Document Control Specialist

Description

Job Purpose:

• Ability to learn and perform Document Control functions.
• Provide support for the Quality Management System.
• Create and maintain standard operating procedures, change control records, and documentation in accordance with cGMP while assisting as needed in any aspect of the document control process.
• Utilization of Laboratory Information Management System (Lab Vantage), SharePoint, and DOT Compliance software systems.
• Prepare and verify electronic and paper batch records.
• Requires copying, filing, and scanning.
• Organization and time management techniques using tools like Microsoft Outlook calendar, reminders, and task lists.
• Assists with additional work duties or responsibilities as evident or required.
• Flexibility to work overtime and weekends, if required.

• Route new and revised controlled documents (forms, master batch records, SOPs, test methods, work instructions, etc.) using DOT Compliance software systems.
• Assist with document accuracy including, but not limited to: formatting headers and footers, spelling corrections, appropriate grammar and punctuation, consistent fonts and numbering sequences, etc.
• Manage and maintain document archive process.
• Maintain original and working copy binders to ensure they contain the latest effective revisions.
• Maintain LIVE DOCs to ensure they contain the latest effective revisions.
• Update Master Distribution List and Table of Contents with current and approved document’s number, title, and effective date.
• Perform daily and quarterly audits to ensure the correct version of effective documents is in binders and used in preparing batch records.
• Assist with the preparation and verifying of batch records as demanded by the Production/Packaging
  
  Schedule:
• Review production schedule to determine what needs to be performed.
• Perform batch record generation for Nephron and 503B.
• Create batch IDs using Lab Vantage.
• Email and DOT system Activities
• Promptly respond to 8 - 20 request per day for emails and DOT Compliance.
• Promptly respond to email request including but not limited to:
  Logbook issuance and return process, Regulatory request, audit request, re-issuance, permissions, etc.
• Promptly respond to DOT Compliance request:
  Obsolete, grant permissions, implementation, etc.

• Copying, filing, and scanning of documents.
• Performs other similar duties as required.

• Technical background preferred, with knowledge of cGMP, and FDA regulations.
• Strong understanding of document control procedures, standards, and best practices
• Competent in Microsoft Word and Excel
• Knowledgeable in Adobe Acrobat (PDF) advanced features and workflows
• Familiar with document management software.
• Effective time management skills including prioritizing and scheduling.
• Effective communication and interpersonal abilities to work with cross-functional, fast-paced teams.
• Ability to prioritize tasks, manage time efficiently, and meet deadlines.
• Familiar with relevant industry regulations and compliance standards.
• Discretion in handling sensitive and confidential information.
• Strong critical thinking, analytical, problem-solving, and interpersonal skills
• Strong organizational skills with the ability to manage multiple projects or assignments simultaneously.

• Minimum of 1 year in the pharmaceutical industry preferred.
• 1-3 years of experience with Microsoft Word, Excel, and PowerPoint preferred.

• This position requires bending, typing, lifting (up to 40 1bs.), standing, sitting and walking throughout the facility.