Amgen Manufacturing Limited LLC Posted August 10, 2026

Sr Associate Quality Control - Microbiology

Juncos, United States Full time
Quality Senior

Amgen Manufacturing Limited LLC 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. 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.

Sr. Associate Quality Control- Microbiology

What you will do

Let’s do this. Let’s change the world. In this vital role you will perform critical testing and analysis to ensure the quality, safety, and consistency of our products before they reach patients.

Specific responsibilities include but are not limited to:

Perform routine and sophisticated analytical testing with precision and accuracy, ensuring compliance with SOPs and regulatory standards.

Maintain meticulous documentation in systems such as LIMS, CIMS, and LMES, following Good Documentation Practices.

Serve as a subject matter expert on cGMPs and SOPs, mentoring peers and modeling adherence to safety and quality protocols.

Troubleshoot testing issues independently and bring up complex problems to management or technical leads as needed.

Review laboratory results for accuracy and compliance, contributing to data integrity and product quality.

Participate in method validation and verification activities to support the lab’s analytical capabilities.

Manage samples efficiently, ensuring proper handling, tracking, and documentation throughout the testing process.

Support continuous improvement initiatives by identifying inefficiencies and contributing to SOP revisions.

Communicate test results and task updates clearly and concisely to team members and stakeholders.

Demonstrate strong time management by prioritizing tasks, meeting deadlines, and supporting team workload balance.

What we expect of you

We are all different! Yet, we all use our unique contributions to serve patients. The Sr. Associate Quality Control professional we seek is an individual contributor with these qualifications.

Basic Qualifications:

Master's Degree

Or

Bachelor’s Degree + 6 months of Quality and/or Laboratory work experience

Or

Associate’s Degree + 2 years of Quality and/or Laboratory work experience

Or

High school/GED + 4 years of Quality and/or Laboratory work experience

Preferred Qualifications:

Educational background in Microbiology, Biotechnology or Medical Technologies.

Laboratory experience in a GMP environment within the Pharmaceutical and/or Biotech industry

Good communications and presentation skills in English and Spanish

Project management skills

Strong organizational skills, including ability to follow assignments through to completion

Enhanced skills in leading, influencing and negotiating

Knowledge of and experience with processes involved in manufacturing and distribution, QA, QAL, validation and process development

Basic Knowledge and skills of word processing, presentations, and spreadsheet applications

Available to support non-standard shift (including 1st, 2nd, 3rd and weekend shifts)

Ability to understand, apply, and evaluate basic chemistry, biology, physical principles and mathematics

Ability to adhere to regulatory requirements, written procedures and safety guidelines

Evaluate documentation/data according to company and regulatory guidelines

to organize work, handle multiple priorities and meet deadlines

Written and oral communication skills

Technical writing capabilities

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.

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 & vision coverage, and life & disability insurance

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.

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.

.

Job details

Seniority
Senior
Function
Quality
Therapeutic area
Not listed
Location
Juncos, 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 136 comparable Senior Quality roles across 35 biopharma companies.

136Comparable roles tracked
125Currently active
35Companies hiring similar roles
21Countries represented

Salary context

34 of 136 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
Peer group range $98,050 – $219,500 (median $147,075)

Where these roles are based

Top locations among the 136 comparable roles

United States72
India15
Ireland13
Singapore10
United Kingdom4
China's Mainland3

+ 15 more countries

Seniority mix

136 of 136 peers have a known seniority level

Senior96
Associate Director26
Principal14

Therapeutic area mix

0 of 136 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

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
AbbVie Irvine, CA Senior
Same function Same seniority Same country
60%similar
AbbVie San Francisco, CA Senior
Same function Same seniority Same country
60%similar
Gilead Sciences, Inc. La Verne, United States Senior
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Renss, United States Senior
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Renss, United States Senior
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Rensselaer, United States Senior
Same function Same seniority Same country

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%
Senior R&D Quality Officer, Product Development Quality Assurance
AbbVie · Irvine, CA · Senior
Function Therapeutic area Seniority Country
60%
Sr QA Validation Specialist (Oversight)
Regeneron Pharmaceuticals, Inc (USA) · Renss, United States · Senior
Function Therapeutic area Seniority Country
60%
Senior Specialist, Quality Assurance Lot Disposition
JuN - Seattle Dexter · Bothell, United States · Senior
Function Therapeutic area Seniority Country
60%
Senior Scientist, Drug Product Analytical Science (ASAT), Cell Therapy
JuN - Seattle Dexter · Seattle 400 Dexter, United States · Senior
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.