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West Greenwich, Rhode Island, United States
Hybrid
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 yourSr. Engineer, F&E Environmental & Contamination Control
Sr. Engineer, F&E Environmental & Contamination Control
What you will do
Let’s do this. Let’s change the world. In this vital role you will report to the Facilities & Engineering organization and serve as a technical deviation owner or Functional area owner responsible for investigating and resolving equipment, utility, automation, facility, commissioning, qualification, and project-related quality events.
The Engineering Deviation Owner and/or functional area owner is accountable for the end-to-end management of assigned deviation records, ensuring investigations are technically sound, scientifically justified, inspection-ready, and completed in accordance with site procedures and regulatory expectations.
Responsibilities
Deviation Ownership & Execution
Demonstrated technical writer capable of translating complex engineering, equipment, automation, utility, and project-related events into concise, technically accurate, and inspection-ready documentation.
Independently drive deviation investigations from initiation through closure while ensuring compliance with site procedures and quality system requirements.
Maintain accountability for record quality, data integrity, technical accuracy, and timely progression of assigned deviations.
Prioritize and manage multiple investigations simultaneously in a dynamic manufacturing environment.
Technical Investigation & Root Cause Analysis
Develop and execute investigation strategies for equipment, utility, facility, automation, commissioning, qualification, and manufacturing support events.
Conduct field assessments, equipment walkdowns, system reviews, and Genba activities to gather factual evidence.
Utilize engineering problem-solving methodologies to determine root cause and contributing factors.
Lead structured Root Cause Analysis (RCA) sessions involving cross-functional stakeholders.
Evaluate potential impacts to validated systems, product quality, operational reliability, and compliance.
Corrective and Preventive Actions (CAPA)
Develop technically robust corrective and preventive actions aligned with investigation outcomes.
Ensure CAPAs address both immediate causes and systemic contributors.
Support effectiveness verification activities and long-term monitoring strategies.
Identify opportunities to improve equipment reliability, utility performance, maintenance practices, and engineering processes.
Cross-Functional Collaboration
Partner with Manufacturing, Quality Assurance, Quality Control, Automation, Maintenance, Facilities, Engineering Technical Authorities (ETA), Process Development, Capital Projects, and Global Engineering organizations.
Facilitate alignment among stakeholders and drive timely technical decision-making.
Ensure appropriate SME engagement and challenge assumptions through data-driven discussions.
Documentation & Technical Decision Making
Develop investigation narratives and technical assessments that clearly communicate event chronology, causal analysis, risk assessments, and conclusions.
Support impact assessments associated with:
Equipment modifications
Utility system changes
Automation updates
Commissioning and qualification activities
Capital project implementation
Ensure documentation meets Quality Management System (QMS) requirements and inspection expectations.
Regulatory & Inspection Readiness
Serve as a Subject Matter Expert (SME) during regulatory inspections and internal audits for assigned investigations.
Defend technical conclusions, investigation rationale, and risk-based decisions.
Support inspection preparation activities and response development as needed.
Data Analysis & Continuous Improvement
Analyze deviation trends associated with:
Equipment reliability
Utility performance
Automation systems
Facility infrastructure
Commissioning and qualification activities
Identify recurring issues and opportunities for systemic improvement.
Leverage digital tools, data analytics, AI-enabled technologies, and engineering metrics to improve investigation efficiency and effectiveness.
Contribute to site initiatives focused on reliability, operational excellence, and inspection readiness.
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is a self-starter with these qualifications.
Basic Qualifications
High school diploma / GED and 10 years of Engineering, Facilities, Manufacturing, Automation, CQV, Quality, or related experience OR
Associate's degree and 8 years of Engineering, Facilities, Manufacturing, Automation, CQV, Quality, or related experience OR
Bachelor's degree and 4 years of Engineering, Facilities, Manufacturing, Automation, CQV, Quality, or related experience OR
Master's degree and 2 years of Engineering, Facilities, Manufacturing, Automation, CQV, Quality, or related experience OR
Doctorate
Preferred Qualifications
BS/BA in Engineering, Life Sciences, Biotechnology, Chemistry, or related discipline
5+ years of experience in pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments
Experience with:
Facilities & Engineering systems
Equipment troubleshooting
Utility systems
Automation systems (DeltaV, BAS, PI)
Commissioning & Qualification (C&Q)
Root Cause Analysis methodologies
Change Control and Quality Systems
Strong technical writing and analytical problem-solving skills
Ability to influence and lead cross-functional teams without direct authority
Experience applying AI, analytics, or digital tools to support investigations and continuous improvement
What you can expect from us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.
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.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of 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 that may include:
A 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
Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.
Apply now and make a lasting impact with the Amgen team.
careers.amgen.com
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
Sponsorship for this role is not guaranteed.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
.Salary Range
115,494.60USD -156,257.40 USD