Quality Assurance Associate

Los Angeles, CA

Post Date: 10/18/2017 Job ID: 93158 Industry: Distribution Pay Rate: $20/hour to $25/hour DOEE

 

 

 

 

Our client, a nutritional supplement distributor is looking for an experienced QA/QC Associate II to join their team!

 

QA/QC Associate II

 

This role will assist in the activities with development, application, and maintenance of quality standards for industrial processes.

Job Requirements:

  • BA/BS Degree in Chemistry or related discipline with 2 to 4 years' experience in a QA/QC environment or MS in Chemistry or related discipline and over 1 year experience in a QA/QC environment
  • Knowledge / Experience in cGMP and other pertinent regulations
  • cGMP and regulatory knowledge of relevant FDA and global stability guidelines
  • Excellent analytical and problem-solving skills and written and verbal communication
  • Experience with regulatory inspections would be advantageous
  • Ability to work in a fast pace environment and to value the importance of teamwork.

 

 

Job Duties Include:

The QA/QC Associate II is responsible for ensuring that all products are tested, approved and meet the established quality standard according to "The Code of Federal Regulations Title 21- Food and Drugs."

  • Provide support to the QA/QC, R&D, production department and technical support group.
  • Creates finished products, bulk products and raw material specification sheets in accordance with The Code of Federal Regulations Title 21 Food and Drugs 111.70.
  • Ensures the use of scientifically valid method for each established specification for which testing is required to determine whether the specification meets 111.320.
  • Reviews subset testing frequency in accordance with 21 CFR 111 and review and interpret  analytical data from third party testing labs and investigations of out-of-specification test results and assist with stability protocols and testing requirements necessary to establish product shelf-life.
  • Maintains the QA/QC laboratory invoices, purchase orders, and verifies testing charges for accuracy and for authorized signatures.
  • Assists the department with any tasks related to cGMP implementation and maintenance.
  • Coordinates with the Technical Support Department on the investigation of serious Adverse Event Reports, and other customer complaints.
  • Creates and revises SOP's, approves Material Reviews and Dispositions (MRD's) and change controls, as well as assists with any necessary training and implementation of QC procedures.

 

This is a full time temp to hire position that will be pay between $20/hour to $25/hour depending on education and experience. Hours are Monday to Friday 8-5pm.

Qualified candidates can submit their resume to la@stivers.com and refer to job # 93158 in the subject line . EOE/M/F/D/V.

 

 

 


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