Document Control Specialist - Quality Assurance

  • Location
    Torrance, California
  • Job type
  • Category
    Medical & Science - Pharmaceutical Preclinical Development

Document Control Specialist - Quality Assurance

Adecco Medical and Science providing services to the Pharmaceutical/ Biotech, Medical Device and OTC/Personal Care industry is currently seeking a Quality Assurance Document Control Specialist. Growing GMP laboratory has immediate opening for a QA Document Control Specialist. Responsibilities include maintaining and administering controlled document system, including standard operating procedures, test methods, forms, and supporting documents.

Job Summary: Administer routine QA activities directly related to data entry, issuing, editing, filing, and archiving of quality systems data and documentation. Works with the QA department for data archiving of documents including, but not limited to, SOP’s, forms, methods, notebooks and DCR’s.

Applicants must possess strong communication / organizational skills and ability to work as part of a team. Must be detail oriented multi-tasker and thrive in a fast paced environment. Proficient in use of Microsoft Word and Excel required. Familiarity with electronic document control system (CompliantPro) preferred. High School Diploma with two (2-3) years relevant experience.

If you are interested in this Quality Assurance Document Control Specialist job in Los Angeles, CA then please click APPLY NOW. For other opportunities available at Adecco Medical and Science go to If you have questions about the position or would like more information please contact Randy Williamson at 858-812-2601 or by email at

Equal Opportunity Employer Minorities/Women/Veterans/Disabled

  • Apply with Adecco

Reference number US_EN_2_108175_325650