Global Quality Docs & Change Analyst

Integrated Resources Inc.; Brea (CA); On-site; USD 80,000 - 110,000; Full time

Job summary

A leading company in workforce solutions seeks a Global Quality Systems Change Analyst to manage document control processes and ensure compliance with quality standards in the pharmaceutical or medical device industry. The role involves a range of responsibilities, including collaboration with teams, managing document edits, and ensuring adherence to regulatory requirements. Candidates must possess a scientific Bachelor's degree and relevant experience in document management within regulated environments.

Qualifications

• 3-5 years experience in document management in a regulated industry.
• Experience with 21 CFR 11, ISO 13485, ISO 9001.
• Self-starter with strong organizational skills.

Responsibilities

• Perform document control functions including change order management.
• Collaborate with cross-functional teams for document release.
• Review document content for internal process adherence.

Skills

Analytical

Verbal communication

Writing

Critical thinking

Problem-solving

Document management

Education

Bachelor’s degree in scientific discipline

Tools

Product Lifecycle Management (PLM) system

MS Office applications

Adobe Acrobat

Job description

A leading company in workforce solutions seeks a Global Quality Systems Change Analyst to manage document control processes and ensure compliance with quality standards in the pharmaceutical or medical device industry. The role involves a range of responsibilities, including collaboration with teams, managing document edits, and ensuring adherence to regulatory requirements. Candidates must possess a scientific Bachelor's degree and relevant experience in document management within regulated environments.