Quality Assurance Documentation Specialist

Location: Riviera Beach, FL

Pay Rate: $16.00-$17.00 hourly

Working schedule: 1st shift

Description
The Document Control Specialist will be responsible for maintaining an organized and detailed
library of project documentation primarily using SharePoint. The Document Controls Specialist
will be responsible for the administration and control of documents that are received, created, or
issued as part of the QA project team.

Duties and Responsibilities

• Maintains, organizes, and updates documents in electronic drawing management systems.
• Familiarity with SharePoint preferred
• Complete administrative and analytical support in relation to QA document control services
• Demonstrates adherence to QA document services policies, procedures, standards, and guidelines
• Provides services for quality assurance document requests
• Communicates document requirements and client standards to the Sofgen Departments
• Performs collection, entry, and distribution procedures as required
• Ensures document transmittals by others are accurate and complete
• Utilizes interpersonal skills in maintaining balance with all party’s requirements and priorities
• Proactively communicates with QA staff and internal teams to manage workload and project requests
• Contributes to the development of department policies including documentation, storage, and organization policies
• Initiates corrective action for continuous improvement of efficiency and customer service
• Performs quality assurance and quality control of quality assurance documents
• Performs periodic archiving and audits to maintain document repository standards
• Investigates compliance as necessary.
• Support of quality documents with verification of document accuracy through audits
• Contributes to team effort by accomplishing related results as needed.

Education / Work Experience

• 2 years of previous document control experience in a quality assurance environment, or alike environment.
• Microsoft Office Applications Experience (i.e. Excel, Word, etc.)
• Strong communication and organization skills both verbal and written

Knowledge and Skills

• Demonstrated proficiency in analyzing data, problem identification and resolution, and ability to generate clear/concise reports indicating key issues
• High attention to detail
• Ability to interpret a variety of instructions furnished in written, and oral.
• Ability to work on multiple tasks and prioritize work
• Must be willing to work extended hours as necessary
• Ability to work cross-functionally as a team
• Strong PC and Microsoft Office skills
• Possess the skills and ability to coordinate, facilitate and participate in a collaborative approach for the completion of tasks and assignments.
• Actively participates as a member of the QA team to move forward with the completion of projects and goals.
• General understanding of basic quality assurance principles, FDA requirements
• Excellent understanding of department operating practices and procedures
• Excellent interpersonal, verbal, and written communication skills
• Flexibility to handle multiple tasks simultaneously in a competent and professional manner

Work Environment: GMP Manufacturing Environment