Document Control Specialist
Quality Assurance

Reporting To:
Location: Hauppauge, NY

Responsibilities

  • Create batch records
  • Type and maintain all SOPs and forms
  • Maintain change control program
  • Maintain Corrective Action Preventative Action (CAPA) program
  • Circulate documents in a timely manner
  • Assist in document preparation and create streamlined approaches due to past experience
  • Provide and maintain user access to master documents
  • Maintenance of system including superseding outdated documents

Qualifications

  • Some college or a minimum of 2- 5 years experience in the pharmaceutical industry in QA or Document Control
  • Experience working in cGMPs
  • Computer software skills to include Outlook, Word and Excel
  • Excellent verbal and written communication skills with Spanish a plus
  • Effective organizational and analytical skills

CPC is offering a professional, stable work environment with excellent opportunity for career advancement in a dynamic company, a competitive salary and a comprehensive benefits package, which includes medical, dental, life insurance, paid time-off and 401(k) plan with matching contributions.

Apply Now!