Sr Associate Quality Control - Microbiology
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.
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Job details
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.
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.
Where these roles are based
Top locations among the 136 comparable roles
+ 15 more countries
Seniority mix
136 of 136 peers have a known seniority level
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.
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.
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.