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Documentation Control Specialist

1 month ago

Sanford, Florida, United States ECLARO Full time

Job Title: Documentation Control Specialist

Job Summary: We are seeking a highly organized and detail-oriented Documentation Control Specialist to join our team at ECLARO. The successful candidate will be responsible for managing document control programs to ensure compliance with regulatory requirements.

Key Responsibilities:

• Maintain and control site documentation in electronic and paper systems to ensure compliance with cGMP.

• Audit and review assigned production documentation to ensure accuracy and reliability.

• Create and maintain Standard Operating Procedures (SOPs) for cGMP compliance programs.

• Manage site's electronic and paper document control systems to achieve cGMP compliance.

• Manage filing systems for current and archived documents required for cGMP compliance.

• Manage libraries of SOPs, Formulas, Manufacturing SOPs, Lab SPIs, and general SOPs to ensure accuracy and reliability.

Requirements:

• 1-3 years of industrial experience in FDA-regulated consumer products, pharmaceutical, or food industries.

• Self-driven, detail-oriented, and able to work independently on regularly scheduled tasks.

• Excellent ability to understand, read, speak, and write in English.

• Excellent interpersonal and communication skills.

• Strong multitasking skills and excellent time management skills.

• Working knowledge of Google Docs, Sheets, Slides, as well as Microsoft Word, Excel, and PowerPoint. SAP experience is a plus.