Document Control Coordinator I (1st shift)

American Regent • New Albany, OH

4d • Onsite

About The Position

This position is a member of the Document Control Group, which is responsible for controlled documents associated with the manufacture of safe, pure, effective, and sterile pharmaceuticals in accordance with company SOPs, policies, and cGMPs. The Document Control Group provides support to other departments and is critical in maintaining production schedules and meeting company goals. The Document Control Coordinator will participate in all aspects of the Document Control Process, including all elements of the document lifecycle such as editing, reviewing, tracking, issuing, scanning, and filing of controlled documentation as per applicable Standard Operating Procedures. The Document Control Coordinator works under the direct supervision of senior management in Quality Assurance and senior members of the Document Control Group.

Requirements

• High School Diploma or GED equivalent required.
• Intermediate skills in Microsoft Word and Excel are required.
• Excellent organizational, interpersonal and communication skills (written and oral) required.
• Ability to take feedback constructively and function in a team oriented work environment.
• Ability to work overtime as needed.

Nice To Haves

• Associates or Bachelor’s Degree preferred.
• 0-1 year experience in Quality Assurance or Document Control function is preferred.
• Minimum 2 years work experience in a FDA regulated environment is preferred.
• Must be able to do work independently, recognizing what needs to be done and accomplishing it with minimal supervision.

Responsibilities

• Responsible for the revision and maintenance of controlled documents including Standard Operating Procedures, specifications, protocols, and other miscellaneous documents within the Electronic Document Management System (EDMS).
• Prepare controlled documents through the EDMS and change control process. This includes editing, proofreading, tracking, printing, scanning, and filing.
• Issue Master Batch Records to production in accordance with SOPs.
• Provide support for regulatory inspections and partner audits.
• Responsible for providing support to internal departments by requesting controlled copies, updating departments on periodic review, creating/sharing EDMS reports and reassigning tasks, as needed.
• Ensure all work is performed and documented in accordance with cGMP requirements and standard operating procedures.
• Able to perform tasks with minimal error rate.
• Provides training support regarding the EDMS for internal departments.
• Assist in Central Archive document intake, retrieval, and maintenance.
• Perform any other tasks/duties as assigned by management.

Benefits

• We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED