Amgen Inc. Posted August 31, 2026

Product Quality Associate Director

Remote, United States Full time
Quality Associate Director
Notify me about similar jobs

Amgen Inc. is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Career Category

Quality

Job 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.

Product Quality Associate Director

What you will do

Let’s do this. Let’s change the world.  Amgen’s corporate Product Quality team is seeking an enthusiastic, highly motivated, and team-oriented leader for the position of Product Quality Associate Director. As Product Quality Associate Director, you will provide technical expertise and leadership within a Product Quality Team. You will engage with Product Quality, International Distribution Quality, Quality Control, Regulatory, Process Development, Quality Assurance and other departments on a variety of activities. Such activities include product filings, program improvements, and investigations associated with product manufacturing, in-process controls, analytical methods, specifications, stability, reference standards, importation testing, change control, regulatory submissions and inspections.

In this role you will serve as the accountable Product Quality Leader, representing Quality on the Product Delivery Team(s) for one or more of Amgen's late-stage or commercial biologics products and provide subject matter expertise to the Product Quality Team(s) to develop, implement, and manage strategies to meet the Product Delivery Team goals. You will provide key input and strategic influence for Product Quality related activities including ownership, authoring and review of GMP and regulatory documents, execution of transactions in relevant GMP systems and product data management including comparability assessments, annual product reviews, and product quality risk assessments. Your contributions will significantly improve initiatives intended to ensure the overall product health.

Primary Responsibilities include the following: 

Ensures Product Quality deliverables are appropriately defined within timelines across the Product Delivery Team.   Deliverables are clear with priorities set based on program guidance.

Coordinates discussion and leads decision making for strategies and activities supported within the Product Quality Team (Quality Assurance, Stability, Process Development, and other functions as needed) for programs they support.

Accomplishes results by leading activities across the product quality team and with cross-functional SMEs for programs they support.

Provide effective, cross-functional Quality leadership, and influence and support program deliverables for late phase and commercial programs, including actions required for the annual product reviews, specifications, comparability, and stability programs; site and method transfers; product quality impact assessments; and author PQ-owned regulatory filing sections and RTQs

Provide subject matter expertise and strategic influence for science and risk-based evaluation of complex process and product quality data, including ability to develop patient-oriented strategies that account for business needs and/or provide novel solutions to complex issues

Amgen offers the opportunity to be at the interface between research, global development and manufacturing to ensure that our molecules become medicines. Many of the technologies we’re employing are not only new to Amgen but are new to the industry as a whole. Help us to pave new roads for helping patients.

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is an individual with these qualifications

Basic Qualifications:

Doctorate degree and 3 years of Quality, Operations, Scientific, or Manufacturing experience OR

Master’s degree and 5 years of Quality, Operations, Scientific, or Manufacturing experience OR

Bachelor’s degree and 7 years of Quality, Operations, Scientific, or Manufacturing experience OR

Associate’s degree and 12 years of Quality, Operations, Scientific, or Manufacturing experience OR

High school diploma / GED and 14 years of Quality, Operations, Scientific, or Manufacturing experience

Preferred Qualifications:

B.S. or advanced degree in chemistry, biochemistry, biology, or a related pharmaceutical sciences field and experience with increasing responsibility in a quality, analytical development, process development, pharmaceutics, regulatory, or manufacturing environment

6+ years working in a regulated environment (either direct GMP or technical support) with experience working with biologic products

1+ year experience with authoring or review of market applications, IND, supplements or similar regulatory documentation

Functional Skills:

Must-Have Skills:

Demonstrate proficiency in oral and written communication of complex information to Product Quality leadership, peers and regulatory agencies

Demonstrate proficiency in knowledge of cGMP and international regulatory expectations

Strong scientific data management and organization skills with attention to detail

Soft Skills:

Analytical and problem-solving skills

Ability to work effectively with global, virtual teams

High degree of initiative and self-motivation

Ability to manage multiple priorities successfully, react quickly to address urgent requests and meet challenging timelines

Team-oriented, with a focus on achieving team goals

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, 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.

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.

. Salary Range

145,241.20USD -196,502.80 USD

Job details

Seniority
Associate Director
Function
Quality
Therapeutic area
Not listed
Location
Remote, United States
Employment type
Full time

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 353 comparable Associate Director Quality roles across 90 biopharma companies.

353Comparable roles tracked
328Currently active
90Companies hiring similar roles
35Countries represented

Salary context

73 of 353 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Quality Assurance Senior Specialist - Statistical Sorting · Lilly $18/hr – $35/hr (≈ $37,482–$72,592/yr)
Peer group range $55,037 – $208,845 (median $163,167)

Where these roles are based

Top locations among the 353 comparable roles

United States127
China32
Ireland25
India23
Japan14
Singapore12

+ 29 more countries

Seniority mix

353 of 353 peers have a known seniority level

Manager182
Senior130
Associate Director41

Therapeutic area mix

1 of 353 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Rare Disease1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Gilead Sciences, Inc. Foster City, United States Associate Director
Same function Same seniority Same country
60%similar
Gilead Sciences, Inc. Foster City, United States Associate Director
Same function Same seniority Same country
60%similar
Gilead Sciences, Inc. Foster City, United States Associate Director
Same function Same seniority Same country
60%similar
Novartis Durham, United States Associate Director
Same function Same seniority Same country
60%similar
Novartis Indianapolis, United States Associate Director
Same function Same seniority Same country
60%similar
Boehringer Ingelheim Ridgefield, Connecticut, United States Associate Director
Same function Same seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Associate Director, Quality Assurance Compliance
Gilead Sciences, Inc. · Foster City, United States · Associate Director
Function Therapeutic area Seniority Country
60%
QA Operations Head (Associate Director)
Novartis · Durham, United States · Associate Director
Function Therapeutic area Seniority Country
60%
Associate Director, Global Quality Risk Management
Biogen · Cambridge, United States · Associate Director
Function Therapeutic area Seniority Country
60%
Aseptic Product Quality Associate Director
AbbVie · North Chicago, IL · Associate Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.