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Amgen

Front Line Manufacturing Manager (Bulk Drug Substance - Downstream) - Night Shift

US - North Carolina - Holly Springs

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hirly's read of this role

Seniority
Lead / management
Country
US
Work mode
On-site / unstated
First seen by hirly
28 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

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. The Amgen FleX Batch facility combines the latest in disposable technologies 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.

Manager Manufacturing (Downstream) - Night Shift

Live

What you will do

Let’s do this. Let’s change the world. In these vital and dynamic roles you will be an on-shift front line manager in manufacturing. The working schedule is based on a day or night shift (12-hour) rotation.

The essential position, which supports our critical 24/7 manufacturing operations, works a 12-hour 2-2-3 schedule from 5:45pm to 6:15am.

As a manufacturing leader you will oversee teams of manufacturing associates with differing levels of experience who will be responsible for the manufacture of GMP drug substances. Through structured on the floor presence, you will champion a safe and compliant production environment. As an active participant and role model in a Lean and continuous improvement culture, the manager will imbed these principles onto the manufacturing floor.

Through your leadership, you will oversee teams in technical, on the floor operations in a biotechnology production operation. In addition, you will support the development of your staff through coaching, hiring, and mentorship.

Font-line Manager will assist in defining area objectives, identifying improvement opportunities, and leading change efforts; effectively directing their team and delivering short- and long-term Amgen Operational goals.

Compliance:

Ensure safe working environment

Ensure Amgen policies are followed, including cGMP and CFR (Code of Federal Regulations) compliance of assigned areas

Evaluate current operating procedures and recommend changes to management to optimize production.

Assure all corporate change control procedures are followed, and Regulatory and QA are notified prior to the changes

Interact with regulatory agencies as needed

Assure proper gowning and aseptic techniques are followed

Staff Supervision:

Engage staff and build relationships of trust and respect while driving team performance and continuous improvement

Recruit, train, evaluate, coach and develop staff

Mentor and coach staff members to live by the Amgen Values

Develop and implement trainings plans and programs, to ensure staff are prepared and compliant

Ensure adherence to production schedule and maintenance activities

Interacts with management in optimizing organizational structure and responsibilities

Ensure plant safety through auditing, evaluations, and cross functional walks

Ensure gowning and aseptic techniques training programs are maintained

Process/Equipment/Facilities:

Demonstrate technical mastery of manufacturing processes

Collaborate with cross-functional teams (i.e., QA/QC, F&E, PPIC, Mfg, PD, Regulatory, etc.) in completing production activities

Develop, implement and assess CAPAs and solutions to complex problems

Responsible for elevating and resolving problems during daily operations

Oversees set up, execution, and completion of critical manufacturing processes/tasks

Administrative:

Interacts with management in planning, developing and maintaining budget

Assist in developing and maintaining department goals

Win

What we expect from you

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

Basic Qualifications

Doctorate degree OR

Master’s degree and 3 years of Manufacturing or Operations experience OR

Bachelor’s degree and 5 years of Manufacturing or Operations experience OR

Associate’s degree and 10 years of Manufacturing or Operations experience OR

High school diploma / GED and 12 years of Manufacturing or Operations experience

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

Preferred Qualifications

Bachelor’s degree in Life Sciences or Engineering

Demonstrated strong leadership skills and technical understanding of biotechnology production operations

Experience in biotechnology or pharmaceutical plant start up

Understanding of downstream purification operation (Column Chromatography, TFF, Viral Filtration, Viral Inactivation)

Previous knowledge and experience within a cGMP environment

5+ years process experience in a cGMP manufacturing facility

3+ years of experience in a production Area Lead, Specialist or Manager role

Strong leadership and teambuilding skills (coaching, mentoring, counseling)

Experience with performance management including performance reviews

Conflict Resolution, analytical problem solving, and project management skills

Thorough understanding of regulatory requirements

Excellent verbal and written communication (technical) skills

Excellent computer skills with Microsoft, EBR/MES, Delta V, Electronic quality systems

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 annual base salary range for this opportunity in the U.S. is provided below.

In addition to the base salary, Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.

A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan

Stock-based long-term incentives

Award-winning time-off plans and bi-annual company-wide shutdowns

Flexible work models, including remote work arrangements, where possible

Apply now for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

#AmgenNorthCarolina

. Salary Range

106,148.00USD -143,612.00 USD

Original posting on Amgen's site ↗

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