DOCUMENT CONTROL SPECIALIST

Adecco is assisting a local Client recruiting for Documentation Specialist. Irvine, CA.

If you meet the qualifications listed below – Apply Now!

Responsibilities for Maintaining the company’s-controlled documentation and records, implementing the advertising and promotional (ad-promo) materials process, supporting the change and document control process and records management activities.

Some of the Responsibilities include but are not limited to are:

  • Knowledge of FDA and ISO 13485 requirements are required.
  • Knowledge in Quality systems within medical device, pharmaceutical or other regulated industry is preferred.
  • Excellent attention to details, and organizational skills and interpersonal skills are required.
  • Proficient in Microsoft Office applications, Adobe Acrobat, and some knowledge of PLM and database applications are required.
  • Excellent written and oral communication skills are required.
  • Time management, critical thinking, and problem-solving skills are a must.
  • Associate degree or Equivalent Preferred.
  • Experience: Two years of experience in ad-promo/copy review or document control within a Medical Device Pharmaceutical or other regulated industry.

  • Apply with Adecco

Reference number US_EN_99_020076_1235760