×
Register Here to Apply for Jobs or Post Jobs. X
More jobs:

Sr Associate Quality Control

Job in West Greenwich, Kent County, Rhode Island, 02817, USA
Listing for: Amgen Inc. (IR)
Full Time position
Listed on 2026-02-14
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Location: West Greenwich

Sr Associate Quality Control page is loaded## Sr Associate Quality Controlremote type:
On Site locations:
US - Rhode Island - West Greenwich time type:
Full time posted on:
Posted 2 Days Agojob requisition :
R-236655##
** Career Category
** Operations## ##
** 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
**** What you will do
** Let’s do this. Let’s change the world. In this vital role you will complete and review analytical testing in our cGMP laboratory. The role will be on-site based out of Amgen Rhode Island and will work under the mentorship of the front-line manager. The Bioanalytics team provides analytical expertise in testing the following: in-process, release and stability samples. The laboratory employs a variety of test methodologies that use sophisticated equipment including: HPLC/UPLC, capillary electrophoresis and general chemistry methodologies such as:
Appearance, Color, Clarity, pH, Osmolality, Polysorbate, Protein Concentration, and Sub-Visible Particle testing.

Responsibilities include:

* Follow safety guidelines, cGMPs (Good Manufacturing Practices) and other applicable regulatory requirements
* Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks
* Ensures that facilities, equipment, materials, organization, processes, procedures and products follow cGMP practices and other applicable regulations
* Operate laboratory equipment and instrumentation
* Performs review and approval of assays, documents and records
* Supports Continual Improvement initiatives
* Alerts management of quality, compliance, supply and safety risks
* Participate in laboratory investigations
* Perform general laboratory housekeeping activities
* Completes required assigned training to permit carry through of required tasks
* Performs additional duties as specified by management
** What we expect of you
** We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek thrives in a fast paced environment and possesses these qualifications.
*
* Basic Qualifications:

*** High school diploma / GED and 4 years of Quality or Operations experience OR
* Associate’s degree and 2 years of Quality or Operations experience OR
* Bachelor’s degree and 6 months of Quality or Operations experience OR
* Master's degree
*
* Preferred Qualifications:

*** 1-2 years’ experience in HPLC/UPLC, capillary electrophoresis and general chemistry methodologies such as:
Appearance, Color, Clarity, pH, Osmolality, Polysorbate, Protein Concentration, and Sub-Visible Particle testing
* Demonstrated experience in laboratory investigations, method validation, audits, QC processes
* Ability to interpret scientific data
* Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal direction
* Strong communication skills (both written and oral), facilitation and presentation skills
* GMP/GDP experience
** 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…
Position Requirements
10+ Years work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary