Manager Manufacturing Environmental and Contamination Control
AmgenAbout the role
Career Category
OperationsJob Description
Join Amgen’s Mission of Serving Patients
At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.
Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Manager Manufacturing Environmental & Contamination Control
What you will do
Let’s do this. Let’s change the world. In this vital role you will be responsible for day-to-day delivery of deviation records and investigations, ensuring Deviation Owners and FAOs execute with rigor, speed, and compliance, particularly for microbial and EM-related events. This role shall report to the Senior Manager of the Environmental and Contamination Control (ECC) team.
Responsibilities
The Front-Line Manager
Direct Management of Deviation Owners & FAO's
Lead and coordinate:
Deviation Owners (execution)
Process Specialists (technical oversight)
Ensure:
Clear ownership assignment and appropriate planning and distribution of workload
Timely movement of records
Deviation Lifecycle Execution
Oversee: Initiation → triage → investigation → closure
Ensure records are complete, accurate, and audit-ready
Remove barriers to timely closure and escalation
Investigation Quality Oversight
Ensure:
Robust root cause analysis (RCA)
Appropriate scoping and impact assessment
Challenge teams to avoid superficial or convenience-based conclusions
Microbial Event Execution (Critical Focus)
Ensure microbial deviations receive appropriate SME engagement (QC Micro, aseptic SMEs)
Verify:
Investigations reflect true contamination risks
Classification reflects risk (not bias or precedent)
Decision Facilitation & Alignment
Facilitate alignment between:
FAO
QA
Deviation Owner
Ensure decisions (classification, disposition) are clearly documented
CAPA Execution & Follow-Through
Ensure CAPAs are:
Assigned
Owned
Completed effectively
Confirm clear linkage between root cause and actions
Triage & Prioritization
Lead daily deviation triage for environmental and contamination control-related events
Prioritize high-risk (e.g., microbial, major deviations)
Ensure effective tools and business processes are in place for tracking and reporting record progress
Allocate resources appropriately
Inspection Readiness Support
Prepare team to:
Speak to deviations directly
Defend scientific rationale
Ensure records are inspection-ready at all times
Continuous Improvement
Create a culture of continuous improvement among the ECC team and facilitate implementation of tools and processes that streamline the investigation process, making appropriate use of AI and other digital tools.
Key Performance Metrics
On-time closure (OTD)
Aging backlog
Investigation effectiveness
CAPA cycle time
Audit/inspection observations
All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional tasks and responsibilities.
What we expect of you
We are all different, yet we all use our unique contributions to serv
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