Skip navigation
Unable to save this job. Please try again later.


Email this Job to Yourself or a Friend

To begin the application process, please enter your email address.

Company Contact Info

Already have an account?

Sign in to apply with your saved resumes.

New to CareerBuilder?

Don't have an account? Continue as a guest!

Sorry, we cannot save or unsave this job right now.

Report this Job

Trust and Site Security Team.

Don't miss out on new jobs!

Get the latest Quality Control Specialist (Architecture and Engineering) jobs in San Francisco, CA delivered directly to your inbox. You can unsubscribe at any time.

Saving Your Job Alert

Job Alert Saved!

Could not save Job Alert!

You have too many Job Alerts!

This email address has reached the maximum of 5 email alerts. To create a new alert, you will need to log into your email and unsubscribe from at least one.

Sign Up

or   Sign In Here
Password Must Contain
8 to 15 characters
1 uppercase letter
1 number or symbol
1 lowercase letter
Create an Account with CareerBuilder to save jobs & unlock these great features
See similar job titles and skills to help you make your next move
Upload a resume and become visible to Hiring Managers and Employers
Compare Salary Information to see where you stand amongst your peers
Easily Quick Apply to jobs with just one click!

Email Send Failed!

Quality Systems Specialist (Contract)

EPM Scientific • San Francisco, CA

Posted 8 days ago

Job Snapshot

Degree - 4 Year Degree

Job Competition



How Do You Compare to the Competition?

Get facts about other applicants with a CareerBuilder Account

Job Description

Quality Systems Specialist (Contract)

One of the leading skincare companies in thee United States is looking to bring on a Quality Systems Specialist to their QA team in their South San Francisco office. The specialist will mainly be responsible for ensuring the Quality Documents, Validation reports, SOP's, Change Control, non-conformance, and document control are following cGMP regulations - and assisting in eQMS system development, validation, and launch activities.


  • Help generate, organize, manage and archive the cGMP documentation, investigation support documents, non-conformance, product release, CAPA, and stability program.
  • Work cross functionally within the organization to ensure the company is in compliance with applicable cGMP requirements and regulatory and Federal regulations.
  • Implement eQMS updates as needed to comply with applicable FDA compliance requirements
  • Provide training and access to the EQMS system which manages CAPAs, Change Controls and Deviations.
  • Review and approve documents for release as the QA SME.


  • Up to date cGMP requirements
  • 3+ years of experience in quality assurance
  • 1-2 years of quality systems experience
  • Prior experience in the skincare, pharmaceutical or manufacturing industry

Don't miss your chance to get your foot in the door at a company with proven success!

Job ID: 272601/001
Help us improve CareerBuilder by providing feedback about this job: Report this Job.
For your privacy and protection, when applying to a job online, never give your social security number to a prospective employer, provide credit card or bank account information, or perform any sort of monetary transaction. Learn more.
By applying to a job using CareerBuilder you are agreeing to comply with and be subject to the CareerBuilder Terms and Conditions for use of our website. To use our website, you must agree with the Terms and Conditions and both meet and comply with their provisions.
Don't miss out on new jobs like this
Get the latest jobs delivered to your inbox. Unsubscribe at any time.

Saving Your Job Alert

Job Alert Created

Well, this is embarrassing. We are having trouble saving your search. You can try again or come back at a later time.

Maximum Email Alerts

This email address has reached the maximum of 5 email alerts. To create a new alert, you will need to log into your email and unsubscribe from at least one.