Senior Director Quality Assurance
Company: Amgen
Location: West Greenwich
Posted on: January 6, 2026
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Job Description:
Join Amgens Mission of Serving Patients At Amgen, if you feel
like youre part of something bigger, its because you are. Our
shared missionto serve patients living with serious illnessesdrives
all that we do. Since 1980, weve helped pioneer the world of
biotech in our fight against the worlds toughest diseases. With our
focus on four therapeutic areas Oncology, Inflammation, General
Medicine, and Rare Disease we reach millions of patients each year.
As a member of the Amgen team, youll 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, youll thrive as part of the
Amgen team. Join us and transform the lives of patients while
transforming your career. Senior Director, Quality Assurance What
you will do Lets do this. Lets change the world! By taking on this
leadership role, you will have the opportunity to augment the
future and contribution of Quality Operations at Amgen Rhode Island
(ARI) through the advancement of Amgens pipeline and diversified
portfolio from our state-of-the-art Drug Substance manufacturing
site located in West Greenwich. In this vital role, you will be
responsible for actively driving operational workstreams. You will
provide Quality leadership and guidance to site partners as we
continue to grow and deliver our mission of "Every patient, Every
Time." Your responsibilities also extend to the integration of
technology in our daily activities to ensure effective and
efficient tech transfer, as well as maintaining compliant ongoing
operations. As the Senior Director Quality Assurance providing
oversight to two (2) manufacturing facilities, you will contribute
to the development of the site Quality strategy and build and lead
a team of approximately 50 associates accountable for all aspects
of quality oversight of GMP manufacturing processes. This role will
ensure product quality standards are met in compliance with Amgen
and regulatory requirements. Responsibilities: Lead Plant QA team
providing Quality Oversight of 24/7 continuous manufacturing
operation and high impact strategic decision making in two (2)
multi-product Drug Substance facilities (14 products) with
accelerated run rate and expansion projects to support volume
driven growth and innovative pipeline. Scope includes on-the-floor
support for AR5 Fed batch and AR30 MoF, I-530, Buffer Preparation
Area, Media Preparation, Component Preparation Area, In Process
Testing Lab, record review, quality oversight of deviation
investigations and changes, document approval, and disposition.
Ensure drug substance is manufactured, tested, stored, and
distributed according to current Good Manufacturing Practices
(cGMP), Amgen standards, and other applicable regulations and
specifications. Provide oversight to ensure that Amgen Quality
Management System is implemented and maintained in accordance with
corporate standards. Track performance and drive continuous
improvement in the performance and delivery of quality outputs in
alignment with Quality strategies. Provide quality input and
partner with cross-site and cross-functional area leads to advance
Amgens manufacturing strategy. Develop strategies in support of
regulatory inspections and site audits. Serve as quality
representative to regulatory authorities, Amgen Corporate auditors,
and 3rd Parties. Develop area budget, manage expenditure and
identify productivity improvement opportunities. Represent ARI
Quality in cross-function and cross-site forums. Provide Quality
input to support project or operational design decisions. Alert
management of significant quality, compliance, supply, and safety
risks. Communicate across all levels of the organization.
Facilitate development of solutions to critical business issues.
What we expect of you We are all different, yet we all use our
unique contributions to serve patients. The Quality professional we
seek is a Leader with these qualifications. Basic Qualifications:
Doctorate degree and 4 years of Quality/Manufacturing/Engineering
experience OR Masters degree and 8 years of
Quality/Manufacturing/Engineering experience OR Bachelors degree
and 10 years of Quality/Manufacturing/Engineering experience And In
addition to meeting at least one of the above requirements, you
must have at least 5 years experience directly managing people
and/or leadership experience leading teams, projects, programs, or
directing the allocation or resources. Your managerial experience
may run concurrently with the required technical experience
referenced above Preferred Qualifications: Bachelors Degree in a
Life Science field 15 years pharmaceutical industry experience
Previous experience in Quality oversight of Biologics drug
substance operations Strong knowledge of cGMPs and experience
interacting with Regulators Able to drive process improvement
within area of responsibility Able to successfully manage workload
to timelines Leadership and communication skills What you can
expect of 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, well 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. 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.
Keywords: Amgen, Hartford , Senior Director Quality Assurance, Science, Research & Development , West Greenwich, Connecticut