Specialist Manufacturing Environmental and Contamination Control
Specialist Manufacturing Environmental and Contamination Control
US - Rhode Island - West Greenwich Apply NowJoin 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.
Specialist Manufacturing Environmental & Contamination Control
What you will do
Let’s do this. Let’s change the world. In this vital role you will be accountable technical authority for microbial-related deviations (e.g., EM excursions, bioburden, contamination events) within their functional domain, ensuring scientifically robust investigations, risk-based decisions, and effective CAPA implementation aligned to GMP and regulatory expectations.
Responsibilities:
Technical Ownership of Microbial Investigations
Provide functional SME oversight for microbial events, including:
Environmental Monitoring (EM) excursions
Bioburden / endotoxin / contamination signals
Ensure investigations are scientifically sound and microbiologically justified
Ensure true root cause identification with supporting data and rationale
Accountability for Investigation Quality & CAPA
Ensure:
Thorough root cause analysis (RCA)
Appropriate Corrective / Preventive Actions (CA/PA/EV) to prevent recurrence
Validate that:
Each root cause has a corresponding action
CAPAs are effective, risk-based, and sustainable
Decision Authority – Product & Process Risk
Accountable for:
Decision and documented rationale for continued processing or disposition
Collaborate with QA to ensure:
Decisions are defensible, risk-appropriate, and aligned with GMP expectations
Deviation Classification & Designation Support
Contribute to Major vs Minor classification decisions based on impact and controls
Ensure classification reflects true microbiological risk (not convenience or precedent)
Resource & Investigation Oversight
Ensure:
Appropriate SME engagement (e.g., Microbiology, QC, MFG)
Adequate resources are deployed to support investigation depth
Cross-Functional Integration (Critical for Microbial Events)
Work closely with:
QC Microbiology (EM data interpretation)
Manufacturing (aseptic behavior, execution)
QA (final decision authority)
Embedded within ECC model with dedicated microbial expertise and deviation FAO support
Own the ECC genba program and ensure cross-functional participation, effective engagement, and actionable outcomes
Engagement Across Deviation Lifecycle
Maintain active involvement from triage through closure
Ensure:
Timely decisions
Strong documentation
Alignment across stakeholders
Inspection Readiness & Defense
Act as key spokesperson during inspections for microbial events
Must:
Clearly articulate root cause
Defend classification rationale
Demonstrate CAPA effectiveness
Key Differentiators – Microbial FAO vs Standard FAO
Demonstrate Microbial science depth
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 serve patients. The dedicated professional we seek is a self-starter with these qualifications.
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The [vital attribute] professional we seek is a [type of person] with these qualifications.
Basic Qualifications
High school diploma/GED and 10 years of directly related experience OR
Associates degree and 8 years of directly related experience OR
Bachelor’s degree and 4 years of directly related experience OR
Master’s degree and 2 years of directly related experience OR
Doctorate degree
Preferred Qualifications
The knowledge and skills necessary to perform the duties of this position are typically acquired through the following combination of education and experience or the equivalent
BS/BA or equivalent (Microbiology/Life Science)
8+ years of Microbiology industry experience in the pharmaceutical industry
Experience applying AI or other digital tools to generate insights and streamline workflows
Strong understanding of GxP and deviation management processes and Microbiology / contamination control principles
Ability to apply risk-based decision making, influence cross-functional teams & communicate clearly under inspection pressure
Strong understanding of EM program design and limitations, objectionable organisms & contamination pathways and aseptic processing risk
Knowledge of network and industry trends in managing and responding to microbial contamination risk
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.
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Application deadline
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
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.