Regulatory Document Coordinator and Training Manager

Axle Informatics LLC

$90K — $100K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 5+ years of experience in regulatory documentation management
  • Strong understanding of federal regulations related to biosafety and aseptic processing
  • Proficient in managing document control systems and practices
  • Experience coordinating cross-functional teams for document reviews
  • Ability to track training compliance and generate detailed reports
  • Excellent writing and editing skills for SOPs and training modules
  • Strong organizational skills and attention to detail

Responsibilities

  • Manage lifecycle of SOPs, WIs, and Training Modules for APF and BSL operations
  • Coordinate periodic review cycles to ensure documents remain current
  • Facilitate approval processes, tracking status and deadlines
  • Oversee controlled distribution, ensuring only current documents are accessible
  • Monitor expiration timelines and initiate review processes proactively
  • Link training modules to supportive SOPs/WIs and track completion
  • Support internal and external audits by providing compliance documentation

Benefits

  • Health and wellness benefits including medical, dental, and vision
  • Retirement plan with employer contributions
  • Generous paid time off and holidays
  • Professional development opportunities
  • Flexible work arrangements and potential for hybrid schedules
Full Job Description
Regulatory Document Coordinator and Training Manager

Position Overview

This position provides critical support for federal-regulation-mandated documentation and quality control/assurance necessary to operate and maintain NIH's Aseptic Processing Facilities (APFs) and Biosafety Level (BSL) containment facilities. The Regulatory Document Coordinator and Training Manager will manage the full lifecycle of Standard Operating Procedures (SOPs), Work Instructions (WIs), and Training Modules for DFOM's APF and BSL operations - from initial drafting through periodic review, revision, approval routing, controlled distribution, and eventual retirement or archival. The role maintains detailed version control, authorship, revision history, and approval-status records within NIH's document control system, and monitors document expiration timelines to proactively trigger review or archival.

The position also coordinates cross-functional document reviews with relevant subject matter experts to verify content accuracy and alignment with DFOM policy and applicable regulatory and industry standards, and oversees controlled distribution so that only current, approved document versions remain accessible. In addition, the Coordinator tracks and manages personnel training status in direct linkage with the document control system - linking training modules to their supporting SOPs/WIs, monitoring completion against required timeframes, maintaining auditable training records, generating compliance reports, and supporting internal and external audits with documentation of employee qualifications and training adherence.

Deliverables
  • SOP/WI/Training Module Master Index & Status Log - Monthly / on-demand
  • New/Revised SOP, WI, and Training Module Drafts - As triggered by review cycle or business need
  • Document Review & Approval of Routing Records - Continuous, reported monthly
  • Document Expiration/Review Forecast Report - Monthly
  • Controlled Distribution Confirmation Records - Continuous
  • Personnel Training Status & Training Quiz/Assessment Report - Monthly
  • Quarterly Program Status Report - Quarterly
  • Annual Program Summary - Annually
  • QMS Account Management Report - Monthly

Statement of Work Details
  • Manage initial creation and drafting of new SOPs, Work Instructions, and Training Modules in accordance with DFOM templates and formatting standards
  • Coordinate periodic review cycles to ensure documents remain current and technically accurate
  • Manage the revision process, including tracking requested changes and incorporating approved edits
  • Facilitate the approval process, ensuring required approvers review and sign off within established timeframes
  • Manage distribution to ensure approved documents reach relevant personnel
  • Manage document retirement and expiration, including archival of superseded or obsolete documents
  • Utilize the NIH document control system to maintain detailed version control records for all SOPs, WIs, and Training Modules
  • Track authorship for each document and revision
  • Maintain complete revision history for each controlled document
  • Track approval status (pending, approved, rejected, returned for revision) for each document in the workflow
  • Record and monitor effective dates for all approved documents
  • Monitor document expiration timelines and proactively initiate review or archival processes as review/expiration dates approach
  • Coordinate cross-functional reviews involving relevant subject matter experts and stakeholders to ensure document accuracy
  • Verify that document content is consistent with current DFOM policies and procedures
  • Verify that document content aligns with applicable industry standards and regulatory requirements
  • Oversee controlled distribution processes to ensure only the most current, approved versions of documents are accessible to relevant personnel
  • Remove or restrict access to superseded or expired document versions
  • Link Training Modules to the specific SOPs and WIs they support
  • Track individual employee training status against required modules
  • Monitor to ensure all employees complete required training within designated timeframes
  • Maintain up-to-date, auditable training records for all applicable personnel
  • Generate compliance reports summarizing training completion status across DFOM/APF/BSL personnel
  • Support internal and external audits by providing documentation of employee qualifications and training adherence upon request


Disclaimer: The above description is meant to illustrate the general nature of work and level of effort being performed by individuals assigned to this position or job description. This is not restricted as a complete list of all skills, responsibilities, duties, and/or assignments required. Individuals may be required to perform duties outside of their position, job description or responsibilities as needed.

This role has a market-competitive salary with an anticipated base compensation range listed below. Actual salaries will vary depending on a candidate's experience, qualifications, skills, and location.

Salary Range

$90,000-$100,000 USD

Similar Jobs

More Jobs at Axle Informatics LLC

More Pharmaceuticals & Biotech Jobs

Find similar Regulatory Document Coordinator and Training Manager jobs: