Job Description

40k - 45k

Boca Raton, FL - 100% onsite

Permanent

Responsibilities

• Create, format, revise and proofread controlled documents such as Standard Operating Procedures (SOPs), Forms, Validations, etc. from departments including but not limited to Quality Assurance, Manufacturing, Facilities, and Quality Control.
• Enforce limited access restrictions of secured controlled documents in the electronic and physical document locations.
• Process documents for approval signatures, official distribution, and absolution.
• Assist with maintaining inventory of on-site documentation.
• Assist with the maintenance of document retention and destruction schedules.
• Perform general office duties such as photocopying, word processing, filing, scanning, physical inventory, ordering supplies, etc.
• Proficient in cGMPs.
• Proficiency in computer systems requirements, validations, role and training assignments.
• Willingness to take on new projects.

Education Requirements :

High School diploma required.

Experience Requirements:

Minimum of one year of experience in the pharmaceutical or biotechnology industry and document management systems and software.

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