New · posted Nov 10
Amgen · Biotechnology
Associate Quality Control HPLC/CE
- Thousand Oaks, CA
- On-site
- Full-time
- Associate & Specialist
The role
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. Amgen is advancing a broad and deep pipeline and portfolio of medicines to treat heart disease, obesity and obesity-related conditions, rare diseases, inflammatory conditions and cancer. 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.
What you need
Basic Qualifications
Bachelor’s degree OR Associate’s degree and 6 months of Quality Control, Quality Assurance or related experience OR High school diploma / GED and 2 years of Quality Control, Quality Assurance or related experience
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 employee with these qualifications.
Preferred Qualificationsnice to have
- Experience in HPLC and/or Capillary Electrophoresis techniques
- Ability to adhere to regulatory requirements, written procedures and safety guidelines
- Ability to evaluate documentation/data according to company and regulatory guidelines
- Ability to organize work, handle multiple priorities and meet deadlines
- Strong written and oral communication skills
- Must be detail orientated
- Must be flexible and adaptable to changing priorities and requirements
- Demonstrate understanding of regulatory requirements, safety guidelines and factors impacting compliance
- Demonstrate understanding of when and how to appropriately escalate
What you'll do
Let’s do this. Let’s change the world.
The Associate Quality Control will support the QC analytical chemistry team by performing testing HPLC/UHPLC (high and ultra-high liquid chromatography), titer, CE (capillary electrophoresis), CEX (cation exchange), HILIC (hydrophilic interaction). This role may also perform additional testing such as TOC (total organic carbon), LAL (endotoxin testing), protein concentration, appearance and pH.
Under general supervision, this position is responsible for performing analytical testing and support in the HPLC/Capillary Electrophoresis (CE) group in Clinical Quality Control.
Responsibilities include
- Responsible for one or more of the following activities in QC: analytical testing, sample and data management and equipment maintenance.
- Perform routine laboratory procedures such as sample analysis, standard and solution preparation.
- Responsible for documenting, compiling, interpreting, reviewing and entering laboratory data.
- Providing and communicating results, maintaining/operating specialized equipment and drafting and revising documents such as Analytical Methods, SOPs and technical reports.
- Support introduction of new methods/techniques into the lab.
- Perform basic assay and instrument troubleshooting.
- May identify, recommend and implement improvements related to routine job functions.
- Must learn and align with safety guideline and basic cGMPs
- Must be flexible in working schedule as required
- Must be able to be on-call for CEMS as required
Pay and benefits
$63,000 – $85,000 a year
Employer provided62,571.90USD -84,656.10 USD
What you can expect of us
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.
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:
Apply now and make a lasting impact with the Amgen team.
Where you'll work
Thousand Oaks, CAOn-siteOpen in Maps (opens in a new tab)
More jobs in Thousand Oaks, CAWorking conditions
Career Category
Quality
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 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.
Equal opportunity, accessibility and legal noticesAmgen's statements, word for word
Amgen is an Equal Opportunity employer. We make all employment decisions without regard to race, color, religion, sex or any other characteristic protected by applicable law.
We provide reasonable accommodations to applicants and employees with disabilities, consistent with legal requirements. Please contact us to request accommodation.
Job intelligence
The context around this role
Live data · November 10, 2026
Salary intelligence
How the pay compares
This role's midpoint is 2% above the US median for Quality Control roles at this level.
This roleEmployer provided
Associate & Specialist roles in California15 roles publishing pay
Associate & Specialist roles in the US85 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $63,000 | — | $85,000 |
| California (middle half) | $63,250 | $64,000 | $75,500 |
| All US (middle half) | $64,000 | $72,500 | $88,500 |
This role: Amgen's own published range. Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, November 10, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 256 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not Amgen's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 28 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Lab testing and methods9
- Documentation and SOPs5
- Collaboration and leadership5
- GMP and compliance1
- Data and digital systems1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Quality Control work in biotechnology, led by the one this posting names, each linked to the agency or standards body that publishes it.
- FDA21 CFR Parts 210 and 211(official source, opens in a new tab)FDA current good manufacturing practice for finished pharmaceuticalsNamed in the posting
- USPUSP–NF(official source, opens in a new tab)US Pharmacopeia general chapters and monographs, such as <61> bioburden, <85> endotoxin, <1225> validation
- FDAFDA OOS guidance(official source, opens in a new tab)Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical Production
- FDAFDA data integrity guidance(official source, opens in a new tab)Data Integrity and Compliance With Drug CGMP: Questions and Answers
- ICHICH Q2(R2) and Q14(official source, opens in a new tab)Validation and development of analytical procedures
- FDAFDA analytical procedures guidance(official source, opens in a new tab)Analytical Procedures and Methods Validation for Drugs and Biologics
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- ICHICH Q1 stability testing(official source, opens in a new tab)Stability testing of drug substances and drug products
- EDQMEuropean Pharmacopoeia(official source, opens in a new tab)The Ph. Eur. quality standards for medicines in Europe, published by the EDQM
- ICHICH Q3 impurities(official source, opens in a new tab)Impurities in drug substances and products, residual solvents and elemental impurities
- FDAFDA aseptic processing guidance(official source, opens in a new tab)Sterile Drug Products Produced by Aseptic Processing: Current Good Manufacturing Practice
- ISOISO 14644-1(official source, opens in a new tab)Cleanroom air cleanliness classification by particle concentration
- EUEU GMP (EudraLex Volume 4)(official source, opens in a new tab)The EU's good manufacturing practice rules, including Annex 1 sterile and Annex 15 validation
- FDA21 CFR Parts 600 to 680(official source, opens in a new tab)FDA standards for biological products, from licensing to lot release
- ICHICH Q5 and Q6B(official source, opens in a new tab)Quality of biotechnological products and their specifications
- ISOISO/IEC 17025(official source, opens in a new tab)Competence of testing and calibration laboratories
Company hiring pulse
Amgen on Regulatory Jobs
- 59
- Open roles
- 59
- Distinct roles
- 5
- Locations
By discipline
- Quality35 58%
- Regulatory13 22%
- Clinical12 20%
By level
- Manager20 33%
- Senior & Principal19 32%
- Director13 22%
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Associate Quality Control HPLC/CE at Amgen
Open until filled. $63K–$85K a year, employer provided.