Captek Softgel International


QC Manager

Captek has three Southern California facilities


QC Manager

Cerritos Office

Summary: To oversee functions that impact product quality by monitoring compliance
to the Good Manufacturing practices. To manage quality control laboratory.

Duties and Responsibilities: 

  • Master current Good manufacturing practices and enforce compliance
  • Determines policies and procedures used in the QC laboratory
  •  Prepares raw material and finished product specification
  • Responsible for release or rejection of the raw material or finished product
  • Monitors, reviews and coordinates compliance to SOPs and GMPs, both in quality and manufacturing
  • Issue of the batch tickets and review of the batch production records for disposition
  • Trains manufacturing and Quality Assurance personnel in cGMPs and interacts with manufacturing managers
  • In charge of reviewing laboratory equipment for procurement
  • Hire and train technicians to operate laboratory equipment, sample and receive raw materials and to monitor production to ensure the finished product
    meets the product specification
  • Perform analytical tests plus review all analytical data. In-charge of the stability program
  • Develop and validate assay methods

Education, Training and work Experience Required: 

  • Bachelors degree in Science
  • Five years experience in dietary or pharmaceutical quality control
  • Experience in laboratory equipment operation

To apply:

If you are interested in this position, please apply here.