Manager ManufacturingProgramsInvestigations

BioSpace

Holly Springs (NC)

On-site

USD 120,000 - 180,000

Full time

14 days+
Application generator

A complete application in a minute — tailored resume and cover letter, ready to send.

Get past ATS filters

Benefits offered by this job

Health and welfare benefits
Annual bonus opportunity
Stock-based long-term incentives
Generous paid time off

Job summary

Amgen is seeking a Manager Manufacturing Programs Investigations in the United States. You will lead a team of Manufacturing Investigation Specialists, applying advanced microbiology and environmental monitoring principles to support investigations.

You will build a safe, inclusive culture while driving root-cause analysis and CAPA across functions. You will collaborate with Manufacturing, Quality, Engineering, Automation, EHSS, and Process Development, oversee governance for deviations, and

Qualifications

  • Doctorate or Master’s with related experience or equivalent
  • Bachelor’s with 5+ years of related experience; Associate’s with 10+ years; High school with 12+ years
  • Experience directly managing people or leadership of teams/projects/prograns, or resource allocation

Responsibilities

  • Lead, develop, coach, and mentor a team of Manufacturing Investigation Specialists
  • Apply microbiology and environmental monitoring knowledge to support investigations
  • Create an environment of psychological safety and encourage diverse perspectives
  • Manage team priorities, workload, and performance
  • Provide technical oversight of manufacturing and environmental monitoring investigations
  • Drive root-cause analysis and CAPA development
  • Serve as site subject matter expert for Environmental Monitoring investigations
  • Lead cross-functional partnerships across Manufacturing, Quality, Engineering, Automation, EHSS, and Process Development
  • Lead escalation and governance for deviations
  • Support regulatory inspections and internal audits
  • Monitor investigation metrics and drive continuous improvement
  • Champion Operational Learning Team principles
  • Develop investigation procedures, standards, and training
  • Build a culture of accountability, inclusion, and operational excellence

Skills

People leadership
Cross-functional collaboration
GMP knowledge
Environmental monitoring
Root cause analysis
Problem solving
Coaching

Education

Doctorate degree
Master's degree
Bachelor's degree
Associate's degree

Tools

Veeva QMS

Job description

HOW MIGHT YOU DEFY IMAGINATION?

If you feel likeyourepart of something bigger,itsbecause you are. At Amgen, our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies. We are global collaborators who achieve togetherresearching, manufacturing, anddeliveringever-better products that reach over10 million patientsworldwide.Itstime for a career you can be proud of.

Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the AmgenFleXbatch facility will combine the latest in single use technologies with traditional stainless steel equipment to allow for maximum flexibility in operations TheFleXBatch 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.

Manager Manufacturing Programs Investigations
What Youwill Do
  • Lead, develop, coach, and mentor a team of Manufacturing Investigation Specialistsspecializing in simple deviation and environmentalmonitoringinvestigations.
  • Applyadvancedunderstanding of microbiology principles, environmental monitoring programs, and contamination control strategies to support environmental monitoring investigations.
  • Create an environment of trust and psychological safety where team members feel empowered to raise concerns, challenge assumptions, share diverse perspectives, and contribute openly to problem-solving discussions.
  • Manage team priorities, workload balancing, resource planning, and performance management.
  • Provide technical oversightofmanufacturing and environmental monitoring investigations.
  • Drive consistency in root cause analysis and CAPA development.
  • Serve as site subject matter expert forEnvironmental Monitoringrelatedinvestigations.
  • Lead cross-functional partnerships across Manufacturing, Quality, Engineering, Automation, EHSS, and Process Development.
  • Lead escalation and governance fordeviations.
  • Supportand present duringregulatory inspections and internal audits.
  • Monitorinvestigationmetrics and drive continuous improvement.
  • Champion Operational Learning Team principles and organizational learning.
  • Develop investigation procedures, standards, and training.
  • Build a culture of accountability, inclusion, and operational excellence.
What We Expectof you

The collaborative leader weseekhas extensivebiologicsdrug substance manufacturing experience withdemonstratedsuccess leading technical teams, driving cross-functional collaboration, and improving quality systems.

Basic Qualifications
  • Doctorate degree
  • Master'sdegreeand3years ofdirectly relatedexperience
  • ORBachelor'sdegree and 5 years ofdirectly relatedexperience
  • ORAssociate'sdegree and 10 years ofdirectly relatedexperience
  • OR High school diploma/GED and 12 years ofdirectly relatedexperience
  • In addition to meeting at least one of the above requirements, you must have experience directly managing people and/or leadership experience leadingteams, projects,prograns, or directing the allocationorresources.Your managerial experience may run concurrently with the required technical experience referenced above
Preferred Qualifications
  • 5+ years ofbiologicsmanufacturing, microbiology, quality, or related pharmaceutical experience.
  • 0-2years ofpeopleleadership or technical leadership.
  • Strong knowledge of GMPs, contamination control, and environmental monitoring.
  • Expertiseleading investigations and root cause analysis.
  • Degree in Science or Engineering(Microbiology or similara plus).
  • Experience with Veeva QMS or equivalent quality systems.
  • Experience supporting FDA and global regulatory inspections.
  • Strong communication, coaching, and organizational leadership skills.

The annual salary range for this opportunity in the U.S. is [HR to input market pay range].

In addition to base salary, Amgen offers a comprehensive Total Rewards package including

  • health and welfare benefits
  • retirement savings
  • annual bonus opportunity
  • stock-based long-term incentives
  • generous paid time off
  • company shutdowns
  • career development opportunities
Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Manager Manufacturing Programs – Investigations
Manager Manufacturing Programs – Investigations

Amgen • Holly Springs (NC)

On-site
USD 120,000 - 180,000
Manager Manufacturing Programs – Investigations
Manager Manufacturing Programs – Investigations

Biopharma Careers • Holly Springs (MS)

On-site
USD 120,000 - 160,000
Manager Manufacturing Programs - Investigations
Manager Manufacturing Programs - Investigations

Amgen SA • Holly Springs (NC)

On-site
USD 180,000 - 240,000
Specialist Manufacturing Investigations
Specialist Manufacturing Investigations

NCBiotech • Holly Springs (NC)

On-site
USD 107,000 - 146,000
Comprehensive employee benefits package
Retirement and savings plan
Flexible work models
Senior SpecialistInvestigations & Regulatory Inspections
Senior SpecialistInvestigations & Regulatory Inspections

BioSpace • Holly Springs (NC)

Hybrid
USD 140,000 - 180,000
Senior Specialist – Complex Investigations
Senior Specialist – Complex Investigations

Amgen • Holly Springs (NC)

Hybrid
USD 120,000 - 170,000
Retirement plan
Medical, dental, vision
Yearly bonus
+3
Senior Manager Manufacturing - Deviation Investigations
Senior Manager Manufacturing - Deviation Investigations

BioSpace • Holly Springs (NC)

On-site
USD 180,000 - 230,000
Competitive salary
Comprehensive Total Rewards Plans
Equal opportunity employer
+1
Senior Specialist Complex Investigations
Senior Specialist Complex Investigations

Amgen SA • Holly Springs (NC)

On-site
USD 120,000 - 160,000
Retirement plan
Medical coverage
Life insurance
+6
Senior Associate Manufacturing - Technical Training - Upstream Bulk Drug Substance
Senior Associate Manufacturing - Technical Training - Upstream Bulk Drug Substance

Amgen SA • Holly Springs (NC)

Hybrid
USD 90,000 - 120,000
Retirement plan
Medical, dental & vision
Discretionary bonus
+2
Front Line Manufacturing Manager (Bulk Drug Substance - Downstream) - Day Shift
Front Line Manufacturing Manager (Bulk Drug Substance - Downstream) - Day Shift

Amgen SA • Holly Springs (NC)

On-site
USD 80,000 - 100,000
Comprehensive benefits package
Retirement savings plan
Flexible work models