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Sr Associate QA Thousand Oaks CA
Job Location:
Job Location:
Thousand Oaks, CA - USA
Monthly Salary:
$ 111052 - 111052
Monthly Salary:
Posted:
26 July 2026 (30+ days ago)
Posted:
Application Deadline:
23 October 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
ATTENTION MILITARY AFFILIATED JOB SEEKERS- Our organization works with partner companies to source qualified talent for their open roles. The following position is available toVeterans Transitioning Military National Guard and Reserve Members Military Spouses Wounded Warriors and their Caregivers. If you have the required skill set education requirements and experience please click the submit button and follow the next steps. Unless specifically stated otherwise this role is On-Site at the location detailed in the job post.
Sr Associate Quality Assurance
What you will do
Lets do this. Lets change the this vital role you will be responsible to ensure that operations products are manufactured tested stored and distributed according to Good Manufacturing Practices (cGMP).
Supports and audits and inspections preparation planning execution and response activities as well as facilitating completion of compliance and regulatory requests
Provides QA oversight for IQA and ensures area readiness as the IQA compliance representative. Support IQA quality events change controls and risk assessments.
Supports ATO Management Review activities and metric control plan adherence
May perform review approval and tracking of cGMP processes procedures assays documents and records including but not limited to Nonconformances CAPAs Change Control records and validations. May also support execution of these tasks.
Collaborates cross functionally as needed to ensure the Quality Management System processes are executed in accordance with established procedures
Supports that facilities equipment materials organization processes procedures and products comply with cGMP practices and other applicable regulations
Supports Continual Improvement initiatives programs and projects
Alerts management of quality compliance supply and safety risks
Represents the Quality Assurance during audits and inspections
Completes required assigned training to permit execution of required tasks
Responsible for complying with Good Manufacturing Practices and Good Documentation Practices
What you will do
Lets do this. Lets change the this vital role you will be responsible to ensure that operations products are manufactured tested stored and distributed according to Good Manufacturing Practices (cGMP).
Supports and audits and inspections preparation planning execution and response activities as well as facilitating completion of compliance and regulatory requests
Provides QA oversight for IQA and ensures area readiness as the IQA compliance representative. Support IQA quality events change controls and risk assessments.
Supports ATO Management Review activities and metric control plan adherence
May perform review approval and tracking of cGMP processes procedures assays documents and records including but not limited to Nonconformances CAPAs Change Control records and validations. May also support execution of these tasks.
Collaborates cross functionally as needed to ensure the Quality Management System processes are executed in accordance with established procedures
Supports that facilities equipment materials organization processes procedures and products comply with cGMP practices and other applicable regulations
Supports Continual Improvement initiatives programs and projects
Alerts management of quality compliance supply and safety risks
Represents the Quality Assurance during audits and inspections
Completes required assigned training to permit execution of required tasks
Responsible for complying with Good Manufacturing Practices and Good Documentation Practices
Additional Qualifications/Responsibilities
What we expect of you
We are all different yet we all use our unique contributions to serve patients. The professional we seek is a leader with these qualifications.
Basic Qualifications:
High school/GED 4 years of Quality Assurance work experience
OR
Associates 2 years of Quality Assurance work experience
OR
Bachelors 6 months of Quality Assurance work experience
OR
Masters
Preferred Qualifications:
Demonstrated knowledge of current Good Manufacturing Practices (cGMP) Good Documentation Practices (GDP) and applicable regulations.
Experience with Quality Management System (QMS) processes
Knowledge of quality metrics Management Review processes and continuous improvement methodologies.
Experience supporting regulatory inspections partner audits and internal quality audits.
Experience serving as a Quality Assurance representative within a manufacturing or quality organization.
Excellent written and verbal communication skills including the ability to present information to leadership and regulatory inspectors.
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 well 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.
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.
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Salary Range
82081.95USD -111052.05 USD
Required Experience:
Senior IC
About Company
VetJobs & Military Spouse Jobs works with our employer partners to source, screen, and move qualified talent to the desktops of the Hiring Managers. Application is a two-step process, so please be patient with the team. When you submit to a position on our site your information will ... View more
