operations experience Or 

Associate's degree and 10 years of Manufacturing & Operations experience Or 

High School diploma/GED and 12 years of Manufacturing & Operations experience  

AND 2 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources 

Preferred Qualifications

  • Demonstrated managerial experience in a GMP manufacturing drug substance plant 

  • Demonstrated experience in applying Operational Excellence and Lean Manufacturing 

  • Cross-functional work experience in either Process Development, Quality or Engineering 

  • Excellent communication skills, drive, sense of urgency, energyleveland problem-solving abilities 

  • Demonstrated ability to forge andmaintainstrong relationships with other functional areas 

  • Ability to effectively develop and coach staff and positively advance the culture of an organization 

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. 

  • Vast opportunities to learn and move up and across our global organization 

  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act 

  • Generous Total Rewards Plancomprisinghealth, finance and wealth, work/life balance, and career benefits 

Apply now 

for a career that defies imagination 

In our quest to serve patientsabove all else, Amgen is the first to imagine, and the last to doubt. Join us. 

careers.amgen.com 

#AmgenNorthCarolina 

Salary Range

136,227.80USD -184,308.20 USD

Amgen

About Amgen

Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We helped establish the biotechnology industry, and we remain on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. Our investment in research and development has yielded a robust pipeline that builds on our existing portfolio of medicines to treat cancer, heart disease, osteoporosis, inflammatory diseases and rare diseases.

Amgen is one of 30 companies comprising the Dow Jones Industrial Average®, and part of the Nasdaq-100 Index®. In 2024, Amgen was named one of the “World’s Most Innovative Companies” by Fast Company and one of “America’s Best Large Employers” by Forbes.

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Industry
Biotech & Life Sciences
Company Size
10,000+ employees
Headquarters
Thousand Oaks, CA
Year Founded
1980
Website
amgen.com
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